WO1999005747A1 - In situ short-circuit protection system and method for high-energy electrochemical cells - Google Patents

In situ short-circuit protection system and method for high-energy electrochemical cells Download PDF

Info

Publication number
WO1999005747A1
WO1999005747A1 PCT/US1998/015299 US9815299W WO9905747A1 WO 1999005747 A1 WO1999005747 A1 WO 1999005747A1 US 9815299 W US9815299 W US 9815299W WO 9905747 A1 WO9905747 A1 WO 9905747A1
Authority
WO
WIPO (PCT)
Prior art keywords
cell
short
cells
temperature
circuited
Prior art date
Application number
PCT/US1998/015299
Other languages
French (fr)
Inventor
Michel Gauthier
Michael K. Domroese
Joseph A. Hoffman
David D. Lindeman
Joseph-Robert-Gaetan Noel
Vern E. Radewald
Jean Rouillard
Roger Rouillard
Toshimi Shiota
Jennifer L. Trice
Original Assignee
Minnesota Mining And Manufacturing Company
Hydro-Quebec Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Minnesota Mining And Manufacturing Company, Hydro-Quebec Corporation filed Critical Minnesota Mining And Manufacturing Company
Priority to EP19980935973 priority Critical patent/EP1021850A1/en
Priority to JP2000504628A priority patent/JP4267812B2/en
Priority to CA 2297839 priority patent/CA2297839C/en
Priority to AU85109/98A priority patent/AU8510998A/en
Publication of WO1999005747A1 publication Critical patent/WO1999005747A1/en

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/50Current conducting connections for cells or batteries
    • H01M50/572Means for preventing undesired use or discharge
    • H01M50/574Devices or arrangements for the interruption of current
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/60Heating or cooling; Temperature control
    • H01M10/61Types of temperature control
    • H01M10/613Cooling or keeping cold
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/60Heating or cooling; Temperature control
    • H01M10/64Heating or cooling; Temperature control characterised by the shape of the cells
    • H01M10/647Prismatic or flat cells, e.g. pouch cells
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/60Heating or cooling; Temperature control
    • H01M10/65Means for temperature control structurally associated with the cells
    • H01M10/655Solid structures for heat exchange or heat conduction
    • H01M10/6554Rods or plates
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Definitions

