CA1213662A - Organic electroluminescent devices having improved power conversion efficiencies - Google Patents
Organic electroluminescent devices having improved power conversion efficienciesInfo
- Publication number
- CA1213662A CA1213662A CA000428167A CA428167A CA1213662A CA 1213662 A CA1213662 A CA 1213662A CA 000428167 A CA000428167 A CA 000428167A CA 428167 A CA428167 A CA 428167A CA 1213662 A CA1213662 A CA 1213662A
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- Canada
- Prior art keywords
- bis
- hole
- zone
- benzoxazolyl
- carbon atoms
- Prior art date
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- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/22—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/652—Cyanine dyes
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/655—Aromatic compounds comprising a hetero atom comprising only sulfur as heteroatom
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
Abstract
ORGANIC ELECTROLUMINESCENT DEVICES HAVING IMPROVED
POWER CONVERSION EFFICIENCIES
Abstract Electroluminescent devices are disclosed com-prising a hole-injecting zone and an adjacent organic luminescent zone, the device having a power conversion efficiency of at least 9 X 10-5 w/w and said zones having a combined thickness no greater than about 1 micron.
POWER CONVERSION EFFICIENCIES
Abstract Electroluminescent devices are disclosed com-prising a hole-injecting zone and an adjacent organic luminescent zone, the device having a power conversion efficiency of at least 9 X 10-5 w/w and said zones having a combined thickness no greater than about 1 micron.
Description
ORGANIC ELECTROLUMINESCENT DEVICES HAVING IMPROVED
POWER CONVERSION EFFICIENCIES
1) Field of the Invention Thi~ invention relate to electroluminescent devices tha~ generate light in response ~o an electrlc signal, wherein organic compounds are the light-generating means.
POWER CONVERSION EFFICIENCIES
1) Field of the Invention Thi~ invention relate to electroluminescent devices tha~ generate light in response ~o an electrlc signal, wherein organic compounds are the light-generating means.
2) Background of the Invention For organic electroluminescent device~ to become fully competitive with their ~norgani~ counter-parts, it i6 desirable that their power conversion efficiencies be increased at competitive co~ts. The power conver~ion efficiency i6 defined a~ the ratio of power output to power input, usually watt per watt, and is a function of the driving voltage of the device. For driving voltages ~hat utilize economical drive cir-cuitry, that is, voltages no greater than 25 volt~, power conversion efficiencles h~ve been limited to no more than 1 X 10- 5 W/W in organic device~. Organic electroluminescent devices using thick films (> 5~), or single cry~tals, have been produced with power conver~ion efficiencies greater than 10-5 w/w.
However, because of their greater thickness, the voltage required to drive ~uch devices i~ quite high (~ 100 ~5 Vol~s).
In order to reduce the driving voltage to no more than about 25 volts, thin-film electroluminescent device6 are desirable, which as used herein means a device wherein the thickne~s of the active zones or layers, that i8 ~ the material between the electrodes, does not exceed about 1 micron. The thin film format has been particularly difficult to achleve ln light of a pinholing problem. Pinholes are unacceptable because they 6hort out the cell-- see e.g., Dresner, RCA Review, Vol. 30, p. 322ff (June 1969), and especially p. 326.
To prevent formation of pinholes, a binder has been ,~.
conventionally used in the coating formulations.
Example6 of such binderR include add$tion polymers ~uch as polystyrene, and condensation polymers such as polyesters. Although shorting of the cell may be avoided, the use of a binder i8 sometimes unsatisfactory. It require~ the use of solvent coating manufacturing techniques, and the solvent of the one layer may also act a~ a solvent for the underlayer, thu~
preventing a sharp demarcation between layer~. Although one could imagine a process of solvent-coating the one layer that needs a binder and then vapor depositing the layer(s) not needing a binder, a reverse sequence in which the luminescent layer i~ solvent-coated has not proven to be practical when the solvent affects the lower layer.
The cells de6cr~bed in commonly owned U.S.
Application Serial No. 169,705, filed on July 17, 1980, by C. W. Tang entitled "~rganic Electroluminescent Cell", now U.S. Patent No. 4,356,429, are examples of markedly improved devices of the thin film format. Such cell6 have improved power conversion efficiencies by reason of reduced thicknes6 of the luminescent zone, and of the use of an ad~acent hole-in~ecting zone.
Although the cells of the aforesaid application have demonstrated the noted marked improvement over prior art cells, they have not achieved the levels of power conver~ion efficiencies that have been desired, that i~, at least 9 X 10-5 w/w or higher when using a driving voltage no greater than 25 volts. The por-phyrinic compounds in the hole-in~ecting layer are colored and thus tend to undesirably absorb some of the light th~t is emitted by the cell. Also, the por-phyrinic compounds appear to interfere with the efficient radiative recombination of holes and electrons needed to efficiently generate light output.
