CA1178824A - Gas sensor - Google Patents

Gas sensor

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Publication number
CA1178824A
CA1178824A CA000387383A CA387383A CA1178824A CA 1178824 A CA1178824 A CA 1178824A CA 000387383 A CA000387383 A CA 000387383A CA 387383 A CA387383 A CA 387383A CA 1178824 A CA1178824 A CA 1178824A
Authority
CA
Canada
Prior art keywords
conductive strip
film
conductive
dielectric film
semiconductive
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
CA000387383A
Other languages
French (fr)
Inventor
Leslie J. Rigby
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ITT Inc
Original Assignee
ITT Industries Inc
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 ITT Industries Inc filed Critical ITT Industries Inc
Application granted granted Critical
Publication of CA1178824A publication Critical patent/CA1178824A/en
Expired legal-status Critical Current

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/12Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a solid body in dependence upon absorption of a fluid; of a solid body in dependence upon reaction with a fluid, for detecting components in the fluid

Abstract

L. J. Rigby lX

GAS SENSOR

ABSTRACT OF THE DISCLOSURE

A semiconductor gas sensor comprises an insulating substrate on which a resistive heater track coupled to a pair of electrodes is deposited. A film of a semiconductive metal oxide. typically a doped oxide, is ion-plated onto the assembly so as to contact the resistive track and a further electrode. Exposure of the device to a particular gas, e.g.
hydrogen sulphide, reduces the resistivity of the semiconductive film, this change being detected via an amplifier circuit. In an alternative version of the sensor, the heater is disposed under a dielectric layer, the semiconductive film being ion-plated onto the dielectric layer and electrodes therein.

Description

'7~8;24 - 1 - L. J. Rigby lX

GAS SENSOR

BACKGROUND OF THE INVENTION
This invention relates to semiconductor gas sensors and to methods of fabrication of such sensors.
PRIOR ART STATEMENT
The detection and measurement of toxic gases is an important problem in industry. Some gases, for example hydrogen sulphide, are extremely poisonous and it is therefore essential to provide a detection system that provides reliable measurement at concentrations as low as 1 to lO parts per million. A number of detection techniques for toxic gases have been described. Analytical techniques, such as gas chromotography and absorption/titration are of course both accurate and reliable at these low concentrations but suffer from the disadvantage that the equipment involved is both bulky and delicate. Furthermore, the response time inherent in these techniques is relatively long and thus renders them unsuitable for providing a continuous series of readings. In an attempt to overcome these disadvantages semiconductor gas sensors have been developed. Sensors of this type include a thin film of a semiconductive material, typically a metal oxide, deposited on an insulating substrate. The material is such that its electrical resistance changes in the presence oP traces of the toxic gas under investigation, this change in resistance being monitored via an amplifier. While such devices are portable and have a relatively rapid response time they suffer from the disadvantage that present manufacturing methods produce devices with a wide range of electrical characteristics. This necessitates a relatively large investment in testing equipment and quality control.
SUMMARY OF THE INVENTION
According to one aspect of the present invention, a hydrogen sulphide gas sensor comprises: a substrate insulator: first and second parallel conductive strips forming electrodes affixed to said substrate insulator in -- 1 -- ~
- 2 - L. J. Rigby lX

spaced relation to each other; a layer of a resistive heater material affixed to said substrate insulator and to said first and second strips; a dielectric film having obverse and reverse sides, said dielectric film having said reverse side thereof covering and fixed relative to said resistive heater material; third and fourth conductive strips forming electrodes, said third and fourth conductive strips being fixed to the obverse side of said dielectric film, said third and fourth conductive strips being long and thin in comparison to their widths, said third conductive strip being straight, said fourth conductive strip being U-shaped and straddling said third conductive strip, said fourth conductive strip having one leg on each of and parallel to said third conductive strip, said legs being connected by a bight portion, each of said legs being uniformly spaced from said third conductive strip; and a semiconductive film fixed to said dielectric film between and in contact with said third and fourth conductive strips in a position to be heated by said heater means, said semiconductive film having a resistivity which decreases with an increase of hydrogen sulphide concentration in a gas contacting the same, said semiconductive film comprising tin oxide doped with alumina.
According to another aspect of the invention, there is provided a gas sensor comprising: a substrate insulator;
a dielectric film having obverse and reverse sides; heater means fixed relative to and on said reverse side to supply heat to the vicinity of said obverse side; first and second conductive strips forming electrodes, said first and second conductive strips being fixed to the obverse side o~ said dielectric film, said first and second conductive strips being long and thin in comparison to their widths, said first conductive strip being straight, said second conductive strip being U-shaped and straddling said third conductive strip, said second conductive strip having one leg on each side of said first conductive strip, said legs
- 3 - L. J. Rigby lX