  • This invention relates generally to energy storage devices, and more particularly, to an apparatus and method for protecting energy storage cells upon occurrence of a short-circuit condition.
  • the thermal characteristics of an advanced battery cell must therefore be understood and appropriately considered when designing a battery system suitable for use in commercial and consumer devices and systems.
  • a conventional approach of providing a heat transfer mechanism external to such a cell may be inadequate to effectively dissipate heat from internal portions of the cell.
  • Such conventional approaches may also be too expensive or bulky in certain applications.
  • the severity of consequences resulting from short- circuit and thermal run-away conditions increases significantly when advanced high-energy electrochemical cells are implicated.
  • the present invention fulfills these and other needs.
  • the present invention is directed to an in-situ thermal management system for an energy storage device.
  • the energy storage device includes a plurality of energy storage cells each being coupled in parallel to common positive and negative connections.
  • Each of the energy storage cells in accordance with the cell's technology, dimensions, and thermal/electrical properties, is configured to have a ratio of energy content-to-contact surface area such that thermal energy produced by a short-circuit in a particular cell is conducted to adjacent and neighboring cells so as to prevent the temperature of the particular cell from exceeding a breakdown temperature.
  • a fuse is coupled in series with each of a number of energy storage cells.
  • the fuses are activated by a current spike capacitively produced by a cell upon occurrence of a short-circuit in the cell, thereby electrically isolating the short-circuited cell from the common positive and negative connections.
  • Figs. 1 A- IB illustrate an embodiment of a solid-state, thin-film electrochemical cell having a prismatic configuration and including a thermal conductor in accordance with an embodiment of the present invention
  • Fig. 1C is a partial illustration of an energy storing module containing a stack of thin-film electrochemical cells and employing an in-situ thermal management methodology in accordance with an embodiment of the present invention
  • Fig. 2 is a graphical representation of a relationship between voltage and capacity for an electrochemical cell of the type illustrated in Fig. 1;
  • Fig. 3 is an illustration of various film layers constituting a thin- film electrochemical cell
  • Fig. 4 illustrates various energy storage device configurations
  • Fig. 5 is an illustration of a grouping of energy storage cells subjected to a temperature increase due to a short-circuit condition in one of the cells;
  • Fig. 6 is a graphical representation of a relationship between maximum temperature of a cell under short-circuited conditions and normalized energy content of a cell, the graph providing ratios of energy content-to-contact surface area for adjacently disposed cells;
  • Figs. 7-9 illustrate various cell configurations that exhibit productive ratios of energy content-to-contact surface area
  • Fig. 10 shows an embodiment of a multiple-cell energy storage device in which one of the cells is subject to a short-circuit condition
  • Fig. 11 illustrate a relationship between the maximum temperature in a cell stack as a function of the number of adjacent short-circuited cells at five difference state of charge (SOC) levels;
  • Fig. 12 illustrates a characteristic current waveform for an electrochemical cell upon occurrence of a short-circuit in the cell
  • Fig. 13 is an embodiment of an integrated short-circuit protection device in accordance with an embodiment of the present invention
  • Fig. 14 is an exploded view of an energy storing module containing a number of interconnected thin-film electrochemical cells
  • Fig. 15 is a cross-sectional illustration of an embodiment of a pressure generating apparatus for maintaining a stack of electrochemical cells in a state of compression
  • Fig. 16 is an illustration of a band or strap including a tension producing clamp for use in a pressure generating apparatus for maintaining a stack of electrochemical cells in compression during charge and discharge cycling;
  • Fig. 17 is a perspective view of the tension producing clamp shown in Fig. 16;
  • Figs. 18-19 illustrate in a graphical form a relationship between maximum cell temperature of an energy storing module and the energy content and thickness of the cell, respectively.
  • the system includes solid-state, thin-film cells of the type shown in Fig. 1.
  • Such thin-film electrochemical cells are particularly well-suited for use in the construction of high-current, high- voltage energy storing modules and batteries, such as those used to power electric vehicles for example.
  • Fig. 1 A there is shown an embodiment of a prismatic electrochemical cell 50 which includes an anode contact 56 and a cathode contact 55 formed respectively along opposing edges of the electrochemical cell 50.
  • a thermal conductor 52 is spot welded or otherwise attached to each of the anode and cathode contacts 56, 55, respectively.
  • the thermal conductor 52 is typically disposed along the length of the anode contact 56 and the cathode contact 55, and typically includes an electrical connection lead 54 for conducting current into and out of the electrochemical cell 50, the current being collected and conducted preferentially along the anode and cathode contacts 56, 55.
  • the embodiment of a thermal conductor 63 shown in Fig. IB includes a copper tab 53 that extends along the length of a sprayed metal anode or cathode contact 61.
  • the copper tab 53 includes a resilient member 59 through which heat is transferred between the cell 50 and an adjacently disposed heat sink, such as a wall of a metallic housing.
  • the copper tab 53 is spot welded to the sprayed metal contact 61 at a number of weld locations 51.
  • a flexible electrical lead 57 is ultrasonically welded to the end 63 of the copper tab 53. Current is conducted primarily along the sprayed metal contact 61 of the cell 50 and communicated to external connections via the flexible electrical leads 57.
  • the thermal conductor 63 provides a thermal flux path for transferring thermal energy between the electrochemical cells and a thermally conductive, electrically resistive material or element.
  • a thermally conductive, electrically resistive material, element or structure as described herein refers to a surface coating/treatment or separate material that permits a sufficient amount of heat to be conducted therethrough, yet is electrically resistive to the flow of current relative to a current path provided for conducting current into and out of an electrochemical cell.
  • An anodized coating for example, may have a thickness that permits a sufficient amount of thermal energy to be conducted therethrough, yet is sufficiently resistive to electrical current relative to the anode and cathode contacts of the cell or the thermal conductor.
  • a thermally conductive polymer element may be employed, with the density of thermally conductive particles impregnated therein being selected to provide a desired balance between thermal and electrical conductivity characteristics.
  • the thermal conductors 63 also provide a thermal flux path for transferring heat between neighboring cells. If a short develops in a cell 73 within a stack of cells, for example, the excess heat, Q gen , generated by the short-circuited cell 73 is conducted through the thermally conductive, electrically resistive material provided on the housing surface 77, and to adjacent cells 72 and non-adjacent neighboring cells 71 via the thermal conductors 63. The excess heat, Q ger ⁇ , is also conducted to adjacent cells 72 in physical contact with the short-circuited cell 73.
  • a thermally conductive plate 75 serves as a heat sink for a cell 74 situated at the end of the cell stack.
  • the thermal conductor 63 is configured so as to exhibit a spring-like character which provides for substantially continuous contact between a cell 73 and a structure, such as a metallic planar surface 77, disposed adjacent the cell 73 in response to relative movement between the cell 73 and the adjacent structure 77.
  • a separate spring element, 69 such as a tubular elastomeric element, may be retained within the thermal conductor 63 to enhance the spring properties of the thermal conductor 63.
  • the thermal conductor 63 may be fashioned from copper and have a substantially C-shaped, double C-shaped, Z-shaped, O-shaped, S-shaped, V-shaped, or finger-shaped cross-section. In the embodiment shown in Fig.
  • the electrochemical cell 50 is fabricated to have a length L of approximately 135 mm, a height H of approximately 149 mm, and a width W ec of approximately 5.4 mm or approximately 5.86 mm when including a foam core element.
  • the width W c of the cathode contact 55 and the anode contact 56 is approximately 3.72 mm, respectively.
  • Such a cell 50 typically exhibits a nominal energy rating of approximately 36.5 Wh, a peak power rating of 87.0 W at 80 percent depth of discharge (DOD), and a cell capacity of 14.4 Ah at full charge.
  • Figure 2 illustrates in graphical form a relationship between voltage and capacity for an electrochemical cell having a construction substantially similar to that shown in Fig. 1 A. It can be seen that an individual electrochemical cell has a nominal operating voltage ranging between approximately 2.0 V and 3.1 V.
  • the electrochemical cells shown in Figs. 1A-1C may have a construction similar to that illustrated in Fig. 3.
  • an electrochemical cell 60 is shown as having a flat wound prismatic configuration which incorporates a solid polymer electrolyte 66 constituting an ion transporting membrane, a lithium metal anode 64, a vanadium oxide cathode 68, and a cathode current collector 70.
  • These film elements are fabricated to form a thin-film laminated prismatic structure, which may also include an insulation film, such as polypropylene film.
  • the cell shown in Fig. 3 includes a central cathode current collector 70 which is disposed between each of the two cathode films 68 to form a bi-face cell configuration.
  • a mono-face cell configuration may alternatively be employed in which a single cathode collector 70 is associated with a single anode/electrolyte/cathode element combination.
  • an insulating film is typically disposed between individual anode/electrolyte/cathode/collector element combinations.
  • a known sputtering metallization process is employed to form current collecting contacts along the edges 65, 79 of the anode and cathode current collecting films 64, 70, respectively. It is noted that the metal-sprayed contacts provide for superior current collection along the length of the anode and cathode film edges 65, 79, and demonstrate good electrical contact and heat transfer characteristics.
  • a number of electrochemical cells may be selectively interconnected in a parallel and/or series relationship to achieve a desired voltage and current rating.
  • a number of individual electrochemical cells 80 may be grouped together and connected in parallel to common positive and negative power buses or lines to form a cell pack 82.
  • a number of the electrochemical cell packs 82 may then be connected in series to form a module 84.
  • a number of individual modules 84 may be connected in series to constitute a battery 86.
  • FIG. 4 depicts an arrangement of electrochemical cells 80 in accordance with a modular packaging approach which provides an efficient means of achieving desired power requirements for a broad range of high-power applications.
  • eight electrochemical cells 80 are grouped together and connected in parallel to form a cell pack 82.
  • a module 84 is constituted by grouping six cell packs 82 together and connecting the packs 82 in series.
  • a battery 86 is shown as constituting 24 modules 84 connected in series. Given these arrangements, and assuming that each of the electrochemical cells 80 has dimensions and characteristics equivalent to those of the cell depicted in Fig. 1, each individual cell 80 provides for a total energy output of approximately 36.5 Wh.
  • Each cell pack 82 provides for a total energy output of approximately 292 Wh, while each module 84 provides for a total energy output of 1.75 kWh.
  • the battery 86 constituted by an array of four axially and six longitudinally oriented modules 84 connected in series, provides for a total energy output of approximately 42 kWh. It is understood that the arrangement of electrochemical cells 80 and interconnection of cells 80 forming a cell pack 82, module 84, and battery 86, may vary from the arrangements depicted in Fig. 4.
  • FIG. 5 there is shown a number of electrochemical cells arranged in a stack configuration.
  • a particular cell 112 is depicted as having sustained a short-circuit.
  • the cell 112 generates heat as a consequence of the high rate of energy discharge resulting from the short-circuit.
  • the thermal energy generated by the short-circuit in the cell 112 is partially conducted through the cell 112 and to the outer surfaces 115, 117 of the cell 112.
  • the close proximity of an adjacent cell 110 to the short-circuited cell 112 permits the thermal energy conducted to the outer surfaces 115, 117 of the cell 112 to dissipate into the adjacent cell 110.
  • an adjacent cell 114 having an outer surface 113 in thermal contact with an outer surface 117 of the cell 112, conducts heat produced by the cell 112 through the thermal contact interface 113, 117.
  • the adjacent cells 110, 114 include outer surfaces 111, 113 which are in intimate thermal contact with the outer surfaces 115, 117 of the cell
  • an insert element such as a foam or metallic flat spring element, or thermally conductive material, may be situated between adjacent cells.
  • an insert element such as a foam or metallic flat spring element, or thermally conductive material, may be situated between adjacent cells.
  • the heat generated by the short-circuited cell 112 is also conducted in the y and z directions and, in particular, to adjacent and neighboring cells via the thermal conductors and thermally conductive, electrically resistive material as is depicted in Fig. lC.
  • the energy increase within the short-circuited cell 112, and the rate at which the energy generated from the short-circuit event is dissipated into adjacent cells 110, 114 can be characterized through use of Fourier's Law of Heat Conduction.
  • a brief discussion of a generalized one-dimensional heat conduction analysis may be useful. It is understood that the following description is provided for purposes of illustration only, and ignores three- dimensional transient heat transfer considerations.
  • the rate at which heat flows axially through the short-circuited cell 112 is denoted as Q gen , which represents the heat generated per unit time in the cell 112 of thickness dx.
  • Q gen represents the heat generated per unit time in the cell 112 of thickness dx.
  • the quantity Q gen represents the heat energy generated throughout the volume element 118 which is dependent on the rate of heat generation per unit volume per unit time, represented by the parameter q, and the volume of the element 118.
  • the resulting energy balance equation is given by: Qx + Qgen - Qx+dx [1 ] and;
  • Q x , Q x+d x, and Q gen represent heat flow rates measured in watts (W)
  • q represents the rate of heat generation per unit volume per unit time measured in watts/m 3
  • dx represents the thickness of the volume element 118
  • A represents the cross-sectional area of the volume element 118.
  • An in-situ thermal management system in accordance with the principles of the present invention may be employed to dissipate excess thermal energy resulting from a short-circuit event without necessity of an external active thermal management scheme, such as a forced cooling or forced convection apparatus.
  • the in-situ thermal management methodology described herein may be implemented by understanding the heat capacity and heat dissipation characteristics of the particular cells used in an energy storage system, and appropriately limiting the energy content of the cells.
  • a cell having a construction of the type shown in Figs. 1 A-1C and 3 has a breakdown temperature of approximately 180° C, which represents the melting point of lithium.