12136~2 Thus, what ha6 been needed prior to thi6 invention is an electroluminescent, hereinafter, "ELI', device that has power conver~ion efficiencie~ improved by at least one order of magnitude, i.e., to at least 9 X 10-5 w/w, while maintaining the thin film format and reduced driving voltages.
S~MMARY OF THE INVENTION
In accordance with the present invention there is advantageously featured an organic electroluminescent device that haæ the sought-after improved power conver-~ion efficiency as well a8 a thin film format wherein the combined thickness of the act~ve ~ones doe6 not exceed about 1~.
It i8 another advantageous feature of the invention that the luminescent zone or the hole-in~ecting zone o~ such a device is manufacturable from an electron-transporting compound or from a hole-tran~porting compound, respectively, which in many embodiments of the invention is sccomplished without a binder in the respective zone.
Still another advantageou~ feature of the invention is that compounds hflve been discovered for the hole-in~ecting layer that are subgtantially transparent to the generated radiation.
The aforesaid features of the invention result from the following more specific aspects of the inven-tion: In sccord with one aspect, an electroluminescent deYiCe i6 provided comprising, in sequence, an anod~
electrode, a hole-in~ecting zone, A lumine6cent zone, and a cathode electrode, wherein at least one of the electrodes transm~ts at least 80% of radiation having wsvelengths longer than 400 nm. Thi~ device is improved to have a power conversion efficiency of at least 9 X 10 5 w/w and said zones have a combined thickness of no greater than about 1 micron.
Most preferably, the luminescent zone of the afore~a~d device comprises a electron-transporting ;
4 lZ~;~662 compound that provideæ an electroluminescent quantum efficiency of at least about 5 X 10-~ pho-tons/electron, when used in a teæt device driven at no more than the le6ser of i) 25 volts snd ii) the voltage which produces the maximum power conver~ion efficiency of ~aid device, the test device comprising 1) a hole-in~ecting zone consi~ting essentially of l,l-bi6(4-di-p-tolylaminophenyl~cyclohexane, such hole-in3ecting zone and ~aid luminescent zone hav~ng a combined 10 thicknes~ of no more than 1~, 2~ an anode electrode $hat transmits at least 80a of radiation having wavelengths longer than 400 nm, and 3) an indium cathode.
Other advantageous features of the invention will become apparent upon reference to the following Description of the Preferred Embodimen~s when read in light of the attached drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a partially schematic section view of a device of the invention connected to a power source;
20 and Fig. 2 iB a log-log graph of power convergion efficiences vs. electroluminescent quantum efficiencies for devices produced in accordance with the invention.
DESCRIPTION OF THE PREFERRED EMBODIMEWTS
This invention i8 described particularly in connection with embodiments wherein the materials of the electroluminescent device are in layers or laminae, one on top of the other. In addition, the invention is applicable to an electroluminescent (hereinafter, "EL") cell or device wherein the hole-transporting material and the luminescent material are in zones, whether the zones are in layers or otherwise.
The device of this invention compri6es a hole-in3ecting layer and a luminescent layer. ~he 35 hole-in3ecting layer comprises a hole-transporting compound, while the luminescent layer comprises an electron-tran6porting compound.
~2136~2 We have discovered that there are certain electron-transporting compounds that produce EL quantum efficiency values in exces~ of 5 X 10-~ pho-tons/electron, when u~ed in a cell driven and con6tructed ~s herein~fter described. Because of the direct relationship which occurs between power conver-sion efficiencies and EL quantum efficiencie6, these compounds insure that for the drivlng vol~age noted, the power conver~ion efficiency will be at least 9 X 10-5 w/w. Because these compounds are readily deposited in a thin film format, a thin-film device i8 readily obtain-able wherein the combined thickness of the active zones doe6 not exceed 1~.
As u6ed herein, an electron-tran6porting com-pound i6 a compound that i8 reducible in an oxidation-reduction reaction. It is tho~e electron-transporting compounds producing at least 5 X 10-~ EL quantum efficiency, a6 per the te6t hereinafter defined, that are parti~ularly useful in thi6 invention. (As is well known, the EL quantum efficiency simply equals the ratio of photon6 per second emitted from the cell, to the electrons per second measured in the external circuit.