being connected by a bight portion, each of said legs being uniformly spaced from said third conductive strip: and a semiconductive film fixed to said dielectric film between and in contact with said first and second conductive strips in a position to be heated by said heater means, said semiconductive film having a resistivity which decreases with an increase of hydrogen sulphide concentration in a gas contacting the same.
BRIEF DESCRIPTION OF THE DRAWINGS
In the accompanying drawings which illustrate exemplary embodiments of the present invention:
Fig. 1 is a plan view of one embodiment of a semiconductor gas sensor device;
Fig. 2 is a cross-section of the device of Fig. l;
Fig. 3 is a block diagram of a gas measurement circuit incorporating the sensor of Figs. 1 and 2:
Fig. 4 is a schematic diagram of an ion-plating apparatus for fabricating the device of Figs. 1 and 2:
Figs. 5a and 5b show, in plan views, successive stages in the manufacture of a second embodiment of semiconductor gas sensor device: and Fig. 6 shows a variation of the embodiment of Figs. 5a and 5b as mounted on a lZ pin T08 header.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
Referring to Figs. 1 and 2, a semiconductor gas sensor includes an insulating, typically alumina, substrate 11 on which an array of precious metal electrodes 12, 13, 14 is deposited. &old or gold alloy electrodes are preferred as these materials are both chemically inert and relatively easy to apply. Typically the electrodes are formed by deposition of thick film inks followed by firing, or by vacuum evaporation. As can be seen from Fig. 1 the electrode array comprises a pair of relatively small electrodes 12, 14 with an elongate electrode 13 disposed therebetween.

2~
- 4 -- L. J. Rigby lX

A substantially U-shaped resistor track 15 is next deposited on the substrate such that the ends of the track contact the electrodes 12 and 14 respectively with the elongate electrode 13 being disposed between but spaced from the two limbs of the U. This resistor track may be applied by the conventional technique of printing the track with a conductive ink, deposited through an in-contact mask, followed by firing of the ink. Such techniques are well known in the art and need not be further described.
The structure is next overlaid with an ion-plated film 16 of a semiconductive metal oxide deposited from a radio frequency plasma containing the metal in vapor form together with an exces6 of an oxidizing vapor and optionally one or more dopants for controlling the electrical characteristics of the film 16. The active region of the device is provided by the portion of the film 16 disposed between the elongate electrode 13 and the U-shaped resistor track 15. Preferably the film 16 comprises tin oxide doped with alumina and provided by electron bombarding a 0.1%
aluminum alloy of tin into a radio-frequency oxygen plasma discharge. The tin and aluminum are oxidized in the plasma and so form a layer of doped tin oxide on any solid surface exposed to the plasma. Such a film has been found to be highly specific to hydrogen sulphide.
In a preferred construction the reverse face of the substrate 11 is coated with a layer of gold formed e.g. by painting or printing with a gold ink followed by firing at 850C in air for about 10 minutes. This layer allows the sub6trate to be soldered to the surface of a 6uitable holder 6uch as a dual-in-line (DIL) circuit package 17. The electrodes 12, 13 and 14 of the device can then be coupled to respective output pins 1~ via ultrasonically bonded contact wires 19.
In use a steady current is passed from a constant current source 31 (Fig. 3) through the resistor track via 8~
- 5 - L. J. Rigby lX