  • Employment of an in-situ thermal management scheme implemented in accordance with the principles of the present invention prevents the temperature of a cell from reaching a breakdown temperature, or a safety temperature lower than the breakdown temperature, even under short-circuit conditions.
  • the heat dissipation characteristics of a particular cell are dependent on a number of factors, including the cell's technology, dimensions, and thermal/electrical properties. Taking into consideration these known factors, the heat dissipation characteristics of a cell may be altered and optimized. Since heat dissipation in the cell 112 is a function of thermal contact surface area with respect to contact surfaces of adjacent cells 110, 114, the maximum energy content per unit contact surface area required to maintain the cell temperature below a breakdown or safety temperature may be determined. By way of example, and with reference to Fig. 6, there is shown in graphical form a relationship between the maximum temperature of a cell having a construction as shown in Figs.
  • the energy content of a cell and the physical dimensions of the cell may be selected so that the ratio of energy content-to-cell surface area is kept within a range such that the maximum cell temperature remains below a breakdown or safety temperature, even under short- circuit conditions.
  • An energy content-to-contact surface area ratio of less than approximately 0.0050 Wh/cm for a thin-film lithium polymer cell will ensure that a worst-case temperature resulting from a short-circuit in the cell does not exceed the melting point of the lithium elements within the cell (i.e., 180° C).
  • the energy content and contact surface area of the cell may be appropriately selected using the graph of Fig. 6. It is understood that graphs similar to that shown in Fig. 6 which characterize maximum cell temperature under short- circuit conditions relative to the ratio of energy content-to-contact surface area may be developed for energy storage cells constructed using technologies other than those described herein. It is noted that Fig. 18, for example, depicts a relationship between energy content and maximum cell temperature for a cell having a similar construction as that shown in Figs. 1A-1C and 3 but a different cathode oxide.
  • Figs. 7-9 The depictions of energy storage cells shown in Figs. 7-9 are provided to illustrate that an in-situ thermal management design approach may be employed for energy storage cells having varying configurations.
  • the length (L), height (H), width (w), or radius (r) may be varied as needed for a given application, with the constraint that the ratio of energy content-to-contact surface area remain in a range that prevents the worst-case cell temperature from exceeding the cell breakdown temperature.
  • Equation [3] mathematically characterizes the maximum cell temperature of a thin-filmed electrochemical cell, which does not include a foam core element, as a function of various operative parameters.
  • the dimensions of the cell characterized in Equation [3] are given as 0.135m x 0.149m x 0.054m.
  • the maximum cell temperature for the cell is given by:
  • T max 1/1.1-1/1.2.0.037738.(l/( PcelI .Cp cell ))° 385s -(Q/kcell) • ( ⁇ ) 06146 • (K/L) "0077 [3]
  • T max represents the maximum temperature reached by a short-circuited cell in a module (° C)
  • p ce ⁇ represents the density of the cell (kg/m 3 )
  • Cp ce ⁇ represents the heat capacity of the cell (J/kgK)
  • Q represents the energy content of one cell per unit volume (Wh/m )
  • kcell represents the conductivity of the cell in the cell-to-cell axial direction (W/mK)
  • represents cell thickness in the cell- to-cell axial direction (mm)
  • K L represents the conductance of the thermal conductor (W/m 2 K).
  • Equation [3] above a relationship between maximum temperature of a short-circuited cell as a function of the cell's energy content for a given cell chemistry and configuration may be developed.
  • a relationship between maximum cell temperature as a function of cell thickness may also be developed.
  • Figs. 18-19 there is depicted a relationship between maximum cell temperature as a function of energy content and cell thickness, respectively.
  • a thin-film electrochemical cell of the type characterized above should have an energy content which is limited to less than approximately 38 Wh to ensure that the maximum temperature of the cell will not exceed a breakdown temperature, such as the melting point of lithium (i.e., 180° C). It is interesting to note the linearity of the maximum cell temperature-to-energy content relationship depicted in Figs. 18 and 6, given the difference in cell technology. It can be seen from Fig. 19 that the thickness of the cell should not exceed approximately 8.5 mm in order to ensure that the maximum temperature of the cell does not exceed the 180° C breakdown temperature.
  • Equation [4] characterizes maximum cell temperature for an energy storing module of the same cell technology as that implicated in Equation [3] in which some of the cells include a foam core element compressed to approximately 2 mm. More specifically, Equation [4] characterizes maximum cell temperature for a module design in which compressed foam core elements are provided in every two electrochemical cells. In this case, maximum cell temperature for such a module configuration is given by:
  • Equation [3] and [4] differ only by constants (i.e., the constants 1/1.1 and 1/1.2 in Equation [3]).
  • Equation [5] characterizes the maximum cell temperature for a module having cells of the same technology implicated in Equations [3]-[4], wherein the cells incorporate a foam core element that is thinner than the element associated with Equation [4] above. More specifically, Equation [5] below assumes that a foam core element having a thickness of approximately 1/32 inches is provided in every two cells of the cell stack. The foam core element is fabricated from Poron S2000. The maximum cell temperature for a module having this configuration is given by:
  • T max 1/1.1 . 0.037738 • (l/( Pce Harbor • Cp cel ,)) 3856 • (Q/kcell) • ( ⁇ ) 06146 • (K/L) "0077 [5]
  • Equations [3]-[5] may be used to quantify the effect of heat capacity of the components within the cell on the maximum cell temperature, T max , reached during a short-circuit event. These equations, therefore, may be used to characterize maximum cell temperatures under similar situations for energy storing cells of differing technologies.
  • Equations [3]-[5] were directed to the investigation of electrochemical cells having an energy content that varied from approximately 30 to 40 Wh, a cell thickness, ⁇ , that varies from approximately 5.4 and 7.8 mm, and cells that utilize a thermal conductor having a conductance value, K/L, that varies between approximately 200 and 600
  • the in-situ thermal management approach described above with reference to Figs. 1C and 5 is generally applicable for managing short-circuit temperature increases occurring in a single cell of a grouping of cells.
  • an enhanced in-situ short-circuit protection scheme may be implemented to prevent thermal runaway within the cell stack, and to isolate a particular cell from the parallel connection upon occurrence of a short-circuit in the cell.
  • the energy storage device 120 includes eight energy storage cells respectively connected in parallel to common positive and negative terminals
  • the cell EC1 is shown as a short-circuit. Given this arrangement, and with reference to Fig. 11, it can be seen that only one short-circuited cell within a stack of eight cells can be managed using the above-described in-situ thermal management methodology without exceeding the breakdown temperature of the cell material.
  • An in-situ short-circuit protection device may be incorporated into an energy storage system to prevent multiple short-circuit events from occurring.
  • a fuse 123 is connected in series with a respective cell 122 within the multiple-cell energy storage device 120.
  • the fuse 123 of the defective cell 122 blows so as to electrically isolate the short-circuited cell 122 from the parallel connection.
  • the heat generated during development of the short-circuit in the cell 122 and after blowing of the fuse 123 is conducted to cells adjacent the defective cell 122 in a manner previously described.
  • the maximum temperature attainable by a cell under worst-case conditions is well below the breakdown temperature of the cell. More particularly, the data of Fig. 11 confirms that the temperature of a short-circuited cell within the cell stack never exceeds a safety temperature of 130° C when an in-situ short-circuit protection device is employed. Referring now to Fig.
  • FIG. 12 there is illustrated a graph which characterizes the effect on cell current upon the occurrence of a short-circuit in a thin-film electrochemical cell.
  • the current in the cell characterized in Fig. 12 spikes at a value in excess of 500 A in less than approximately 100 milliseconds. Following the current spike, the current in the cell rapidly decays to approximately 150 A after 1 second, and gradually decays thereafter. At 5 seconds following the short- circuit event, the cell current reaches a value of approximately 60 A.
  • each of the fuses 123 connected in series with a corresponding energy storage cell 122 are designed to activate in response to a current spike generated from a short- circuit in the cell 122.
  • a fuse 123 typically has a current rating that prevents the fuse from activating during normal operation, yet permits the fuse to activate in response to a short-circuit condition.
  • the parallel connected cells of an energy storage device have a structure and behavior similar to those previously described with reference to Figs. 1A-1C and 3.
  • the fuses connected in series with the cells have a current rating of approximately 50 A.
  • protection against accidental shorting of an energy storage device or cell may be of primary concern. It may be desirable, therefore, to employ a fuse that is activated more slowly than the fast acting fuse described above. For example, a fuse that activates after several hundred milliseconds or several seconds after occurrence of a short-circuit in the cell may be employed. Although excess heat is generated between the time the short occurs and the time the fuse blows, the in-situ thermal management methodology described previously provides for the safe dissipation of such excess heat.
  • FIG. 13 there is illustrated an embodiment of a short-circuit protection device fabricated in an integrated package.
  • the integrated device 130 includes an enclosure 132 within which eight fuses (not shown) are mounted. A first contact of each fuse is connected in series with a corresponding one of eight terminals 134, and a second contact of the each fuse is connected to a common bus 140.
  • Each of the terminals 134 includes a lead 136 and a contact 138.
  • each of the contacts 138 engages a corresponding contact of one of eight cells in the array.
  • the common bus 140 is typically coupled to one or more common busses of other short-circuit protection devices 130 connected to corresponding cell arrays to form a series connected energy storage device, such as a module.
  • the enclosure 132 has a height, H E , of 16.00 mm, a width, W E , of 7.49 mm, and a length, L E , of 50.80 mm.
  • the lead portion 136 of the terminal 134 has a height, H L , of 12.70 mm, a width, W L , of 1.27 mm, and a length, L L , of 5.00 mm.
  • the contact portion 138 of the terminal 134 has a height, He, and a width, Wc, of 1.27 mm, and a length, L c , of 13.03 mm.
  • the common bus 140 has a height, HCB, of 6.35 mm, a width, W CB , of 1.27 mm, and a length, L CB , of 49.02 mm.
  • Fig.14 there is shown an exploded view of an embodiment of an energy storing module 142 which houses a number of electrochemical cells 144, interconnection hardware, and control hardware and software.
  • the module 142 includes a stack of 48 electrochemical cells 144 which are interconnected through use of a interconnect board 147.
  • Short-circuit protection circuitry such as an integrated short-circuit protection pack 148, is typically provided on the interconnect board 147.
  • Each of the six integrated short-circuit protection packs 148 disposed on the interconnect board 147 electrically couple to a corresponding one of six cell packs 143 upon mounting the interconnect board 147 in place above the stack of cells 144.
  • the volume of an electrochemical cell of the type described previously with regard to Fig. 1 varies during charge and discharge cycling due to the migration of lithium ions into and out of the lattice structure of the cathode material. This migration creates a corresponding increase and decrease in total cell volume on the order of approximately five to six percent during charging and discharging, respectively.
  • a pressure producing apparatus is employed to maintain the cells in a continuous state of compression to ensure continuous intimate contact between cell of the cell stack. It is considered desirable that the compressive forces, whether produced internally or externally of the cell, be distributed fairly uniformly over the surface of application.
  • the stack of electrochemical cells 144 shown in Fig. 14 are banded together by use of two bands 146 and two opposing thrust plates 145.
  • the 48 electrochemical cells 144 are subjected to continuous compressive forces generated by use of the bands 146/thrust plates 145 and a foam or spring-type element disposed in each of the cells 144 and/or between all or selected ones of the cells 144.
  • the foam or spring-type core element provided in the center of each of the cells 144 serves to distribute pressure evenly between the cells 144, which is of particular importance as cell volumes change during charge and discharge cycling.
  • a metal strap 194 includes a wave-like spring 198 which generates tension forces that cause the thrust plates 194, in turn, to exert compressive forces on the cell stack 192.
  • the tension spring apparatus illustrated in Fig. 15 may be implemented using a number of coil springs or using elastomeric material, and that a combination of metallic and elastomeric spring materials may also be advantageously employed. Further, it will be appreciated that foam or other spring elements may be incorporated within the cell stack and/or within individual cells in combination with a tension spring apparatus external to cell stack.
  • FIG. 16 illustrates an embodiment of a strap apparatus 180 which is particularly useful in constraining a number of electrochemical cells configured as a stack or bundle.
  • the strap apparatus shown in Fig. 16 incorporates a unique clamp 182 which significantly enhances the efficacy of a cell stack pressure system.
  • the strap apparatus includes two bands 180 each having C-shaped ends 181.
  • a clamp 182 is attached to a band 180 by coupling the C-shaped ends 181 of the band 180 with corresponding C-shaped ends 184 of the clamp 182. It is assumed that the bands 180 are disposed around the stack of cells in a manner as shown in Fig. 15.
  • the clamp 182 includes a hinge 186 integral to the clamp 182 which is collapsible onto a contact surface 188 of the clamp 182 when subjected to sufficient force.
  • the C-shaped ends 184 of the clamp 182 are pulled towards each other which, in turn, produces a tension force in the C-shaped ends of the bands 180.
  • the magnitude of the tension force induced in the bands 180 by actuation of the clamps 182 is moderated by a sign wave-shaped spring 189 integral to the clamps 182.
  • the sign wave-shaped spring 189 may be configured, in terms of shape, thickness, and material, to provide for a desired amount of expansion and retraction of the strap apparatus during charge/discharge cycling of the cells.
  • a short-circuit protection device may include thermally activated fuses, such as Model NTE8090 manufactured by NTE Electronics, rather those described herein.
  • Thermally activated fuses typically activate at a prescribed temperature, such as a temperature below a breakdown temperature.
  • a thermally activated fuse may be connected in series with a current activated fuse which provides for increased activation reliability.
  • the principles of the present invention may be employed for use with battery technologies other than those exploiting lithium polymer electrolytes, such as those employing nickel metal hydride (Ni-MH), lithium-ion, (Li-Ion), and other high energy battery technologies. Accordingly, the scope of the present invention should not be limited by the particular embodiments discussed above, but should be defined only by the claims set forth below and equivalents thereof.