This efficiency is not to be confused with power conversion efficiency, which is defined in units of watt/watt.) To determine whether an electron-transporting compound produces an EL quantum efficiency at least equal to 5 X 10-~ photons/electron (or O.OSa), the following test i6 conducted:
An EL cell i8 constructed in the following ~equence: an anode electrode that transmits at least 80% of radiation having wavelengths longer than 400 nm, a hole-in~ecting layer consisting essentially of 1,1-bis(4-di-p-tolylaminophenyl)cyclohexane, a layer of the electron-transporting compound in question, a~d an indium cathode, wherein the hole-in~ecting layer and the -6- 1 Z ~ 3 6 ~ Z
luminescent l~yer together do not exceed 1~ in thick-ness. A driving voltage i~ spplied, and iB increa6ed until either the maximum power conversion efficiency, or 25 volts, is reached, whichever occurs first. The maximum EL quantum efficiency i~ measured at thi6 voltage.
Table I illustrates the EL quantum efficiencies for 60me u6eful electron-transporting compounds, when tested in the device constructed aR noted and driven at the noted voltage6. For each of these examples, the voltage of the maximum EL quantum efficiency was less than the 25-volt limit.
-7- ~ Z1366Z
~ ~o c C
? JJ Cg C u~
)~ o C o oo Q
~t ~ P1 ~ ~
e ~ ~ o , eO ~ o o o o o o o lU
E o~
X ~ ~ ~ ~ ~ K U~ X
C~ ~ ~ X
~ q~
E~
~ 04 D O' V
D 1~ C
C ~ ~ ~
o ~ o o o o o o , O `~
C ~
o ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ C
.C ~ ~ _ O :C CO ~ ~ ~ ~ o X .~CO
v Q~ o c~ a 0 ~ ~ ~ ~ v ~0 ~: ~ C ~ C ~ C t~ C ~ g ~ ~
C ~ C ~ ~ ~ C ~ C ~ C ~ C ~
JJ _ ~ 1~ l H 1-1 O
~ g ~ ~ o ~ eO ~ eO ~ g ¢ eO ¢ 8 ~ 80 ~ ~
M ~ C ' E3 ~ 3 ~ O ~I O ~I O ~-I O ~ O ~ O ~
~ ~ ~ ~ v ~ J~ n v u~ J~ Lr, J~ v u~ e 4~ ~ _1 x ~ ~ 3 O ~ ~ _ Z :Z Z Z Z Z :~ Z ~lt -8~ 13~6Z
V' X ~
i \ ~ ~ ~
// tD
0 ~
~ ~ o _~ N
t) 0 / ~ O
N
C
.C
O
C
/ _l .=. ~ ~ I I
O =- ~ O ~//
= V
_ Z/ ~-= O .,~ // \ ~ ~
=- ~ Z;D 5 El o--- 0 ~ --~
O ~
_1 ~ 0 P
_I ~ I
1213~62 ~C
_, .~, _, ._ .=.
:~ o o ;\ /;
o;\ /; N
~ =- C.~ :C U ; ~ \ f ) N E3 -- IZ~ / N I S w C
Z ~ I G / ~ O
r~ ~ ; . c . ~Y ~ \/~
C
.=. , ~ . ~ ~ ~ o ~ . C
.=. ~ ~ // ~ .c o . - . ~ 0 ~: 0 .D C~
~ ~ w -lo- lZ1366Z
/ ~ ~U ~
.
_~ ~ N
~; ~ N ~ ~ X X
N =. X ~3 C
Z~ f ~ ~
.=. :>~ ;=. 1 ,D
~ =- U~ ,~
=- V / \ /
=- ~
0 C~ ~ 0 o `~
~ - ~ 0 ~
Hole-transporting compound6 of the hole-in3ecting layer, as used herein, Are compounds which, when disposed between two electrode6 to which a field is applied, and a hole is in~ected from the anode, S permit adequate transport of holes to the cathode electrode. More ~pecifically, a compound i~ defined to be hole-transporting if it ha6 a hole mobility factor of at least 10-6 cm2/volt-sec when a layer i8 dispo~ed between electrodes to which an electric field of 10 to 10 6 volt6/cm is applied. It ha6 been found thst the most preferred hole-transporting compounds are aromatic amine~ that are readily and rever6ibly cxidiz-able~
Mo~t preferably, the hole-in~ecting layer i8 the trsnsparent portion of the active layers, becau6e i~
is ad~acent to the transparent electrode. Thus, the hole-transporting compound is al60 preferably at least 90% transmissive at 400 nm, or longer, wavelengths.
That iB, the hole-transporting compound is preferably essentially colorless.