the electrodes 12 and 14 so as to maintain the device, and hence the metal oxide film 16. at an elevated temperature.
Typically the current is controlled so as to maintain the device at 280C as it has been found that at this temperature the device has a fast response time and has a high selectivity to hydrogen sulphide gas. The resistance of the metal oxide film between the elongate electrode 13 and the resistor track is monitored via an amplifier 32 coupled to an output/display device 33. Exposure of the detector to the gas, e.g. hydrogen sulphide, causes a drop in the resistance of the metal oxide film, this resistance drop being a function of the gas concentration.
An apparatus for ion-plating the metal oxide film is shown in Fig. 4 of the accompanying drawings. The apparatus includes a vacuum chamber defined by a glass bell jar 41 supported on a metal base plate 42. The chamber is evacuated via pipe 43 and reactant gases are supplied to the chamber via pipe 44. An electron gun 45 is mounted within the chamber and is directed towards a body 46 of the metal whose oxide is to be deposited. Typically this metal body 46 comprises a 0.1% aluminum tin alloy.
Radio-frequency energy is supplied via electrode 47 from a generator 48.
To deposit the oxide film the chamber is evacuated and back filled with oxygen at a reduced pressure. The generator 47 is switched on to initiate a glow discharge or plasma into which the metal is then electron beam evaporated from the body 46. The metal vapor reacts with the oxygen plasma and a film of oxide is deposited on a plurality of workpieces 49 disposed radially arouna the metal body. We have found that to prevent the risk of deposition of unoxidized metal the workpieces 49 should be at least 50mm from the metal body and in positions that are not in a line of sight with the electron beam target region. Typically we employ a 70ma electron beam current together with an oxygen pressure of 10 5 torr. for a period of 20 min. This gives a film thickness of 1,000 to 3,000 ~.
- 6 - L. J. Rigby lX

The embodiment of Figs. 5a and 5b employs a different heater structure to that employed in the Figs. 1 and 2 embodiment. The semiconductor gas sensor includes an insulating, typically alumina, substrate 50 on which two precious metal electrodes 51 and 52 are deposited.
Typically the electrodes are of gold applied by means of a thick film ink deposition followed by firing. A heater strip 53 formed, for example, from Dupont 1411 thick film ink, is deposited on the substrate 50 such that opposite ends thereof contact the electrodes 51 and 52 respectively and subsequently fired. A dielectric glass layer 54 is then applied by thick film techniques to cover the heater strip 53 and the electrodes apart from contact pad areas 55 thereof and subsequently fired. An array of electrodes 56, 15 57, 58 are then applied on the dielectric film 54 to extend over the heater strip 53. Typically these electrodes are of gold and are provided by a conventional thick film technique and subsequent firing.
The center electrode 56 is equivalent to the elongate electrode 13 of Fig. 1, the intermediate electrode 57 is equivalent to the resistor track 15 of Fig. 1 for the purposes of measuring the resistance of the metal oxide film between the center electrode 56 and the intermediate electrode. The outer electrode 58 comprises a guard electrode for screening purposes.
Preferably the reverse face of the substrate 50 is coated with a layer of gold, as described with reference to substrate 11, to facilitate soldering to the surface of a suitable holder. After mounting to such a ho}der the 30 electrodes 51, 52, 56, 57 and 58 are electrically connected to respective output pins by suitable connection wire techniques.
An ion-plated film (reference numeral 60 in the Fig. 6 variation of Figs. 5a and 5b) of a semiconductor metal oxide, such as alumina doped tin oxide, is then ~ 2~ 7 - L. J. Rigby lX