Abstract

An in situ thermal management system for an energy storage device. The energy storage device includes a plurality of energy storage cells each being coupled in parallel to common positive and negative connections. Each of the energy storage cells, in accordance with the cell's technology, dimensions, and thermal/electrical properties, is configured to have a ratio of energy content-to-contact surface area such that thermal energy produced by a short-circuit in a particular cell is conducted to a cell adjacent the particular cell so as to prevent the temperature of the particular cell from exceeding a breakdown temperature. In one embodiment, a fuse is coupled in series with each of a number of energy storage cells. The fuses are activated by a current spike capacitively produced by a cell upon occurrence of a short-circuit in the cell, thereby electrically isolating the short-circuited cell from the common positive and negative connections.

Description

IN-SITU SHORT-CIRCUIT PROTECTION SYSTEM AND METHOD FOR HIGH-ENERGY ELECTROCHEMICAL CELLS
FIELD OF THE INVENTION
This invention relates generally to energy storage devices, and more particularly, to an apparatus and method for protecting energy storage cells upon occurrence of a short-circuit condition.
BACKGROUND OF THE INVENTION
The demand for new and improved electronic and electromechanical systems has placed increased pressure on the manufacturers of energy storage devices to develop battery technologies that provide for high energy generation in a low-volume package. Conventional battery systems, such as those that utilize lead acid for example, are often unsuitable for use in high- power, low-weight applications. Other known battery technologies may be considered too unstable or hazardous for use in consumer product applications. A number of advanced battery technologies have recently been developed, such as metal hydride (e.g., Ni-MH), lithium-ion, and lithium polymer cell technology, which would appear to provide the requisite level of energy production and safety margins for many commercial and consumer applications. Such advanced energy storage systems, however, typically produce a significant amount of heat which, if not properly dissipated, can result in a thermal runaway condition and eventual destruction of the cells, as well as the system being powered by the cells.
The thermal characteristics of an advanced battery cell must therefore be understood and appropriately considered when designing a battery system suitable for use in commercial and consumer devices and systems. A conventional approach of providing a heat transfer mechanism external to such a cell, for example, may be inadequate to effectively dissipate heat from internal portions of the cell. Such conventional approaches may also be too expensive or bulky in certain applications. The severity of consequences resulting from short- circuit and thermal run-away conditions increases significantly when advanced high-energy electrochemical cells are implicated. There is a need in the advanced battery manufacturing industry for an energy storage system that exhibits high-energy output, and one that provides for safe and reliable use in a wide range of applications. There exists a further need for a non-intrusive, inexpensive thermal management approach that protects energy storage cells from thermal run-away resulting from a short- circuit condition. The present invention fulfills these and other needs.
SUMMARY OF THE INVENTION
The present invention is directed to an in-situ thermal management system for an energy storage device. The energy storage device includes a plurality of energy storage cells each being coupled in parallel to common positive and negative connections. Each of the energy storage cells, in accordance with the cell's technology, dimensions, and thermal/electrical properties, is configured to have a ratio of energy content-to-contact surface area such that thermal energy produced by a short-circuit in a particular cell is conducted to adjacent and neighboring cells so as to prevent the temperature of the particular cell from exceeding a breakdown temperature. In one embodiment, a fuse is coupled in series with each of a number of energy storage cells. The fuses are activated by a current spike capacitively produced by a cell upon occurrence of a short-circuit in the cell, thereby electrically isolating the short-circuited cell from the common positive and negative connections. BRIEF DESCRIPTION OF THE DRAWINGS
Figs. 1 A- IB illustrate an embodiment of a solid-state, thin-film electrochemical cell having a prismatic configuration and including a thermal conductor in accordance with an embodiment of the present invention;
Fig. 1C is a partial illustration of an energy storing module containing a stack of thin-film electrochemical cells and employing an in-situ thermal management methodology in accordance with an embodiment of the present invention; Fig. 2 is a graphical representation of a relationship between voltage and capacity for an electrochemical cell of the type illustrated in Fig. 1;
Fig. 3 is an illustration of various film layers constituting a thin- film electrochemical cell;
Fig. 4 illustrates various energy storage device configurations; Fig. 5 is an illustration of a grouping of energy storage cells subjected to a temperature increase due to a short-circuit condition in one of the cells;
Fig. 6 is a graphical representation of a relationship between maximum temperature of a cell under short-circuited conditions and normalized energy content of a cell, the graph providing ratios of energy content-to-contact surface area for adjacently disposed cells;
Figs. 7-9 illustrate various cell configurations that exhibit productive ratios of energy content-to-contact surface area;
Fig. 10 shows an embodiment of a multiple-cell energy storage device in which one of the cells is subject to a short-circuit condition;
Fig. 11 illustrate a relationship between the maximum temperature in a cell stack as a function of the number of adjacent short-circuited cells at five difference state of charge (SOC) levels;
Fig. 12 illustrates a characteristic current waveform for an electrochemical cell upon occurrence of a short-circuit in the cell;
Fig. 13 is an embodiment of an integrated short-circuit protection device in accordance with an embodiment of the present invention; Fig. 14 is an exploded view of an energy storing module containing a number of interconnected thin-film electrochemical cells;
Fig. 15 is a cross-sectional illustration of an embodiment of a pressure generating apparatus for maintaining a stack of electrochemical cells in a state of compression;
Fig. 16 is an illustration of a band or strap including a tension producing clamp for use in a pressure generating apparatus for maintaining a stack of electrochemical cells in compression during charge and discharge cycling; Fig. 17 is a perspective view of the tension producing clamp shown in Fig. 16; and
Figs. 18-19 illustrate in a graphical form a relationship between maximum cell temperature of an energy storing module and the energy content and thickness of the cell, respectively.
DETAILED DESCRIPTION OF THE EMBODIMENTS
In accordance with one embodiment of an energy storage system that utilizes high-energy electrochemical cells, the system includes solid-state, thin-film cells of the type shown in Fig. 1. Such thin-film electrochemical cells are particularly well-suited for use in the construction of high-current, high- voltage energy storing modules and batteries, such as those used to power electric vehicles for example. In Fig. 1 A, there is shown an embodiment of a prismatic electrochemical cell 50 which includes an anode contact 56 and a cathode contact 55 formed respectively along opposing edges of the electrochemical cell 50. A thermal conductor 52 is spot welded or otherwise attached to each of the anode and cathode contacts 56, 55, respectively. The thermal conductor 52 is typically disposed along the length of the anode contact 56 and the cathode contact 55, and typically includes an electrical connection lead 54 for conducting current into and out of the electrochemical cell 50, the current being collected and conducted preferentially along the anode and cathode contacts 56, 55.
The embodiment of a thermal conductor 63 shown in Fig. IB includes a copper tab 53 that extends along the length of a sprayed metal anode or cathode contact 61. The copper tab 53 includes a resilient member 59 through which heat is transferred between the cell 50 and an adjacently disposed heat sink, such as a wall of a metallic housing. The copper tab 53 is spot welded to the sprayed metal contact 61 at a number of weld locations 51. A flexible electrical lead 57 is ultrasonically welded to the end 63 of the copper tab 53. Current is conducted primarily along the sprayed metal contact 61 of the cell 50 and communicated to external connections via the flexible electrical leads 57.
As is shown in Fig. 1C, the thermal conductor 63 provides a thermal flux path for transferring thermal energy between the electrochemical cells and a thermally conductive, electrically resistive material or element. It is to be understood that a thermally conductive, electrically resistive material, element or structure as described herein refers to a surface coating/treatment or separate material that permits a sufficient amount of heat to be conducted therethrough, yet is electrically resistive to the flow of current relative to a current path provided for conducting current into and out of an electrochemical cell. An anodized coating, for example, may have a thickness that permits a sufficient amount of thermal energy to be conducted therethrough, yet is sufficiently resistive to electrical current relative to the anode and cathode contacts of the cell or the thermal conductor. By way of further example, a thermally conductive polymer element may be employed, with the density of thermally conductive particles impregnated therein being selected to provide a desired balance between thermal and electrical conductivity characteristics.
As is further shown in the multiple cell embodiment of Fig. 1C, the thermal conductors 63 also provide a thermal flux path for transferring heat between neighboring cells. If a short develops in a cell 73 within a stack of cells, for example, the excess heat, Qgen, generated by the short-circuited cell 73 is conducted through the thermally conductive, electrically resistive material provided on the housing surface 77, and to adjacent cells 72 and non-adjacent neighboring cells 71 via the thermal conductors 63. The excess heat, Qgerι, is also conducted to adjacent cells 72 in physical contact with the short-circuited cell 73. A thermally conductive plate 75 serves as a heat sink for a cell 74 situated at the end of the cell stack. Further, the thermal conductor 63 is configured so as to exhibit a spring-like character which provides for substantially continuous contact between a cell 73 and a structure, such as a metallic planar surface 77, disposed adjacent the cell 73 in response to relative movement between the cell 73 and the adjacent structure 77. A separate spring element, 69, such as a tubular elastomeric element, may be retained within the thermal conductor 63 to enhance the spring properties of the thermal conductor 63. The thermal conductor 63 may be fashioned from copper and have a substantially C-shaped, double C-shaped, Z-shaped, O-shaped, S-shaped, V-shaped, or finger-shaped cross-section. In the embodiment shown in Fig. 1 A, the electrochemical cell 50 is fabricated to have a length L of approximately 135 mm, a height H of approximately 149 mm, and a width Wec of approximately 5.4 mm or approximately 5.86 mm when including a foam core element. The width Wc of the cathode contact 55 and the anode contact 56 is approximately 3.72 mm, respectively. Such a cell 50 typically exhibits a nominal energy rating of approximately 36.5 Wh, a peak power rating of 87.0 W at 80 percent depth of discharge (DOD), and a cell capacity of 14.4 Ah at full charge. Figure 2 illustrates in graphical form a relationship between voltage and capacity for an electrochemical cell having a construction substantially similar to that shown in Fig. 1 A. It can be seen that an individual electrochemical cell has a nominal operating voltage ranging between approximately 2.0 V and 3.1 V.
The electrochemical cells shown in Figs. 1A-1C may have a construction similar to that illustrated in Fig. 3. In this embodiment, an electrochemical cell 60 is shown as having a flat wound prismatic configuration which incorporates a solid polymer electrolyte 66 constituting an ion transporting membrane, a lithium metal anode 64, a vanadium oxide cathode 68, and a cathode current collector 70. These film elements are fabricated to form a thin-film laminated prismatic structure, which may also include an insulation film, such as polypropylene film.
The cell shown in Fig. 3 includes a central cathode current collector 70 which is disposed between each of the two cathode films 68 to form a bi-face cell configuration. A mono-face cell configuration may alternatively be employed in which a single cathode collector 70 is associated with a single anode/electrolyte/cathode element combination. In this configuration, an insulating film is typically disposed between individual anode/electrolyte/cathode/collector element combinations. A known sputtering metallization process is employed to form current collecting contacts along the edges 65, 79 of the anode and cathode current collecting films 64, 70, respectively. It is noted that the metal-sprayed contacts provide for superior current collection along the length of the anode and cathode film edges 65, 79, and demonstrate good electrical contact and heat transfer characteristics. The electrochemical cells illustrated in Figs. 1A-1C and
3 may be fabricated in accordance with the methodologies disclosed in U.S.
Patent Nos. 5,423,110, 5,415,954, and 4,897,917.
In Table 1 below, various thermal properties are provided for an electrochemical cell having a construction similar to that illustrated in Fig. 1 and maintained at a temperature of approximately 60° C.
TABLE 1
Figure imgf000010_0001
A number of electrochemical cells may be selectively interconnected in a parallel and/or series relationship to achieve a desired voltage and current rating. For example, and with reference to Fig. 4, a number of individual electrochemical cells 80 may be grouped together and connected in parallel to common positive and negative power buses or lines to form a cell pack 82. A number of the electrochemical cell packs 82 may then be connected in series to form a module 84. Further, a number of individual modules 84 may be connected in series to constitute a battery 86.
The embodiment shown in Fig. 4 depicts an arrangement of electrochemical cells 80 in accordance with a modular packaging approach which provides an efficient means of achieving desired power requirements for a broad range of high-power applications. In this illustrative embodiment, eight electrochemical cells 80 are grouped together and connected in parallel to form a cell pack 82. A module 84 is constituted by grouping six cell packs 82 together and connecting the packs 82 in series. A battery 86 is shown as constituting 24 modules 84 connected in series. Given these arrangements, and assuming that each of the electrochemical cells 80 has dimensions and characteristics equivalent to those of the cell depicted in Fig. 1, each individual cell 80 provides for a total energy output of approximately 36.5 Wh. Each cell pack 82 provides for a total energy output of approximately 292 Wh, while each module 84 provides for a total energy output of 1.75 kWh. The battery 86, constituted by an array of four axially and six longitudinally oriented modules 84 connected in series, provides for a total energy output of approximately 42 kWh. It is understood that the arrangement of electrochemical cells 80 and interconnection of cells 80 forming a cell pack 82, module 84, and battery 86, may vary from the arrangements depicted in Fig. 4.
In Fig. 5, there is shown a number of electrochemical cells arranged in a stack configuration. A particular cell 112 is depicted as having sustained a short-circuit. The cell 112 generates heat as a consequence of the high rate of energy discharge resulting from the short-circuit. In accordance with this one-dimensional (x-axis) heat conduction model, the thermal energy generated by the short-circuit in the cell 112 is partially conducted through the cell 112 and to the outer surfaces 115, 117 of the cell 112. The close proximity of an adjacent cell 110 to the short-circuited cell 112 permits the thermal energy conducted to the outer surfaces 115, 117 of the cell 112 to dissipate into the adjacent cell 110.
In a similar manner, an adjacent cell 114, having an outer surface 113 in thermal contact with an outer surface 117 of the cell 112, conducts heat produced by the cell 112 through the thermal contact interface 113, 117. In this illustrative example, the adjacent cells 110, 114 include outer surfaces 111, 113 which are in intimate thermal contact with the outer surfaces 115, 117 of the cell
112. It is understood that an insert element, such as a foam or metallic flat spring element, or thermally conductive material, may be situated between adjacent cells. Although not depicted in Fig. 5, it is understood that the heat generated by the short-circuited cell 112 is also conducted in the y and z directions and, in particular, to adjacent and neighboring cells via the thermal conductors and thermally conductive, electrically resistive material as is depicted in Fig. lC.
It is believed that immediately following a short-circuit event in the cell 112, approximately 50% of the generated heat dissipates in the x- direction to adjacent cells 110, 114, while the remaining 50% is dissipated via the thermal conductors and thermally conductive, electrically resistive material. As time progresses, a disproportionate amount of the excess heat is dissipated via the thermal conductor route. It is noted that the end cells of the cell stack require the presence of an adjacently situated heat sink, such as the metal plate 75 shown in Fig. 1C, which is in intimate contact with end cell 74.
Those skilled in the art will appreciate that the energy increase within the short-circuited cell 112, and the rate at which the energy generated from the short-circuit event is dissipated into adjacent cells 110, 114, can be characterized through use of Fourier's Law of Heat Conduction. In describing a process by which heat generated from the short-circuited cell 112 is conducted to adjacent cells 110, 114, a brief discussion of a generalized one-dimensional heat conduction analysis may be useful. It is understood that the following description is provided for purposes of illustration only, and ignores three- dimensional transient heat transfer considerations.
In the energy storage system illustrated in Fig. 5, the rate at which heat flows axially through the short-circuited cell 112 is denoted as Qgen, which represents the heat generated per unit time in the cell 112 of thickness dx. The heat conducted into the volume element 118 at a location x = xo is given by the parameter Qx. The heat conducted out of the volume element 118 at a location x = x + dx is given by the parameter Qx+dX. In this simplistic description, the quantity Qgen represents the heat energy generated throughout the volume element 118 which is dependent on the rate of heat generation per unit volume per unit time, represented by the parameter q, and the volume of the element 118. The resulting energy balance equation is given by: Qx + Qgen - Qx+dx [1 ] and;
- Qgen = qAdx [2]
where, Qx, Qx+dx, and Qgen represent heat flow rates measured in watts (W), q represents the rate of heat generation per unit volume per unit time measured in watts/m3, dx represents the thickness of the volume element 118, and A represents the cross-sectional area of the volume element 118. Those skilled in the art will appreciate that a temperature increase within the energy storage system shown in Fig. 5 due to a short-circuit event can be appropriately managed by understanding the thermal characteristics and energy producing capability of the cells. An in-situ thermal management system in accordance with the principles of the present invention may be employed to dissipate excess thermal energy resulting from a short-circuit event without necessity of an external active thermal management scheme, such as a forced cooling or forced convection apparatus. The in-situ thermal management methodology described herein may be implemented by understanding the heat capacity and heat dissipation characteristics of the particular cells used in an energy storage system, and appropriately limiting the energy content of the cells.