Preferred examples of useful hole-transporting compound R that have the afore-noted light transmittance include amines that are solid at room temperature and in which at least one nitrogen atom is tri-~ubstituted with substituents at least one of which is aryl. As will be apparent from the examples that follow, "aryl" sub-stituents in hole-transporting compounds includes substituted aryl as well as unsubstituted aryl, such as phenyl and methylphenyl. Examples of u~eful substi-tuents include alkyl of 1 to 5 carbon atoms, for exam-ple, methyl, ethyl, propyl, and the like; halo, such as chloro, fluoro and the like; and alkoxy having 1 to 5 carbon atoms, for example, methoxy, ethoxy, propoxy, ~nd the like.
It is noted that some of the hole-transporting compound6, as well as some of the electron-transporting ~Z136~Z
-12~
compounds, of the invention have the additional property of be~ng thin-film-forming compounds. As used herein, a compound i~ "thin-film-forming" if, when the material i8 applied by itself to a support such as an electrode, in a thickness no greater than 0.5~, it forms a layer that is substantially free of pinhole6. Reference to compound bPing th~n-film-forming does not necessarily mean, however, that no more than 0.5~ ~ pre~ent. ~he property of thin-film-form~ng ~ 8 useful in that binders can be omitted in both of the layers, if one of the layers of the active zone~ compr~ses such a thin-film-forming compound. Alternatively, a binder which does not otherwi~e hinder the light-producing recom-bination of holes and electrons, i8 hl~O useful in the invention.
Useful examples of compounds capable of forming thin films as defined are set forth hereinafter. Par-ticularly useful examples include compounds containing either a heterocyclic or carbocyclic nucleus and at least two aliphatic chain6 of 3 or more carbon atoms, or at least two moietie6 each of which i6 a) rotatable about a single bond and b) contains at least three aromatic or saturated carbocyclic rings.
For example, hole-transporting compounds that 25 are thin-film-forming include those having the ~tructure a) \ G
w~erein Ql and Q2 are individually moietie~ con-tainlng nitrogen and at least 3 carbocyclic rings at least one of which is aromatic, for example, phenyl.
The carbocyclic r~ngs can be saturated rings, for example, cyclohexyl and cycloheptyl; and G is a linking group such a~ cycloalkylene, e.g., cyclohexylene;
35 arylene 6uch as phenylene; alkylene, such a6 methylene, ethylene, propylene and the like; or a carbon-to-carbon bond. Specific individual examples within structure a) ' ;
~2136~;Z
include l,l-bis(4-di-p-tolylaminophenyl)-4-phenyl-cyclohexane having the Rtructure CH3 CH, .~
J ll 1 U
i) CH3~ -N-~ - N-~ H~
i~S~i .~ \.
1,1-bis(4-di-p-tolylaminophenyl)cyclohexane; and com-15 pound6 having the structure ~ > N~ N \ ~ ~
J~ ,il 1~ /U
wherein n is an integer of from 2 to 4, e.g.~ 4,4 " '-bis(diphenylamino)quadriphenyl.
Still other hole-transporting compounds con-templated a8 being useful include those li6ted in U.S.
Patent No. 4,175,960, line 13 of column 13 to line 42 of column 14, for example, biQ(4-dimethylamino-2-methyl-phenyl)phenylmethane and N,N,N-tri(p-tolyl)amine.
With respect to the thin-film forming electron-transporting compounds, preferred examples include 30 optical br~ghteners. Most preferred are those optical brighteners having the structural formula R~ .-Y-. ~ ~ t t--R~ or R2_~_3~ ~ R~
-14- ~2136~
wherein Rl, R 2~ R~ and R~ are individually hydrogen; 6~turated aliphatic of from 1 to 10 carbon atoms, for example, propyl, t-butyl, heptyl, and the like; aryl of from 6 to 10 carbon atom6, for example, phenyl and naphthyl; or halo such as chloro, fluoro and the like; or Rl and R2 or R3 and R~ taken together compri~e the atoms necessary to complete a fused aromatic ring optionally bear~ng at least one saturated aliphatic of from 1 to 10 carbon atom~, such as methyl, ethyl, propyl and the like;
R 5 iS a saturated aliphat~c of from 1 to 20 carbon atoms, such as methyl, ethyl, n-eico~yl, and the like; aryl of from 6 to 10 carbon atoms, for example, phenyl and naphthyl; carboxyl; hydrogen; cyano; or halo, for example, chloro, fluoro and the like; provided ths~
in formula b) at least two of R~, R~ and Rs are ~aturated aliphatic of from 3 to 10 carbon atom~, e.g., propyl, butyl, heptyl and the like;
Z is -0-, -NH-, or -S-;
Y is -R6~CH~C ~ 6_ ) , -CH-CH-, ~CH-CH ~ 6~CH-CH~n, ... m ~ - , or \~/ ~S/
m is an integer of from 0 to 4;
n ie 0, 1, 2 or 3;
R6 1B erylene of from 6 to 10 carbon atoms, for example, phenylene and naphthylene; and Z~ and Zll are indiv~dually N or CH. As used herein, "aliphatic" include6 substituted aliphatic as well as unsubstituted aliphatic. The substituents in the case of subst$tuted aliphatic include alkyl of from 1 to 5 c~rbon atoms, for example, methyl, ethyl, propyl and the like; aryl of from 6 to 10 carbon atoms, for example, phenyl and naph~hyl, halo, such as chloro, fluoro and the like; nitro; and slkoxy having 1 to 5 carbon atoms, for example, methoxy, ethoxy, propoxy, and the like.