deposited by the process described above to cover all exposed regions of the substrate and the various layers thereon. Alternatively the sensor film 60 may be deposited prior to mounting of the substrate on a holder, and S attachment of the interconnection wire~, in which case the film 60 would be deposited through a suitable mask so that the wire connection etc., can be performed subsequently to portions of the electrodes not coated with the sensor film.
In the Fig. 6 variation of the Figs. 5a and 5b embodiments, the electrodes 56. 57 and 58 are orientated at 90 to those shown in Fig. 5b in order to facilitate mounting to a 12 pin T08 header 59. The embodiment of Fig. 6 also includes a thermistor 61. Typically the thermistor 61 i8 a micro bead thermistor mounted on the surface of the device by melting the lead glass bead thereof into part of the thick film dielectric glass coating 54.
The thermistor is employed for temperature control purposes so that the device can be operated accurately at ambient temperatures varying from ~20 to +30C. The thermistor comprises the control sensor for a heater power supply circuit (not shown in Fig. 6).
The use of the isolated (under dielectric) low resistivity, typically lOQ, heater allows uniform heating of the sensor film to be obtained at low voltage and with low power consumption. At 20C ambient temperature 4 watts at 6 volts enables a 280C operating temperature to be achieved, in comparison with 4 watts at 12 volts for a device of the Fig. 1 construction, which requires a drop of 12 volts across the heater to obtain a 280C operating temperature and a further 12 volts to the measuring electrode. Thus battery powered sensors can be employed, which are of particular relevance to the use of sensors in potentially flammable atmospheres and/or in remote locations.
The isolating thick film dielectric layer 54 covering the film heater 53 provides a more uniform surface 1~ 7~ 8 - L. J. Rigby lX

for the sensor film 60 to be deposited on than the alumina substrate of the Fig. 1 embodiment and this allows thinner sensor films, typically less than 500 A (50nm) to be deposited with good adhesion, continuity and stable resistivity in dry air.
The geometry of the thick film gold electrodes allows easily measurable electrical currents to flow from a low voltage source across 50 nm sensor films of 1 to 10 ohm cm resistivity. Typically the sensor resistances are lOMohms or less at 280C in dry air, falling to O.SMohms or less when exposed to lOppm of hydrogen sulphide.
Ion-plating of doped tin oxide on a cold substrate provides a sensor film of controlled discontinuity. Low surface temperatures reduce the surface kinetic energy of the adhering atoms and/or radicals which minimizes surface mobility and results in a maximum number of localized surface discontinuities. Thus choice of the surface temperature during film deposition optimizes the concentration of surface sites for gas absorption and reaction without impairing the stability of the sensor resistance.
The ion-plated sensors described above show excellent sensitivity to hydrogen sulphide at temperatures as high as 280C. The response to sulphur dioxide is generally 1000 times less, and the relative sensitivity to hydrogen is 1000 times less than for hydrogen sulphide.
The fastest response to and recovery from hydrogen sulphide exposure is obtained at temperatures of the order of 280C. As the operating temperature of the sensor film is reduced, sensitivity, response and recovery are increasingly impaired. The evaporation of a thin layer of platinum on the surface of the sensor greatly improves the recovery of the device at lower temperatures. However, high temperature operation is preferred since this is considered to minimize the affect of absorbed moisture on the sensor devices.

11'7~8~:4 - 9 - L. J. Rigby lX

At temperatures higher than 280C the sensor becomes more sensitive to other sulphur compounds, for example sulphur dioxide, so that in the absence of hydrogen sulphide and at 350C, for example, reasonable selectivity to these other sulphur compounds can be obtained in the presence of flammable gases such as hydrogen, carbon monoxide, methane and other hydrocarbons.
The following example illustrates the invention.
Using the apparatus of Fig. 4 a plurality of devices having the structure shown in Figs. 1 and 2 (device Nos. A2 to B6) or the structure shown in Fig. 6 (device Nos.
Cl to C5) were fabricated. Each device was electrically heated to a temperature of 280C and its film resistance measured in air (Ro) and in an air atmosphere containing 10 parts per million of hydrogen sulphide (R10). The results are summarized in the following table.
(treS is the time taken for the initial resistance (Ro) to be halved (values taken to nearest 0.1 of a minute) when exposed to 10 ppm of H2S.) .
20 ~evice Film Ro (MQ) R10 (MQ) Ro~R10 R10 treS
No.Thickness resistivity in R in Qcm A.22300-3000 O.OZ2 0.001413.8 0.11 0.2 A.3 " 0.025 0.00208.5 0.15 0.3 A.4 " 0.175 0.007723.8 0.50 0.3 A.5 " 0.291 0.009833~3 0.74 0.2 A.6 " 0.203 0.007928.9 0.59 0.2 B.l1000-1200 0.074 0.004528.4 0.16 0.3 B.2 " 0.090 0.006422.3 0.23 0.3 B.3 " 0.053 0.003223.4 0.12 0.3 B.4 " 0.063 0.003720.1 0.13 0.3 B.5 " 0.020 0.00316.5 0.11 0.9 B.6 " 0.020 0.00209.9 0.07 0.8 C.l500 6.8 0.31 22 6.2 0.2 C.2 " 5.6 0.15 37 3.1 0.2 C.3 " 6.0 0.20 30 4.1 0.2 C.4 " 9.6 0.55 17 11.4 0.2 C.5 " 4.5 0.18 25 3.9 0.2 g 82~
- 10 - L. J. Rigby lX