An important consideration that impacts the design of a multiple- cell energy storage system concerns the temperature at which the materials of a particular cell technology break down or degrade such that overall cell performance is significantly reduced. By way of example, a cell having a construction of the type shown in Figs. 1 A-1C and 3 has a breakdown temperature of approximately 180° C, which represents the melting point of lithium. Employment of an in-situ thermal management scheme implemented in accordance with the principles of the present invention prevents the temperature of a cell from reaching a breakdown temperature, or a safety temperature lower than the breakdown temperature, even under short-circuit conditions.
The heat dissipation characteristics of a particular cell are dependent on a number of factors, including the cell's technology, dimensions, and thermal/electrical properties. Taking into consideration these known factors, the heat dissipation characteristics of a cell may be altered and optimized. Since heat dissipation in the cell 112 is a function of thermal contact surface area with respect to contact surfaces of adjacent cells 110, 114, the maximum energy content per unit contact surface area required to maintain the cell temperature below a breakdown or safety temperature may be determined. By way of example, and with reference to Fig. 6, there is shown in graphical form a relationship between the maximum temperature of a cell having a construction as shown in Figs. 1 A-1C and 3 under short-circuit conditions and a ratio of normalized energy content-to-contact surface area for the cell. It is to be understood that the graph of Fig. 6 characterizes a cell having a particular chemistry and having particular geometric and thermal/electrical properties.
Using the graph shown in Fig. 6, the energy content of a cell and the physical dimensions of the cell may be selected so that the ratio of energy content-to-cell surface area is kept within a range such that the maximum cell temperature remains below a breakdown or safety temperature, even under short- circuit conditions. An energy content-to-contact surface area ratio of less than approximately 0.0050 Wh/cm for a thin-film lithium polymer cell will ensure that a worst-case temperature resulting from a short-circuit in the cell does not exceed the melting point of the lithium elements within the cell (i.e., 180° C). If it desired to design the cell to ensure that a maximum short- circuited cell temperature does not exceed a safety temperature, such as 130° C, the energy content and contact surface area of the cell may be appropriately selected using the graph of Fig. 6. It is understood that graphs similar to that shown in Fig. 6 which characterize maximum cell temperature under short- circuit conditions relative to the ratio of energy content-to-contact surface area may be developed for energy storage cells constructed using technologies other than those described herein. It is noted that Fig. 18, for example, depicts a relationship between energy content and maximum cell temperature for a cell having a similar construction as that shown in Figs. 1A-1C and 3 but a different cathode oxide.
The depictions of energy storage cells shown in Figs. 7-9 are provided to illustrate that an in-situ thermal management design approach may be employed for energy storage cells having varying configurations. For example, the length (L), height (H), width (w), or radius (r) may be varied as needed for a given application, with the constraint that the ratio of energy content-to-contact surface area remain in a range that prevents the worst-case cell temperature from exceeding the cell breakdown temperature.
In order to facilitate the proper design and manufacture of thermally stable energy storing modules and devices which contain a number of closely situated electrochemical cells of a given technology, it is useful to express the maximum temperature achievable by the cells under worst-case conditions (i.e., a short-circuit) as a function of several variables, including the ratio of energy content of the cell to cell volume, conductivity of the cells, thermal conductance, and cell thickness. The following equations characterize the maximum temperature, (Tmax), of a short-circuited cell of a given technology when the cell is packaged in an energy storing module such as that depicted in Figs. 4, 10, and 14. It is noted that the equations below were developed by use of numerical simulations of a multiple-cell module at an initial operating temperature of 60° C. It is further noted that these equations were developed based on a cell technology implicated in Fig. 18. Using the following equations, it is possible to calculate the conductance of a thermal conductor required to safely dissipate excess heat generated by a short-circuited cell.
Equation [3] below mathematically characterizes the maximum cell temperature of a thin-filmed electrochemical cell, which does not include a foam core element, as a function of various operative parameters. The dimensions of the cell characterized in Equation [3] are given as 0.135m x 0.149m x 0.054m. The maximum cell temperature for the cell is given by:
Tmax = 1/1.1-1/1.2.0.037738.(l/(PcelI.Cpcell))° 385s -(Q/kcell) • (δ)06146 • (K/L)"0077 [3]
where, Tmax represents the maximum temperature reached by a short-circuited cell in a module (° C), pceιι represents the density of the cell (kg/m3), Cpceπ represents the heat capacity of the cell (J/kgK), Q represents the energy content of one cell per unit volume (Wh/m ), kcell represents the conductivity of the cell in the cell-to-cell axial direction (W/mK), δ represents cell thickness in the cell- to-cell axial direction (mm), and K L represents the conductance of the thermal conductor (W/m2K).
Using Equation [3] above, a relationship between maximum temperature of a short-circuited cell as a function of the cell's energy content for a given cell chemistry and configuration may be developed. A relationship between maximum cell temperature as a function of cell thickness may also be developed. By way of example, and with reference to Figs. 18-19, there is depicted a relationship between maximum cell temperature as a function of energy content and cell thickness, respectively. The data reflected in Figs. 18-19 was developed with the following variables held constant: kcell = 0.4 W/mK, K/L = 400 W/m2K, Pceιι • Cpce„ = 1218 • 1435 J/m3K.
It can be seen from Fig. 18 that a thin-film electrochemical cell of the type characterized above should have an energy content which is limited to less than approximately 38 Wh to ensure that the maximum temperature of the cell will not exceed a breakdown temperature, such as the melting point of lithium (i.e., 180° C). It is interesting to note the linearity of the maximum cell temperature-to-energy content relationship depicted in Figs. 18 and 6, given the difference in cell technology. It can be seen from Fig. 19 that the thickness of the cell should not exceed approximately 8.5 mm in order to ensure that the maximum temperature of the cell does not exceed the 180° C breakdown temperature.
Equation [4] below characterizes maximum cell temperature for an energy storing module of the same cell technology as that implicated in Equation [3] in which some of the cells include a foam core element compressed to approximately 2 mm. More specifically, Equation [4] characterizes maximum cell temperature for a module design in which compressed foam core elements are provided in every two electrochemical cells. In this case, maximum cell temperature for such a module configuration is given by:
= 0.037738 • (l/(pCeiι Cpceιι)f 0.3 J8δ 5 D60 • • (-δSΛ)Oυ.60114460 • (τKr/L x)-"0υ.0υ7
Figure imgf000016_0001
/7/ [4] It is interesting to note that Equations [3] and [4] differ only by constants (i.e., the constants 1/1.1 and 1/1.2 in Equation [3]).
Equation [5] characterizes the maximum cell temperature for a module having cells of the same technology implicated in Equations [3]-[4], wherein the cells incorporate a foam core element that is thinner than the element associated with Equation [4] above. More specifically, Equation [5] below assumes that a foam core element having a thickness of approximately 1/32 inches is provided in every two cells of the cell stack. The foam core element is fabricated from Poron S2000. The maximum cell temperature for a module having this configuration is given by:
Tmax = 1/1.1 . 0.037738 • (l/(Pce„ • Cpcel,)) 3856 • (Q/kcell) • (δ)06146 • (K/L)"0077 [5]
It is noted that the term pceιι • Cpceιι allows Equations [3]-[5] to be used to quantify the effect of heat capacity of the components within the cell on the maximum cell temperature, Tmax, reached during a short-circuit event. These equations, therefore, may be used to characterize maximum cell temperatures under similar situations for energy storing cells of differing technologies.
These equations may also be employed to characterize the effects of modifications and improvements in cell design and construction. It is noted that the numerical simulations used to develop Equations [3]-[5] were directed to the investigation of electrochemical cells having an energy content that varied from approximately 30 to 40 Wh, a cell thickness, δ, that varies from approximately 5.4 and 7.8 mm, and cells that utilize a thermal conductor having a conductance value, K/L, that varies between approximately 200 and 600
W/m2K.
The in-situ thermal management approach described above with reference to Figs. 1C and 5 is generally applicable for managing short-circuit temperature increases occurring in a single cell of a grouping of cells. In applications in which a significant number of parallel connected cells are configured in a stack or bundle, an enhanced in-situ short-circuit protection scheme may be implemented to prevent thermal runaway within the cell stack, and to isolate a particular cell from the parallel connection upon occurrence of a short-circuit in the cell.
In the embodiment of an energy storage system illustrate in Fig. 10, the energy storage device 120 includes eight energy storage cells respectively connected in parallel to common positive and negative terminals
124, 125. The cell EC1 is shown as a short-circuit. Given this arrangement, and with reference to Fig. 11, it can be seen that only one short-circuited cell within a stack of eight cells can be managed using the above-described in-situ thermal management methodology without exceeding the breakdown temperature of the cell material. An in-situ short-circuit protection device may be incorporated into an energy storage system to prevent multiple short-circuit events from occurring. In accordance with one embodiment of the present invention, and as shown in Fig. 10, a fuse 123 is connected in series with a respective cell 122 within the multiple-cell energy storage device 120. In the event that a short- circuit occurs in any of the parallel connected cells 122, the fuse 123 of the defective cell 122 blows so as to electrically isolate the short-circuited cell 122 from the parallel connection. The heat generated during development of the short-circuit in the cell 122 and after blowing of the fuse 123 is conducted to cells adjacent the defective cell 122 in a manner previously described. As such, the maximum temperature attainable by a cell under worst-case conditions is well below the breakdown temperature of the cell. More particularly, the data of Fig. 11 confirms that the temperature of a short-circuited cell within the cell stack never exceeds a safety temperature of 130° C when an in-situ short-circuit protection device is employed. Referring now to Fig. 12, there is illustrated a graph which characterizes the effect on cell current upon the occurrence of a short-circuit in a thin-film electrochemical cell. A thin-film cell of the type shown in Figs. 1A-1C and 3, as well as other types of high-energy cells, exhibit a significant short-term increase in cell current due to the capacitive characteristics of the cell. For example, the current in the cell characterized in Fig. 12 spikes at a value in excess of 500 A in less than approximately 100 milliseconds. Following the current spike, the current in the cell rapidly decays to approximately 150 A after 1 second, and gradually decays thereafter. At 5 seconds following the short- circuit event, the cell current reaches a value of approximately 60 A.
The characteristic current spike that occurs immediately after a short-circuit event in a high-energy cell is advantageously exploited by an in-situ short-circuit protection device implemented in accordance with the principles of the present invention. In the embodiment shown in Fig. 10, for example, each of the fuses 123 connected in series with a corresponding energy storage cell 122 are designed to activate in response to a current spike generated from a short- circuit in the cell 122. A fuse 123 typically has a current rating that prevents the fuse from activating during normal operation, yet permits the fuse to activate in response to a short-circuit condition. Exploiting the current spike as a triggering mechanism for the fuse 123 provides for a large current gap between the maximum operating current level of the cell 122 and the minimum activation current level of the fuse 123. In accordance with one embodiment, the parallel connected cells of an energy storage device have a structure and behavior similar to those previously described with reference to Figs. 1A-1C and 3. In such a configuration, the fuses connected in series with the cells have a current rating of approximately 50 A. By utilizing the capacitive effect of the cell to trigger the 50 A fuse, unintentional activation of the fuse is avoided, providing for both safe and reliable short-circuit protection of the energy storage device.
In some applications, protection against accidental shorting of an energy storage device or cell, such as through a foreign conductive implement or material, may be of primary concern. It may be desirable, therefore, to employ a fuse that is activated more slowly than the fast acting fuse described above. For example, a fuse that activates after several hundred milliseconds or several seconds after occurrence of a short-circuit in the cell may be employed. Although excess heat is generated between the time the short occurs and the time the fuse blows, the in-situ thermal management methodology described previously provides for the safe dissipation of such excess heat.
In Fig. 13, there is illustrated an embodiment of a short-circuit protection device fabricated in an integrated package. The integrated device 130 includes an enclosure 132 within which eight fuses (not shown) are mounted. A first contact of each fuse is connected in series with a corresponding one of eight terminals 134, and a second contact of the each fuse is connected to a common bus 140. Each of the terminals 134 includes a lead 136 and a contact 138. When the short-circuit protection device 130 is connected to an array of cells, each of the contacts 138 engages a corresponding contact of one of eight cells in the array. The common bus 140 is typically coupled to one or more common busses of other short-circuit protection devices 130 connected to corresponding cell arrays to form a series connected energy storage device, such as a module. In one embodiment, the enclosure 132 has a height, HE, of 16.00 mm, a width, WE, of 7.49 mm, and a length, LE, of 50.80 mm. The lead portion 136 of the terminal 134 has a height, HL, of 12.70 mm, a width, WL, of 1.27 mm, and a length, LL, of 5.00 mm. The contact portion 138 of the terminal 134 has a height, He, and a width, Wc, of 1.27 mm, and a length, Lc, of 13.03 mm. The common bus 140 has a height, HCB, of 6.35 mm, a width, WCB, of 1.27 mm, and a length, LCB, of 49.02 mm.
In Fig.14, there is shown an exploded view of an embodiment of an energy storing module 142 which houses a number of electrochemical cells 144, interconnection hardware, and control hardware and software. In accordance with one embodiment, the module 142 includes a stack of 48 electrochemical cells 144 which are interconnected through use of a interconnect board 147. Short-circuit protection circuitry, such as an integrated short-circuit protection pack 148, is typically provided on the interconnect board 147. Each of the six integrated short-circuit protection packs 148 disposed on the interconnect board 147 electrically couple to a corresponding one of six cell packs 143 upon mounting the interconnect board 147 in place above the stack of cells 144.
The volume of an electrochemical cell of the type described previously with regard to Fig. 1 varies during charge and discharge cycling due to the migration of lithium ions into and out of the lattice structure of the cathode material. This migration creates a corresponding increase and decrease in total cell volume on the order of approximately five to six percent during charging and discharging, respectively. In order to accommodate variations in cell volume resulting from charge and discharge cycling of a grouping of cells, a pressure producing apparatus is employed to maintain the cells in a continuous state of compression to ensure continuous intimate contact between cell of the cell stack. It is considered desirable that the compressive forces, whether produced internally or externally of the cell, be distributed fairly uniformly over the surface of application.
The stack of electrochemical cells 144 shown in Fig. 14 are banded together by use of two bands 146 and two opposing thrust plates 145. The 48 electrochemical cells 144 are subjected to continuous compressive forces generated by use of the bands 146/thrust plates 145 and a foam or spring-type element disposed in each of the cells 144 and/or between all or selected ones of the cells 144. It is noted that the foam or spring-type core element provided in the center of each of the cells 144 serves to distribute pressure evenly between the cells 144, which is of particular importance as cell volumes change during charge and discharge cycling.
In the embodiment illustrated in Fig. 15, a metal strap 194 includes a wave-like spring 198 which generates tension forces that cause the thrust plates 194, in turn, to exert compressive forces on the cell stack 192. It is understood that the tension spring apparatus illustrated in Fig. 15 may be implemented using a number of coil springs or using elastomeric material, and that a combination of metallic and elastomeric spring materials may also be advantageously employed. Further, it will be appreciated that foam or other spring elements may be incorporated within the cell stack and/or within individual cells in combination with a tension spring apparatus external to cell stack.
Figure 16 illustrates an embodiment of a strap apparatus 180 which is particularly useful in constraining a number of electrochemical cells configured as a stack or bundle. In contrast to a strap apparatus which is substantially non-extendible in its length, the strap apparatus shown in Fig. 16 incorporates a unique clamp 182 which significantly enhances the efficacy of a cell stack pressure system. The strap apparatus includes two bands 180 each having C-shaped ends 181. A clamp 182 is attached to a band 180 by coupling the C-shaped ends 181 of the band 180 with corresponding C-shaped ends 184 of the clamp 182. It is assumed that the bands 180 are disposed around the stack of cells in a manner as shown in Fig. 15. The clamp 182 includes a hinge 186 integral to the clamp 182 which is collapsible onto a contact surface 188 of the clamp 182 when subjected to sufficient force.
When the hinge 186 is collapsed onto the contact surface 188, the
C-shaped ends 184 of the clamp 182 are pulled towards each other which, in turn, produces a tension force in the C-shaped ends of the bands 180. The magnitude of the tension force induced in the bands 180 by actuation of the clamps 182 is moderated by a sign wave-shaped spring 189 integral to the clamps 182. The sign wave-shaped spring 189 may be configured, in terms of shape, thickness, and material, to provide for a desired amount of expansion and retraction of the strap apparatus during charge/discharge cycling of the cells. It will, of course, be understood that modifications and additions can be made to the various embodiments discussed hereinabove without departing from the scope or spirit of the present invention. By way of example, a short-circuit protection device may include thermally activated fuses, such as Model NTE8090 manufactured by NTE Electronics, rather those described herein. Thermally activated fuses typically activate at a prescribed temperature, such as a temperature below a breakdown temperature. Also, a thermally activated fuse may be connected in series with a current activated fuse which provides for increased activation reliability. Further, the principles of the present invention may be employed for use with battery technologies other than those exploiting lithium polymer electrolytes, such as those employing nickel metal hydride (Ni-MH), lithium-ion, (Li-Ion), and other high energy battery technologies. Accordingly, the scope of the present invention should not be limited by the particular embodiments discussed above, but should be defined only by the claims set forth below and equivalents thereof.