Specific preferred examples of optical brighteners include 2,5-bis(5,7-di-t-pentyl-2-benzoxa-zolyl)-1,3,4-thiadiazole; 4,4'-bls(5,7-di-t-pentyl-2-benzoxazolyl)6tilbene; 2,5-bis(5,7-di-t-phenyl-2-benzoxazolyl)thiophene; 2 9 2'-(p-phenylenedivinylene)bis-benzothiazole; 4,4'-bi6(2-benzoxazolyl)biphenyl; 2,5-bls[5-(~ dimethylbenzyl)-2-benzoxazolyl]thio-phene; 4,4'-bis[5,7-di-(2-methyl-2-butyl)-2-benzoxazolyl]-~tilbene; and 2,5-bis[5,7-di-(2-methyl-2-butyl)-2-benzoxazolyll-3,4-diphenylthiophene.
Still other optical brighteners that are contemplated to be useful are listed in Vol. 5 of Chemistry of Synthetic Dyes, 1971, pages 628-637 and 640. Those that are not already thin-film-forming can be rendered BO by attaching an aliphatic moiety to one or both end rings. Such additional, useful opticsl brighteners include, for example, -CH-CH--~
H H named 5 2-{2-t4-(2-benzimidazolyl)phenyl]vinyl}benzimidazole, CH3\ ~ CH~
~ -CH~CH--~ J~ ll named 5-methyl-2-~2-t4-(5-methyl-2-benzoxszolyl)phenyl] 0 vinyl}benzoxazole, i-CH, ~-~ b~ `S ~ - named 2,5-bis(5-methyl-2-benzoxazolyl)thiophene, lZi3662 ~ CH-CH--~ CO2H named 2-[2-(4-carboxyphenyl)vinyl]benzimidazole, and .~-\.
~ -CH~CH--~ ~--Cl named 1~ 2-[2-(4-chlorophenyl)vinyl~naphth[1,2-d~oxazole.
Still other useful thin-film-forming electron transporting compounds include metal eo~plexe~ of 8-hydroxyquinolineS where the metal is Zn, Al, Mg, or Li.
If one of the active layers 1~ thin-film-forming, then, a6 will be readily apparent, the otherneed not be thin-film-forming as pinholing will not short out the device. For example, a useful device comprises the hole-in~ecting layer compri6ing a thin-film-forming compound as described above, and the lum-inescent layer consisting of a compound that i6 notthin-film-forming, for example, 1,1,4,4-tetraphenyl-1,3-butadiene.
As is apparent from Table I above, useful anode electrodes include coated glass anodes available from PPG Indugtries under the trademark "Nesatron" and useful cathode electrodes include ind~um. Any conventional anode and cathode electrode i8 useful if it has the proper work-function value. For example, the anode should have a high work-function. Other useful anode examples include glass coated with any semitransparent high work-function conductive material, e.g., indium tin oxide, tln oxideJ nickel, or gold. Preferably, such anode electrodes have ~ sheet resistance of about 10 to 1000 ohms/square und an optical transmittance of about 80% for w~velength6 longer than 400 nm. Such high optical transm~ttance, when comb~ned with the hole--17- 12136~z transporting compound's tran~mlttance of at least 90%, insures the s~perior power conversion efficiencies that are characteristic of device~ made in accordance with the present invention.
S Other useful cathode example~ include other metals having a low work-functioD, such a~ silver, tin, lead, magnesium, mangane6e, aluminum and the like, whether or not the metal has high transmittance to the luminescence generated by the device.
Fig. 1 illu~trates an electroluminescent device 10 prepared in accordance with the invention. ~t compri6es an anode electrode 12 comprising a glas~
support 14 coated with a semitranspsrent coating 16 of indium tin oxide on which i~ disposed a hole-in~ecting layer 18. A luminescent layer 20 i8 di6po6ed on layer 18, one or both layers 18 and 20 compri6ing a thin-film-forming compound. Cathode 22 iB disposed on layer 20, and lead wires 24 connect the device to a power ~ource 26. When 60urce 26 i6 turned on, hole6 generated 20 at anode 12 are trsnsported to the interface between layers 18 and 20 where they combine with electron6 transported from cathode 22, generating vi6ible radia-tion h~.