These results illustrate the feasibility of producing gas sensor devices by the methods described herein.
While the sensor devices described herein are specific to hydrogen sulphide at 280C it will be appreciated that specificity to other gases may be provided by using other temperatures or by ion-plating an appropriate semiconductive metal oxide to provide the active region.

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~ 12 -These reslllts illustxate t,he feasib,ility o;~
producing gas sensor devices by the methods described herein.
Whi.lst the sensor devices described herein are specific ~o hydrogen sulphide at 280C it will be appreciated that specificity to o~her gases may be provided by using o-ther temperatures or by ion-plating an apprvpriate semiconductive metal oxidc- t.o pro~-iae the active region.

.

.

Claims (3)

WHAT IS CLAIMED IS:
1. A hydrogen sulphide gas sensor comprising: a substrate insulator; first and second parallel conductive strips forming electrodes affixed to said substrate insulator in spaced relation to each other; a layer of a resistive heater material affixed to said substrate insulator and to said first and second strips; a dielectric film having obverse and reverse sides, said dielectric film having said reverse side thereof covering and fixed relative to said resistive heater material; third and fourth conductive strips forming electrodes, said third and fourth conductive strips being fixed to the obverse side of said dielectric film, said third and fourth conductive strips being long and thin in comparison to their widths, said third conductive strip being straight, said fourth conductive strip being U-shaped and straddling said third conductive strip, said fourth conductive strip having one leg on each of and parallel to said third conductive strip, said legs being connected by a bight portion, each of said legs being uniformly spaced from said third conductive strip; and a semiconductive film fixed to said dielectric film between and in contact with said third and fourth conductive strips in a position to be heated by said heater means, said semiconductive film having a resistivity which decreases with an increase of hydrogen sulphide concentration in a gas contacting the same, said semiconductive film comprising tin oxide doped with alumina.
2. The invention as defined in claim l, wherein a fifth conductive strip is affixed to said dielectric film, said fifth conductive strip being U-shaped and surrounding said fourth conductive strip.
3. A gas sensor comprising: a substrate insulator; a dielectric film having obverse and reverse sides; heater means fixed relative to and on said reverse side to supply heat to the vicinity of said obverse side;
first and second conductive strips forming electrodes, said first and second conductive strips being fixed to the obverse side of said dielectric film, said first and second conductive strips being long and thin in comparison to their widths, said first conductive strip being straight, said second conductive strip being U-shaped and straddling said third conductive strip, said second conductive strip having one leg on each side of said first conductive strip, said legs being connected by a bight portion, each of said legs being uniformly spaced from said third conductive strip; and a semiconductive film fixed to said dielectric film between and in contact with said first and second conductive strips in a position to be heated by said heater means, said semiconductive film having a resistivity which decreases with an increase of hydrogen sulphide concentration in a gas contacting the same.
CA000387383A 1980-10-07 1981-10-06 Gas sensor Expired CA1178824A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8032248 1980-10-07
GB8032248A GB2085166A (en) 1980-10-07 1980-10-07 Semiconductor gas sensor

Publications (1)

Publication Number Publication Date
CA1178824A true CA1178824A (en) 1984-12-04

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CA000387383A Expired CA1178824A (en) 1980-10-07 1981-10-06 Gas sensor

Country Status (3)

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US (1) US4399424A (en)
CA (1) CA1178824A (en)
GB (1) GB2085166A (en)

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Publication number Publication date
US4399424A (en) 1983-08-16
GB2085166A (en) 1982-04-21

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