Claims

CLAIMSWhat we claim is:
1. An in-situ thermal management system for an energy storing unit, comprising: a plurality of thin-film electrochemical cells each being coupled in parallel to common positive and negative connections, each of the electrochemical cells having a ratio of energy content-to-contact surface area such that thermal energy produced by a short-circuit in a particular cell of the plurality of cells is conducted to a cell adjacent the particular cell so as to prevent a temperature of the particular cell from exceeding a breakdown temperature; and a plurality of fuses each coupled in series with one of the electrochemical cells, a fuse coupled to the particular cell being activated by a current spike capacitively produced by the particular cell upon occurrence of the short-circuit in the particular cell, thereby electrically isolating the particular cell from the common positive and negative connections.
2. The system of claim 1, wherein the fuses are activated by a current spike having an amperage ranging between approximately 300 A and 600 A.
3. The system of claim 1, wherein the fuses have a current rating of approximately 50 A.
4. The system of claim 1, wherein the fuses are fabricated as an integrated package.
5. The system of claim 1, wherein the breakdown temperature represents a melting temperature of the particular cell.
6. The system of claim 1 , wherein the ratio of energy content-to- contact surface area is less than approximately 0.006 Wh/cm2.
7. The system of claim 1, wherein each of the plurality of electrochemical cells has a prismatic configuration.
8. The system of claim 1, wherein each of the plurality of electrochemical cells has a surface area ranging between approximately 100 cm2 and 400 cm2 and an energy content ranging between approximately 10 Wh and 40 Wh.
9. An in-situ thermal management system for an energy storing unit, comprising: a plurality of energy storing cells connected in parallel to common positive and negative connections and maintained in a state of compression; and a plurality of short-circuit protection devices each being coupled in series to one of the plurality of energy storing cells, a particular short-circuit protection device of the plurality of short-circuit protection devices coupled to a particular cell of the plurality of cells being activated by a current spike capacitively produced upon occurrence of a short-circuit in the particular cell, the particular cell being electrically isolated from the common positive and negative connections upon activation of the particular short-circuit device.
10. An in-situ thermal management system for an energy storing unit, comprising: a plurality of substantially planar thin-film electrochemical cells each having a breakdown temperature; the plurality of electrochemical cells being arranged such that a planar surface of a particular cell of the plurality of cells is in thermal contact with a planar surface of a cell disposed adjacent the particular cell; and the planar surfaces of the particular cell and the adjacent cell each having a ratio of energy content-to-contact surface area such that thermal energy produced by a short-circuit condition arising in the particular cell is conducted to the adjacent cell so as to prevent a temperature of the particular cell from exceeding the breakdown temperature.
11. The system of claim 10, wherein each of the plurality of electrochemical cells comprises lithium, and the breakdown temperature represents a melting temperature of lithium.
12. The system of claim 10, wherein the planar surfaces of the particular and adjacent cell each have a ratio of energy content-to-contact surface area such that thermal energy produced by the short-circuit condition occurring in the particular cell is conducted to the adjacent cell so as to prevent a temperature of the particular cell from exceeding a safety temperature, the safety temperature being lower than the breakdown temperature.
13. The system of claim 12, wherein the safety temperature is \30 J Celsius.
14. The system of claim 10, wherein the ratio of energy content-to- surface area is less than approximately 0.006 Wh/cm2.
15. The system of claim 10, wherein the ratio of energy content-to- surface area ranges between approximately 0.0034 Wh/cm2 and 0.0038 Wh/cm2.
16. The system of claim 10, wherein each of the plurality of electrochemical cells has a prismatic configuration.
17. The system of claim 10, wherein each of the plurality of electrochemical cells has a surface area ranging between approximately 100 cm2 and 400 cm2.
18. The system of claim 10, wherein each of the plurality of electrochemical cells has an energy content ranging between approximately 10 Wh and 40 Wh.
19. The system of claim 10, wherein each of the plurality of electrochemical cells has a thickness that varies between approximately 3 mm to 10 mm and the ratio of energy content-to-contact surface area is less than approximately 0.006 Wh/cm .
20. A method of providing short-circuit protection for a plurality of parallel connected energy storing cells, comprising: maintaining the energy storing cells in thermal contact with one another; generating current using the energy storing cells; electrically isolating a short-circuited cell of the plurality of cells in response to a current spike produced by the short-circuited cell; and conducting heat generated by the short-circuited cell to other ones of the plurality of energy storing cells so that a temperature of the short-circuited cell remains below a breakdown temperature.
21. The method of claim 20, wherein electrically isolating the short- circuited cell comprises blowing a fuse connected in series with the short- circuited cell.
22. The method of claim 21 , wherein the fuse is blown in less than 100 milliseconds.
23. The method of claim 20, wherein the current spike produced by the short-circuited cell has an amperage in the range of approximately 300 A to 600 A.
24. The system of claim 1 , wherein each of the plurality of fuses comprises a thermal fuse.
25. An in-situ thermal management system for an energy storing unit, comprising: a plurality of thin-film electrochemical cells each having substantially planar opposing surfaces and an associated critical temperature over which non-nomimal cell behavior occurs, the cells arranged such that a respective planar surface of adjacent cells are in thermal contact; and a thermal conductor connected to each of the cells; wherein a maximum temperature, Tmax, of a short-circuited cell of the plurality of cells is generally characterized by the equation:
Tmax = W ΓÇó (l/(pcdl ΓÇó CPcell))X ΓÇó (Q c╬▓ll) ΓÇó (╬┤)> ΓÇó (K/L) "" where, Tmax represents the maximum temperature of the short- circuited cell (┬░C), pceii represents a density of the short-circuited cell (kg/m3), CpCei╬╣ represents a heat capacity of the short-circuited cell (J/kgK), Q represents an energy content of the short-circuited cell per unit volume (Wh/m ), kcell represents a conductivity of the short-circuited cell in the cell-to-cell axial direction (W/mK), ╬┤ represents a thickness of the short-circuited cell in a cell-to- cell axial direction (mm), K/L represents a conductance of the thermal conductor (W/m2K), and variables w, x, y, and z represent constants that are selected for a cell having a selected configuration so as to prevent the maximum temperature, Tmax, of the short-circuited cell from exceeding the critical temperature.
26. The system of claim 25, wherein the thickness, ╬┤, of the short- circuited cell is less than approximately 8.5 mm.
27. The system of claim 25, wherein the energy content of the cells is less than approximately 40 Wh.
28. The system of claim 25, wherein the variables x, y, and z are selected so that the maximum temperature, Tmaχ, of the short-circuited cell is linearly related to an energy content of the short-circuited cell.
29. The system of claim 25, wherein the variables x, y, and z are selected so that the maximum temperature, Tmaχ, of the short-circuited cell is linearly related to the thickness, δ, of the short-circuited cell.
30. The system of claim 25, wherein the variable w varies as a function of the presence and thickness of a foam core element incorporated within at least some of the plurality of cells.
PCT/US1998/015299 1997-07-25 1998-07-23 In situ short-circuit protection system and method for high-energy electrochemical cells WO1999005747A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP19980935973 EP1021850A1 (en) 1997-07-25 1998-07-23 In situ short-circuit protection system and method for high-energy electrochemical cells
JP2000504628A JP4267812B2 (en) 1997-07-25 1998-07-23 Field short circuit protection system and method for high energy electrochemical cells
CA 2297839 CA2297839C (en) 1997-07-25 1998-07-23 In situ short-circuit protection system and method for high-energy electrochemical cells
AU85109/98A AU8510998A (en) 1997-07-25 1998-07-23 In situ short-circuit protection system and method for high-energy electro chemical cells

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/900,929 US6099986A (en) 1997-07-25 1997-07-25 In-situ short circuit protection system and method for high-energy electrochemical cells
US08/900,929 1997-07-25

Publications (1)

Publication Number Publication Date
WO1999005747A1 true WO1999005747A1 (en) 1999-02-04

Family

ID=25413313

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1998/015299 WO1999005747A1 (en) 1997-07-25 1998-07-23 In situ short-circuit protection system and method for high-energy electrochemical cells

Country Status (6)

Country Link
US (2) US6099986A (en)
EP (1) EP1021850A1 (en)
JP (1) JP4267812B2 (en)
AU (1) AU8510998A (en)
CA (1) CA2297839C (en)
WO (1) WO1999005747A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6548206B1 (en) * 1997-07-25 2003-04-15 3M Innovative Properties Company In-situ short-circuit protection system and method for high-energy electrochemical cells
WO2007028803A1 (en) * 2005-09-06 2007-03-15 Dilo Trading Ag Special purpose lithium polymer batteries special purpose arrangements and method for prodcution thereof
WO2010037798A2 (en) * 2008-09-30 2010-04-08 Magna Steyr Fahrzeugtechnik Ag & Co Kg Energy accumulator module

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6902847B1 (en) * 1998-05-20 2005-06-07 Osaka Gas Company Limited Non-aqueous secondary cell and method for controlling the same
JP3497380B2 (en) * 1998-06-02 2004-02-16 日本碍子株式会社 Lithium secondary battery
US6291972B1 (en) * 1999-02-17 2001-09-18 Chaojiong Zhang System for battery formation, charging, discharging, and equalization
US6821671B2 (en) * 2002-03-01 2004-11-23 Lg Chem, Ltd. Method and apparatus for cooling and positioning prismatic battery cells
KR100880388B1 (en) * 2005-04-20 2009-01-23 주식회사 엘지화학 Housing Member For Battery Module
KR101029021B1 (en) * 2005-12-02 2011-04-14 주식회사 엘지화학 Battery Module of High Cooling Efficiency
US8628872B2 (en) * 2008-01-18 2014-01-14 Lg Chem, Ltd. Battery cell assembly and method for assembling the battery cell assembly
JP2009199825A (en) * 2008-02-20 2009-09-03 Sumitomo Chemical Co Ltd Device with electrode group
US8486552B2 (en) * 2008-06-30 2013-07-16 Lg Chem, Ltd. Battery module having cooling manifold with ported screws and method for cooling the battery module
US8426050B2 (en) * 2008-06-30 2013-04-23 Lg Chem, Ltd. Battery module having cooling manifold and method for cooling battery module
US7883793B2 (en) * 2008-06-30 2011-02-08 Lg Chem, Ltd. Battery module having battery cell assemblies with alignment-coupling features
US8153290B2 (en) * 2008-10-28 2012-04-10 Tesla Motors, Inc. Heat dissipation for large battery packs
US8815429B2 (en) 2009-01-12 2014-08-26 A123 Systems Llc Busbar supports and methods of their use for battery systems
US9337456B2 (en) * 2009-04-20 2016-05-10 Lg Chem, Ltd. Frame member, frame assembly and battery cell assembly made therefrom and methods of making the same
US8663829B2 (en) * 2009-04-30 2014-03-04 Lg Chem, Ltd. Battery systems, battery modules, and method for cooling a battery module
US8663828B2 (en) * 2009-04-30 2014-03-04 Lg Chem, Ltd. Battery systems, battery module, and method for cooling the battery module
US8852778B2 (en) * 2009-04-30 2014-10-07 Lg Chem, Ltd. Battery systems, battery modules, and method for cooling a battery module
CN202978302U (en) 2009-12-04 2013-06-05 A123系统公司 Cell system with integrated power supply management system and telescopic cell breaker assembly
US9147916B2 (en) 2010-04-17 2015-09-29 Lg Chem, Ltd. Battery cell assemblies
JPWO2011151981A1 (en) 2010-06-02 2013-07-25 パナソニック株式会社 Battery module
JP5972872B2 (en) * 2010-07-22 2016-08-17 バシウム・カナダ・インコーポレーテッド Current collector terminal for electrochemical cell
US8133608B2 (en) 2010-08-04 2012-03-13 Tesla Motors, Inc. Battery pack with cell-level fusing
US8932739B2 (en) 2010-08-04 2015-01-13 Tesla Motors, Inc. Battery pack configuration to reduce hazards associated with internal short circuits
US8133287B2 (en) * 2010-08-04 2012-03-13 Tesla Motors, Inc. Method of controlled cell-level fusing within a battery pack
US8469404B2 (en) 2010-08-23 2013-06-25 Lg Chem, Ltd. Connecting assembly
US8920956B2 (en) 2010-08-23 2014-12-30 Lg Chem, Ltd. Battery system and manifold assembly having a manifold member and a connecting fitting
US8353315B2 (en) 2010-08-23 2013-01-15 Lg Chem, Ltd. End cap
US8758922B2 (en) 2010-08-23 2014-06-24 Lg Chem, Ltd. Battery system and manifold assembly with two manifold members removably coupled together
US9005799B2 (en) 2010-08-25 2015-04-14 Lg Chem, Ltd. Battery module and methods for bonding cell terminals of battery cells together
US8662153B2 (en) 2010-10-04 2014-03-04 Lg Chem, Ltd. Battery cell assembly, heat exchanger, and method for manufacturing the heat exchanger
US9065096B2 (en) * 2011-02-24 2015-06-23 Samsung Sdi Co., Ltd. Fuel cell stack
JP2012182890A (en) * 2011-02-28 2012-09-20 Sharp Corp Protective device for secondary battery, secondary battery device, and secondary battery
US8649140B2 (en) 2011-03-04 2014-02-11 Electrochem Solutions, Inc. Voltage activated 2nd level safety circuit for permanent isolation
US8288031B1 (en) 2011-03-28 2012-10-16 Lg Chem, Ltd. Battery disconnect unit and method of assembling the battery disconnect unit
US9178192B2 (en) 2011-05-13 2015-11-03 Lg Chem, Ltd. Battery module and method for manufacturing the battery module
US9496544B2 (en) 2011-07-28 2016-11-15 Lg Chem. Ltd. Battery modules having interconnect members with vibration dampening portions
TWI462373B (en) * 2012-06-28 2014-11-21 Energy Control Ltd Secure battery pack formed by a plurality of secondary batteries
GB2504116A (en) * 2012-07-19 2014-01-22 Energy Control Ltd Secondary Battery Pack
TWI449244B (en) * 2012-08-22 2014-08-11 Energy Control Ltd Battery pack formed by connecting two secondary batteries with two fuses in parallel
US9287726B2 (en) * 2013-11-06 2016-03-15 The Boeing Company Virtual cell for battery thermal management
CN104466068B (en) * 2014-10-27 2017-02-15 深圳市快车道新能源发展有限公司 Method for connecting storage battery combined system
JP6288057B2 (en) * 2015-12-02 2018-03-07 トヨタ自動車株式会社 Stacked all-solid battery
US9991699B2 (en) 2016-05-02 2018-06-05 Microsoft Technology Licensing, Llc Enablement of device power-on with proper assembly
JP7056142B2 (en) * 2017-12-25 2022-04-19 トヨタ自動車株式会社 Battery module
JP7215270B2 (en) 2019-03-22 2023-01-31 トヨタ自動車株式会社 Case manufacturing method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4383013A (en) * 1980-07-23 1983-05-10 Chloride Silent Power Limited High temperature multicell electrochemical storage batteries
JPS5991658A (en) * 1982-11-18 1984-05-26 Japan Storage Battery Co Ltd Monoblock container for alkaline storage battery
US4973936A (en) * 1989-04-27 1990-11-27 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Adminstration Thermal switch disc for short circuit protection of batteries
JPH0917416A (en) * 1995-06-30 1997-01-17 Fuji Elelctrochem Co Ltd Battery having explosion-proof function