When source 26 i8 operated at a maximum power-25 point voltage of the device 10, e.g., between 15 and 25volts, the maximum power conver6ion efficiency is at least 9 X 10-5 w/w. In some cases thi6 efficiency has been found to be as high as 2 X 10-l. As a re6ult of the improved power conversion efficiencies, the devices 30 of the invention have been found to produce maximum brightnesses as high as 1700 cd¦m2 (500 ft-lamberts).
The EL device of the invention i6 constructed using conventional processes. That i6, each of the hole-in~ecting layer, the luminescent layer and cathode ie applied via 601ution coating or evaporation, with the hole-in~ecting layer preferably being formed fir6t. If the u6eful solvent6 for the lumine6cent layer are al60 ;
12136~;2 good 601vents for the hole-in~ecting layer, then evapo-rat~on iæ preferred for the formation of the lumineæcent layer. A6 used herein, "evaporation" includes all forms of depo6itio~ from the vapor phase, incluting those done under vacuum.
Examples The following examples further illu~trate the inven~ion. In theæe example~, the maximum brightness i~
measured at a voltage ~ust short of that which produce~
irreversible breakdown. It is for this reason that ~ome examples state a voltage for such brightness that exceeds the preferred 25 v limit on the driving voltage.
Example 1 An electroluminescent device, hereinafter, "cell", similar to that of Fig. 1 was prepared as follows:
1) To form the anode electrode, Ne6atron~
glass was first polished with 0.05~ alumina abrasive for a few minutes, followed by ultra~onic cleaning in a 1:1 ~v) mixture of isopropyl alcohol and distilled water. It was then rinsed wlth isopropyl alcohol and blown dry with nitrogen. Finally, it W~8 ultrasonically cleaned in toluene and blown dry with nitrogen before use.
2) 1,1-Bis(4-di-p-tolylaminophenyl)cyclohexane (HI-l) was deposited on the Nesatron~ glass uslng conventional vacuum-deposition techniques: The material was evaporated from an electrically-heated tantalum boat at a temperature of approximately 320C, and at a system pressure of about 5 X 10-5 torr. The thick~ess of the re~ulting HI-l film which was deposited on the Neæatron~ glaææ was about 750A.
However, because of their greater thickness, the voltage required to drive ~uch devices i~ quite high (~ 100 ~5 Vol~s).
In order to reduce the driving voltage to no more than about 25 volts, thin-film electroluminescent device6 are desirable, which as used herein means a device wherein the thickne~s of the active zones or layers, that i8 ~ the material between the electrodes, does not exceed about 1 micron. The thin film format has been particularly difficult to achleve ln light of a pinholing problem. Pinholes are unacceptable because they 6hort out the cell-- see e.g., Dresner, RCA Review, Vol. 30, p. 322ff (June 1969), and especially p. 326.
To prevent formation of pinholes, a binder has been ,~.
conventionally used in the coating formulations.
Example6 of such binderR include add$tion polymers ~uch as polystyrene, and condensation polymers such as polyesters. Although shorting of the cell may be avoided, the use of a binder i8 sometimes unsatisfactory. It require~ the use of solvent coating manufacturing techniques, and the solvent of the one layer may also act a~ a solvent for the underlayer, thu~
preventing a sharp demarcation between layer~. Although one could imagine a process of solvent-coating the one layer that needs a binder and then vapor depositing the layer(s) not needing a binder, a reverse sequence in which the luminescent layer i~ solvent-coated has not proven to be practical when the solvent affects the lower layer.
The cells de6cr~bed in commonly owned U.S.
Application Serial No. 169,705, filed on July 17, 1980, by C. W. Tang entitled "~rganic Electroluminescent Cell", now U.S. Patent No. 4,356,429, are examples of markedly improved devices of the thin film format. Such cell6 have improved power conversion efficiencies by reason of reduced thicknes6 of the luminescent zone, and of the use of an ad~acent hole-in~ecting zone.
Although the cells of the aforesaid application have demonstrated the noted marked improvement over prior art cells, they have not achieved the levels of power conver~ion efficiencies that have been desired, that i~, at least 9 X 10-5 w/w or higher when using a driving voltage no greater than 25 volts. The por-phyrinic compounds in the hole-in~ecting layer are colored and thus tend to undesirably absorb some of the light th~t is emitted by the cell. Also, the por-phyrinic compounds appear to interfere with the efficient radiative recombination of holes and electrons needed to efficiently generate light output.
12136~2 Thus, what ha6 been needed prior to thi6 invention is an electroluminescent, hereinafter, "ELI', device that has power conver~ion efficiencie~ improved by at least one order of magnitude, i.e., to at least 9 X 10-5 w/w, while maintaining the thin film format and reduced driving voltages.
S~MMARY OF THE INVENTION
In accordance with the present invention there is advantageously featured an organic electroluminescent device that haæ the sought-after improved power conver-~ion efficiency as well a8 a thin film format wherein the combined thickness of the act~ve ~ones doe6 not exceed about 1~.
It i8 another advantageous feature of the invention that the luminescent zone or the hole-in~ecting zone o~ such a device is manufacturable from an electron-transporting compound or from a hole-tran~porting compound, respectively, which in many embodiments of the invention is sccomplished without a binder in the respective zone.
Still another advantageou~ feature of the invention is that compounds hflve been discovered for the hole-in~ecting layer that are subgtantially transparent to the generated radiation.
The aforesaid features of the invention result from the following more specific aspects of the inven-tion: In sccord with one aspect, an electroluminescent deYiCe i6 provided comprising, in sequence, an anod~
electrode, a hole-in~ecting zone, A lumine6cent zone, and a cathode electrode, wherein at least one of the electrodes transm~ts at least 80% of radiation having wsvelengths longer than 400 nm. Thi~ device is improved to have a power conversion efficiency of at least 9 X 10 5 w/w and said zones have a combined thickness of no greater than about 1 micron.
Most preferably, the luminescent zone of the afore~a~d device comprises a electron-transporting ;
4 lZ~;~662 compound that provideæ an electroluminescent quantum efficiency of at least about 5 X 10-~ pho-tons/electron, when used in a teæt device driven at no more than the le6ser of i) 25 volts snd ii) the voltage which produces the maximum power conver~ion efficiency of ~aid device, the test device comprising 1) a hole-in~ecting zone consi~ting essentially of l,l-bi6(4-di-p-tolylaminophenyl~cyclohexane, such hole-in3ecting zone and ~aid luminescent zone hav~ng a combined 10 thicknes~ of no more than 1~, 2~ an anode electrode $hat transmits at least 80a of radiation having wavelengths longer than 400 nm, and 3) an indium cathode.
Other advantageous features of the invention will become apparent upon reference to the following Description of the Preferred Embodimen~s when read in light of the attached drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a partially schematic section view of a device of the invention connected to a power source;
20 and Fig. 2 iB a log-log graph of power convergion efficiences vs. electroluminescent quantum efficiencies for devices produced in accordance with the invention.
DESCRIPTION OF THE PREFERRED EMBODIMEWTS
This invention i8 described particularly in connection with embodiments wherein the materials of the electroluminescent device are in layers or laminae, one on top of the other. In addition, the invention is applicable to an electroluminescent (hereinafter, "EL") cell or device wherein the hole-transporting material and the luminescent material are in zones, whether the zones are in layers or otherwise.
The device of this invention compri6es a hole-in3ecting layer and a luminescent layer. ~he 35 hole-in3ecting layer comprises a hole-transporting compound, while the luminescent layer comprises an electron-tran6porting compound.
~2136~2 We have discovered that there are certain electron-transporting compounds that produce EL quantum efficiency values in exces~ of 5 X 10-~ pho-tons/electron, when u~ed in a cell driven and con6tructed ~s herein~fter described. Because of the direct relationship which occurs between power conver-sion efficiencies and EL quantum efficiencie6, these compounds insure that for the drivlng vol~age noted, the power conver~ion efficiency will be at least 9 X 10-5 w/w. Because these compounds are readily deposited in a thin film format, a thin-film device i8 readily obtain-able wherein the combined thickness of the active zones doe6 not exceed 1~.
As u6ed herein, an electron-tran6porting com-pound i6 a compound that i8 reducible in an oxidation-reduction reaction. It is tho~e electron-transporting compounds producing at least 5 X 10-~ EL quantum efficiency, a6 per the te6t hereinafter defined, that are parti~ularly useful in thi6 invention. (As is well known, the EL quantum efficiency simply equals the ratio of photon6 per second emitted from the cell, to the electrons per second measured in the external circuit.
This efficiency is not to be confused with power conversion efficiency, which is defined in units of watt/watt.) To determine whether an electron-transporting compound produces an EL quantum efficiency at least equal to 5 X 10-~ photons/electron (or O.OSa), the following test i6 conducted:
An EL cell i8 constructed in the following ~equence: an anode electrode that transmits at least 80% of radiation having wavelengths longer than 400 nm, a hole-in~ecting layer consisting essentially of 1,1-bis(4-di-p-tolylaminophenyl)cyclohexane, a layer of the electron-transporting compound in question, a~d an indium cathode, wherein the hole-in~ecting layer and the -6- 1 Z ~ 3 6 ~ Z
luminescent l~yer together do not exceed 1~ in thick-ness. A driving voltage i~ spplied, and iB increa6ed until either the maximum power conversion efficiency, or 25 volts, is reached, whichever occurs first. The maximum EL quantum efficiency i~ measured at thi6 voltage.