Family Cites Families (165)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2899635A (en) * 1952-03-07 1959-08-11 Electric battery with charge testing means
US3390014A (en) * 1960-05-11 1968-06-25 Eisler Paul Secondary electric batteries having plurality of thin flexible intermediate bipolar plates
US3193412A (en) * 1962-02-20 1965-07-06 Electric Storage Battery Co Electric battery
FR1586636A (en) * 1968-02-29 1970-02-27
US3630783A (en) * 1970-05-11 1971-12-28 Mallory Battery Canada Heat-shrinkable packaging for batteries
JPS5218891B1 (en) * 1971-03-19 1977-05-25
FR2193242B1 (en) * 1972-07-13 1977-05-13 Siemens Ag
FI49090C (en) * 1972-11-10 1975-03-10 Pentti Juuse Tamminen Galvanic stacking battery.
US3793501A (en) * 1972-12-04 1974-02-19 Ici America Inc Explosive switch
US3899355A (en) * 1974-02-14 1975-08-12 Polaroid Corp Battery assembly
US4152825A (en) * 1974-06-10 1979-05-08 Polaroid Corporation Method of making a flat battery
US4105815A (en) * 1974-08-08 1978-08-08 Polaroid Corporation Flat battery with electrodes in slurry form
US4028479A (en) * 1974-12-26 1977-06-07 Polaroid Corporation Flat battery
US3937635A (en) * 1975-01-09 1976-02-10 Wilson Greatbatch Lithium-iodine battery
US4105807A (en) * 1975-07-28 1978-08-08 Unican Electrochemical Products Ltd. Production of thin, stable, solid electrolyte films of high ionic conductivity
US4060669A (en) * 1975-09-10 1977-11-29 Polaroid Corporation Flat battery
ES450123A1 (en) 1976-07-24 1977-12-16 Celaya Emparaza Y Galdos S A Electric batteries
US4098965A (en) * 1977-01-24 1978-07-04 Polaroid Corporation Flat batteries and method of making the same
US4150266A (en) * 1977-01-27 1979-04-17 Networks Electronic Corp. Miniature pyrotechnic squib switch, single pole, normally open
US4091186A (en) * 1977-11-07 1978-05-23 Esb Incorporated Dry cell battery having electrical spring contact adhered to terminal
US4207389A (en) * 1977-11-25 1980-06-10 P. R. Mallory & Co. Inc. Solid state cells
US4209479A (en) * 1977-11-25 1980-06-24 P. R. Mallory & Co. Inc. Means for improving manufacture of solid state cells
US4303877A (en) * 1978-05-05 1981-12-01 Brown, Boveri & Cie Aktiengesellschaft Circuit for protecting storage cells
US4322484A (en) * 1978-09-05 1982-03-30 General Electric Company Spiral wound electrochemical cell having high capacity
NL7809298A (en) * 1978-09-13 1980-03-17 Electrochem Energieconversie METHOD FOR MANUFACTURING AN ELECTROCHEMICAL CELL OR BATTERY.
DE2849326A1 (en) * 1978-11-14 1980-05-29 Deutsche Automobilgesellsch DISASSEMBLABLE, GAS-TIGHT AND PRESSURE-RESISTANT ELECTRICITY
US4238721A (en) * 1979-02-06 1980-12-09 The United States Of America As Represented By The United States Department Of Energy System and method for charging electrochemical cells in series
US4342978A (en) * 1979-03-19 1982-08-03 S&C Electric Company Explosively-actuated switch and current limiting, high voltage fuse using same
DE3011643A1 (en) * 1980-03-26 1981-10-01 Metallgesellschaft Ag, 6000 Frankfurt ELECTROLYSIS CELL
US4490707A (en) * 1980-08-18 1984-12-25 S&C Electric Company Explosively-actuated, multi-gap high voltage switch
JPS5743526A (en) * 1980-08-27 1982-03-11 Seiko Instr & Electronics Charge control circuit
US4370531A (en) * 1980-09-19 1983-01-25 S&C Electric Company Electric switch and improved device using same
FI65688C (en) * 1981-04-27 1984-06-11 Sporax Oy CONTACT CONTROL FOR BATTERIES I ETT GALVANISKT BATTERI
FR2511547B1 (en) 1981-08-13 1985-08-09 Moli Energy Ltd METHOD FOR INCREASING THE REVERSIBILITY OF AN ELECTRIC BATTERY, ELECTRODE DEVICE FOR CARRYING OUT SAID METHOD AND BATTERY THUS OBTAINED
US4664993A (en) * 1981-08-24 1987-05-12 Polaroid Corporation Laminar batteries and methods of making the same
US4436792A (en) * 1981-11-12 1984-03-13 Nippon Kogaku K.K. Container device for planar battery
US4429026A (en) * 1982-01-20 1984-01-31 Polaroid Corporation Laminar multicell lithium batteries
US4961043A (en) * 1988-03-15 1990-10-02 Norand Corporation Battery conditioning system having communication with battery parameter memory means in conjunction with battery conditioning
CA1173900A (en) * 1982-06-30 1984-09-04 Hydro-Quebec Composite and flexible anodes for non aqueous lithium cells
US4571468A (en) * 1982-07-16 1986-02-18 University Of Texas System Inductive store opening switch
US4479083B1 (en) * 1982-09-30 1998-09-01 Vanner Weldon Inc DC power system having battery voltage equalizer circuit
JPS5973864A (en) * 1982-10-20 1984-04-26 Showa Denko Kk Layer-built sheet-like polymer secondary battery
DE3246968C2 (en) 1982-12-18 1986-03-20 Varta Batterie Ag, 3000 Hannover Electric battery with several cells lying next to one another and arranged parallel to one another
US4923582A (en) * 1982-12-27 1990-05-08 Eltech Systems Corporation Monopolar, bipolar and/or hybrid memberane cell
US4495259A (en) * 1983-02-11 1985-01-22 The Gates Rubber Company Vibration resistant battery
US4758483A (en) * 1983-03-11 1988-07-19 Societe Nationale Elf Aquitaine Novel macromolecular material for use in realizing electrolytes and/or electrodes
US4707795A (en) * 1983-03-14 1987-11-17 Alber Engineering, Inc. Battery testing and monitoring system
US4507857A (en) * 1983-06-22 1985-04-02 Battery Engineering Inc. Electrochemical cell
US4477545A (en) * 1983-06-29 1984-10-16 Union Carbide Corporation Isostatic compression method for producing solid state electrochemical cells
US4654278A (en) * 1983-09-29 1987-03-31 The United States Of America As Represented By The Secretary Of The Navy Thermal cell non-deflagration design
US4525439A (en) * 1983-10-07 1985-06-25 Simonton Robert D Connector aperture seal for a galvanic cell
DE3426199C2 (en) 1984-07-17 1994-02-03 Asea Brown Boveri Bridging element
US4547438A (en) * 1984-12-18 1985-10-15 Duracell Inc. Battery assembly
US4670703A (en) * 1985-05-06 1987-06-02 General Electric Company Battery charger with three different charging rates
US4692577A (en) * 1985-10-25 1987-09-08 S&C Electric Company Switch for a high-voltage interrupting module
US4713597A (en) 1985-12-04 1987-12-15 Powerplex Technologies, Inc. Silicon diode looping element for protecting a battery cell
US4691085A (en) * 1985-12-19 1987-09-01 S&C Electric Company High voltage interrupting switch with improved contact connection arrangement and method
IL78893A (en) * 1986-05-23 1991-08-16 Univ Ramot Electrochemical battery packaging
FR2606216A1 (en) * 1986-10-30 1988-05-06 Elf Aquitaine ION CONDUCTION MATERIAL
CA1288473C (en) * 1987-03-11 1991-09-03 Andre Belanger Thin electrode carried on electronically conducting strip, and process for itsmanufacture
US4927717A (en) * 1987-06-01 1990-05-22 Eltech Systems Corporation Bipolar metal/air battery
US4828939A (en) * 1987-06-01 1989-05-09 Eltech Systems Corporation Bipolar metal/air battery
US4752540A (en) * 1987-06-05 1988-06-21 Honeywell Inc. Polymeric enclosures for non-aqueous active metal cells
FR2616971A1 (en) * 1987-06-18 1988-12-23 Elf Aquitaine INTERMEDIATE ASSEMBLY FOR THE PRODUCTION IN THE FORM OF THIN FILMS OF A LITHIUM BATTERY, METHOD OF MAKING SAME, AND METHOD FOR PRODUCING THE ACCUMULATOR
GB8715708D0 (en) 1987-07-03 1987-08-12 Chloride Silent Power Ltd Batteries
US4816354A (en) * 1988-03-09 1989-03-28 Tamminen Pentti J Alkaline cell battery and method for manufacture thereof
US4913259A (en) * 1987-12-16 1990-04-03 Minnesota Mining And Manufacturing Company Compressible ear tip
US4852684A (en) * 1987-12-16 1989-08-01 Minnesota Mining And Manufacturing Company Compressible ear tip
US4911993A (en) * 1988-02-01 1990-03-27 Eltech Systems Corporation Bipolar, filter-press, consumable metal anode battery
US4887348A (en) * 1988-03-09 1989-12-19 Tamminen Pentti J Alkalline cell battery and method for manufacture thereof
US5070787A (en) * 1988-06-24 1991-12-10 The Board Of Regents Of The University Of Texas System Method and apparatus for switching an electrical circuit
SE467165B (en) * 1988-10-28 1992-06-01 Nike Ab PRESSURE AIR PUMP DEVICE
US5008161A (en) * 1989-02-01 1991-04-16 Johnston Lowell E Battery assembly
US4997732A (en) * 1989-03-30 1991-03-05 Mhb Joint Venture Battery in a vacuum sealed enveloping material and a process for making the same
US4967136A (en) * 1989-09-25 1990-10-30 Prestolite Electric Incorporated Battery equalization circuit for a dual voltage charging system
DE3938262A1 (en) * 1989-11-17 1991-05-23 Asea Brown Boveri PROTECTIVE DEVICE FOR HIGH TEMPERATURE BATTERIES
US5070427A (en) * 1990-01-31 1991-12-03 Sparton Corporation Thermal switch for battery protection
CA2038354A1 (en) 1990-03-30 1991-10-01 William H. Kelly Ni-h2 battery having improved thermal properties
GB2244368A (en) * 1990-05-16 1991-11-27 Chloride Silent Power Ltd A thermal shunt for a battery contained in a thermally-insulated container
GB2248139A (en) * 1990-08-07 1992-03-25 Chloride Silent Power Ltd High temperature battery terminal provided with heat dissipator to prevent damage to cable insulation
US5089027A (en) * 1990-11-26 1992-02-18 Gould Inc. Method for producing a solid electrolyte cell
US5071652A (en) * 1990-12-11 1991-12-10 Globe-Union Inc. Metal oxide hydrogen battery having improved heat transfer properties
US5057385A (en) * 1990-12-14 1991-10-15 Hope Henry F Battery packaging construction
US5227264A (en) * 1991-02-14 1993-07-13 Hydro-Quebec Device for packaging a lithium battery
US5547775A (en) 1991-04-26 1996-08-20 Sony Corporation Circuit for preventing overcharge and overdischarge of secondary batteries
US5180641A (en) * 1991-05-09 1993-01-19 Rockwell International Corporation Battery cell bypass circuit
US5227259A (en) * 1991-07-24 1993-07-13 Electric Power Research Institute, Inc. Apparatus and method for locating and isolating failed cells in a battery
CA2051611C (en) * 1991-09-17 1996-01-23 Michel Gauthier Process for preparation of electrode collector systems for thin film generators, electrode collector systems et generators therefrom
US5199239A (en) * 1991-09-30 1993-04-06 Honeywell Inc. Housing seal interface
US5162171A (en) * 1991-10-28 1992-11-10 Globe-Union Inc. Metal oxide-hydrogen battery having modules extending longitudinally of the pressure vessel
WO1993011572A1 (en) * 1991-12-06 1993-06-10 Yuasa Corporation Thin battery and monolithic thin battery
DE4142628C1 (en) 1991-12-21 1993-05-06 Dieter Braun
US5197889A (en) * 1992-02-03 1993-03-30 Motorola, Inc. Electrical contact for battery package or similar device
US5283512A (en) * 1992-04-13 1994-02-01 Hughes Aircraft Company Charge balancing of batteries during charging
CA2068290C (en) * 1992-05-08 1999-07-13 Michel Gauthier Electrical connecting on lithium anodes
US5204194A (en) * 1992-05-21 1993-04-20 Magnavox Electronic Systems Company Multicell battery having a tab-fuse for overcurrent interruption
DE4218381C1 (en) 1992-06-04 1993-05-13 Daimler-Benz Aktiengesellschaft, 7000 Stuttgart, De
US5313152A (en) * 1992-06-19 1994-05-17 Ford Motor Company Network for minimizing current imbalances in a faradaic battery
US5385793A (en) * 1992-07-20 1995-01-31 Globe-Union Inc. Thermal management of battery systems
DE4225746A1 (en) 1992-08-04 1994-02-10 Hagen Batterie Ag Circuit device
US5300373A (en) * 1992-09-11 1994-04-05 Valence Technology, Inc. Electrochemical cell stack and method of making an electrochemical cell stack
US5530336A (en) 1992-09-17 1996-06-25 Sony Corporation Battery protection circuit
US5337042A (en) * 1992-09-28 1994-08-09 Chrysler Corporation Vehicle communications network transceiver, transmitter circuit therefor
US5478667A (en) 1992-10-29 1995-12-26 Shackle; Dale R. Heat dissipating current collector for a battery
US5363405A (en) * 1992-11-27 1994-11-08 Chrysler Corporation Vehicle communications network transceiver, bus driver therefor
US5354630A (en) * 1992-12-10 1994-10-11 Comsat Ni-H2 battery having improved thermal properties
JP3397351B2 (en) 1992-12-18 2003-04-14 キヤノン株式会社 Prismatic or sheet type battery and manufacturing method thereof
US5547780A (en) 1993-01-18 1996-08-20 Yuasa Corporation Battery precursor and a battery
US5409787A (en) * 1993-02-17 1995-04-25 Electrosource, Inc. Battery plate compression cage assembly
KR100306734B1 (en) 1993-04-05 2001-11-30 배리 이. 도이치 Battery Packs for Wireless Devices
JP3384027B2 (en) 1993-05-14 2003-03-10 ソニー株式会社 Charging method and charger
US5438249A (en) 1993-06-08 1995-08-01 Valence Technology, Inc. Method of state-of-charge indication by measuring the thickness of a battery
US5479083A (en) 1993-06-21 1995-12-26 Ast Research, Inc. Non-dissipative battery charger equalizer
US5595835A (en) 1993-07-22 1997-01-21 Japan Storage Battery Co., Ltd. Sealed type battery
AU691507B2 (en) 1993-09-17 1998-05-21 Nec Corporation Charging and discharging circuit for preventing overcharge and overdischarge of rechargable battery pack consisting of a plurality of rechargable batteries
US5393617A (en) * 1993-10-08 1995-02-28 Electro Energy, Inc. Bipolar electrochmeical battery of stacked wafer cells
US5478668A (en) 1993-11-30 1995-12-26 Bell Communications Research Inc. Rechargeable lithium battery construction
US5618641A (en) 1993-12-03 1997-04-08 Bipolar Power Corporation Bipolar battery construction
US5504415A (en) 1993-12-03 1996-04-02 Electronic Power Technology, Inc. Method and apparatus for automatic equalization of series-connected batteries
US5487958A (en) 1993-12-06 1996-01-30 Tura; Drew Interlocking frame system for lithium-polymer battery construction
DE69527735T2 (en) 1994-03-03 2002-12-05 Japan Storage Battery Co Ltd Safety arrangement for battery
DE4407156C1 (en) 1994-03-04 1995-06-08 Deutsche Automobilgesellsch Electric storage battery housing for electrically-driven automobile
JP3389670B2 (en) 1994-03-11 2003-03-24 日産自動車株式会社 Series connection circuit of secondary battery
US5346786A (en) * 1994-03-21 1994-09-13 Hodgetts Philip J Modular rack mounted battery system
JPH07263015A (en) 1994-03-24 1995-10-13 Yuasa Corp Lead-acid battery
US5670272A (en) 1994-03-31 1997-09-23 Valence Technology, Inc. Battery packaging for flat cell batteries having a compressing material for the cell stack
US5384212A (en) * 1994-04-25 1995-01-24 Globe-Union Inc. Flex-rib plaques for batteries
US5567539A (en) 1994-05-23 1996-10-22 Fuji Photo Film Co., Ltd. Non-aqueous secondary cell
DE4419281C1 (en) 1994-06-01 1995-12-14 Daimler Benz Ag High temperature battery
US5610495A (en) 1994-06-20 1997-03-11 Motorola, Inc. Circuit and method of monitoring battery cells
FR2721407B1 (en) 1994-06-21 1996-08-02 Renault Method and device for controlling the insulation of a direct current electrical network.
FR2722031B1 (en) 1994-07-04 1996-08-23 Accumulateurs Fixes REGULATOR DEVICE FOR ELECTRICAL BATTERY
JPH0823637A (en) 1994-07-06 1996-01-23 Mitsumi Electric Co Ltd Detection unit for protection circuit of rechargeable battery and protection circuit
US5548200A (en) 1994-07-06 1996-08-20 Norvik Traction Inc. Universal charging station and method for charging electric vehicle batteries
US5422200A (en) * 1994-07-27 1995-06-06 Hope; Stephen F. Battery packaging construction for alkali metal multicell batteries
US5503948A (en) 1994-08-02 1996-04-02 Microelectronics And Computer Technology Corporation Thin cell electrochemical battery system; and method of interconnecting multiple thin cells
JP2895757B2 (en) 1994-08-05 1999-05-24 日本ミクロコーティング株式会社 Polishing equipment
US5594320A (en) 1994-09-09 1997-01-14 Rayovac Corporation Charge equalization of series connected cells or batteries
US5622789A (en) 1994-09-12 1997-04-22 Apple Computer, Inc. Battery cell having an internal circuit for controlling its operation
DE4433836C1 (en) 1994-09-22 1995-11-09 Daimler Benz Ag Device for heating an interior of an electric vehicle
US5595839A (en) 1994-10-13 1997-01-21 Yardney Technical Products, Inc. Bipolar lithium-ion rechargeable battery
US5643044A (en) 1994-11-01 1997-07-01 Lund; Douglas E. Automatic chemical and mechanical polishing system for semiconductor wafers
US5633573A (en) 1994-11-10 1997-05-27 Duracell, Inc. Battery pack having a processor controlled battery operating system
US5619417A (en) 1994-11-23 1997-04-08 Chrysler Corporation Battery monitoring system for an electric vehicle
US5528122A (en) 1994-11-29 1996-06-18 Ventron Corporation Battery voltage equalizer circuit
GB2295718A (en) 1994-12-02 1996-06-05 Silent Power Gmbh Arrangements of batteries comprising an array of cells interconnected to give the required energy storage/operational voltage
US5600230A (en) 1994-12-15 1997-02-04 Intel Corporation Smart battery providing programmable remaining capacity and run-time alarms based on battery-specific characteristics
US5568039A (en) 1994-12-16 1996-10-22 Motorola, Inc. Apparatus and method of providing an initiation voltage to a rechargeable battery system
US5532087A (en) 1994-12-22 1996-07-02 Motorola, Inc. Electrochemical cell
US5623196A (en) 1994-12-27 1997-04-22 Motorola, Inc. Apparatus and method of simulating high battery temperature in a rechargeable battery
US5569550A (en) 1995-02-03 1996-10-29 Motorola, Inc. Battery pack having under-voltage and over-voltage protection
DE19503917C2 (en) 1995-02-07 1996-11-21 Mc Micro Compact Car Ag Electronic battery monitoring device
US5654622A (en) 1995-02-16 1997-08-05 Sanyo Electric Co., Ltd. Secondary battery charging method and apparatus which controls protecting voltage level of battery protecting circuit
US5563002A (en) 1995-02-21 1996-10-08 Motorola, Inc. Programmable battery
US5612153A (en) 1995-04-13 1997-03-18 Valence Technology, Inc. Battery mask from radiation curable and thermoplastic materials
US5593604A (en) 1995-05-04 1997-01-14 Motorola, Inc. Method of resistance welding thin elements
US5561380A (en) 1995-05-08 1996-10-01 Chrysler Corporation Fault detection system for electric automobile traction system having floating ground
US5650240A (en) 1995-08-21 1997-07-22 Hughes Aircraft Company Multicell battery system with individually controllable cell bypasses
US5556576A (en) 1995-09-22 1996-09-17 Kim; Yong C. Method for producing conductive polymeric coatings with positive temperature coefficients of resistivity and articles made therefrom
US5631537A (en) 1995-10-17 1997-05-20 Benchmarq Microelectronics Battery charge management/protection apparatus
US5534366A (en) 1995-11-22 1996-07-09 Motorola, Inc. Modular battery pack
US5626990A (en) 1996-02-02 1997-05-06 Portable Energy Products, Inc. Recombinant lead acid battery and method of making same
DE19618897B4 (en) 1996-05-10 2006-04-20 Varta Automotive Systems Gmbh Circuit arrangement for determining the insulation resistance of an accumulator battery
US6099986A (en) * 1997-07-25 2000-08-08 3M Innovative Properties Company In-situ short circuit protection system and method for high-energy electrochemical cells
JP2001223034A (en) * 2000-02-08 2001-08-17 Kubota Corp Temperature retaining structure of battery

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4383013A (en) * 1980-07-23 1983-05-10 Chloride Silent Power Limited High temperature multicell electrochemical storage batteries
JPS5991658A (en) * 1982-11-18 1984-05-26 Japan Storage Battery Co Ltd Monoblock container for alkaline storage battery
US4973936A (en) * 1989-04-27 1990-11-27 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Adminstration Thermal switch disc for short circuit protection of batteries
JPH0917416A (en) * 1995-06-30 1997-01-17 Fuji Elelctrochem Co Ltd Battery having explosion-proof function

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 008, no. 206 (E - 267) 20 September 1984 (1984-09-20) *
PATENT ABSTRACTS OF JAPAN vol. 097, no. 005 30 May 1997 (1997-05-30) *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6548206B1 (en) * 1997-07-25 2003-04-15 3M Innovative Properties Company In-situ short-circuit protection system and method for high-energy electrochemical cells
WO2007028803A1 (en) * 2005-09-06 2007-03-15 Dilo Trading Ag Special purpose lithium polymer batteries special purpose arrangements and method for prodcution thereof
WO2010037798A2 (en) * 2008-09-30 2010-04-08 Magna Steyr Fahrzeugtechnik Ag & Co Kg Energy accumulator module
WO2010037798A3 (en) * 2008-09-30 2011-01-13 Magna Steyr Fahrzeugtechnik Ag & Co Kg Energy accumulator module
CN102203979A (en) * 2008-09-30 2011-09-28 玛格纳E-汽车系统有限两合公司 Energy accumulator module
US9673479B2 (en) 2008-09-30 2017-06-06 Samsung Sdi Co., Ltd. Energy accumulator module

Also Published As

Publication number Publication date
JP4267812B2 (en) 2009-05-27
CA2297839C (en) 2010-01-12
US6099986A (en) 2000-08-08
CA2297839A1 (en) 1999-02-04
US6548206B1 (en) 2003-04-15
JP2001511635A (en) 2001-08-14
AU8510998A (en) 1999-02-16
EP1021850A1 (en) 2000-07-26

Similar Documents

Publication Publication Date Title
CA2297839C (en) In situ short-circuit protection system and method for high-energy electrochemical cells
EP0998766B1 (en) Thermal conductor for high-energy electrochemical cells
EP0998765B1 (en) Thermal management system and method for a solid-state energy storing device
US6641942B1 (en) Solid-state energy storage module employing integrated interconnect board
RU2468477C2 (en) Accumulator battery of middle or large size of increased security
US20060076923A1 (en) Methods and systems for assembling batteries
EP1479127A2 (en) Temperature control apparatus and method for high energy electrochemical cells
KR20070012937A (en) Secondary battery with ptc device
EP1018179A1 (en) Pressure system and method for rechargeable thin-film electrochemical cells
US5948556A (en) Massively parallel spacecraft battery cell module design
US5993993A (en) Unregulated spacecraft electrical bus
KR101731314B1 (en) Battery Module for Secondary Battery
JP7325890B2 (en) Battery modules and battery packs containing the same
US20220238934A1 (en) Battery Module and Battery Pack Including the Same
US20240106023A1 (en) Cell busbar fuse with direct cooling
US20230268583A1 (en) Battery
WO2024063955A1 (en) Cell busbar fuse with direct cooling
KR102308168B1 (en) Battery module, battery pack including the same, and vehicle including the same
KR20220075045A (en) Battery module and battery pack including the same and vehicle including the same

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GE GH HU ID IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG UZ VN YU ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
ENP Entry into the national phase

Ref document number: 2297839

Country of ref document: CA

Ref country code: CA

Ref document number: 2297839

Kind code of ref document: A

Format of ref document f/p: F

NENP Non-entry into the national phase

Ref country code: KR

WWE Wipo information: entry into national phase

Ref document number: 1998935973

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 1998935973

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 1998935973

Country of ref document: EP