Table I illustrates the EL quantum efficiencies for 60me u6eful electron-transporting compounds, when tested in the device constructed aR noted and driven at the noted voltage6. For each of these examples, the voltage of the maximum EL quantum efficiency was less than the 25-volt limit.
-7- ~ Z1366Z
~ ~o c C
? JJ Cg C u~
)~ o C o oo Q
~t ~ P1 ~ ~
e ~ ~ o , eO ~ o o o o o o o lU
E o~
X ~ ~ ~ ~ ~ K U~ X
C~ ~ ~ X
~ q~
E~
~ 04 D O' V
D 1~ C
C ~ ~ ~
o ~ o o o o o o , O `~
C ~
o ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ C
.C ~ ~ _ O :C CO ~ ~ ~ ~ o X .~CO
v Q~ o c~ a 0 ~ ~ ~ ~ v ~0 ~: ~ C ~ C ~ C t~ C ~ g ~ ~
C ~ C ~ ~ ~ C ~ C ~ C ~ C ~
JJ _ ~ 1~ l H 1-1 O
~ g ~ ~ o ~ eO ~ eO ~ g ¢ eO ¢ 8 ~ 80 ~ ~
M ~ C ' E3 ~ 3 ~ O ~I O ~I O ~-I O ~ O ~ O ~
~ ~ ~ ~ v ~ J~ n v u~ J~ Lr, J~ v u~ e 4~ ~ _1 x ~ ~ 3 O ~ ~ _ Z :Z Z Z Z Z :~ Z ~lt -8~ 13~6Z
V' X ~
i \ ~ ~ ~
// tD
0 ~
~ ~ o _~ N
t) 0 / ~ O
N
C
.C
O
C
/ _l .=. ~ ~ I I
O =- ~ O ~//
= V
_ Z/ ~-= O .,~ // \ ~ ~
=- ~ Z;D 5 El o--- 0 ~ --~
O ~
_1 ~ 0 P
_I ~ I
1213~62 ~C
_, .~, _, ._ .=.
:~ o o ;\ /;
o;\ /; N
~ =- C.~ :C U ; ~ \ f ) N E3 -- IZ~ / N I S w C
Z ~ I G / ~ O
r~ ~ ; . c . ~Y ~ \/~
C
.=. , ~ . ~ ~ ~ o ~ . C
.=. ~ ~ // ~ .c o . - . ~ 0 ~: 0 .D C~
~ ~ w -lo- lZ1366Z
/ ~ ~U ~
.
_~ ~ N
~; ~ N ~ ~ X X
N =. X ~3 C
Z~ f ~ ~
.=. :>~ ;=. 1 ,D
~ =- U~ ,~
=- V / \ /
=- ~
0 C~ ~ 0 o `~
~ - ~ 0 ~
Hole-transporting compound6 of the hole-in3ecting layer, as used herein, Are compounds which, when disposed between two electrode6 to which a field is applied, and a hole is in~ected from the anode, S permit adequate transport of holes to the cathode electrode. More ~pecifically, a compound i~ defined to be hole-transporting if it ha6 a hole mobility factor of at least 10-6 cm2/volt-sec when a layer i8 dispo~ed between electrodes to which an electric field of 10 to 10 6 volt6/cm is applied. It ha6 been found thst the most preferred hole-transporting compounds are aromatic amine~ that are readily and rever6ibly cxidiz-able~
Mo~t preferably, the hole-in~ecting layer i8 the trsnsparent portion of the active layers, becau6e i~
is ad~acent to the transparent electrode. Thus, the hole-transporting compound is al60 preferably at least 90% transmissive at 400 nm, or longer, wavelengths.
That iB, the hole-transporting compound is preferably essentially colorless.
Preferred examples of useful hole-transporting compound R that have the afore-noted light transmittance include amines that are solid at room temperature and in which at least one nitrogen atom is tri-~ubstituted with substituents at least one of which is aryl. As will be apparent from the examples that follow, "aryl" sub-stituents in hole-transporting compounds includes substituted aryl as well as unsubstituted aryl, such as phenyl and methylphenyl. Examples of u~eful substi-tuents include alkyl of 1 to 5 carbon atoms, for exam-ple, methyl, ethyl, propyl, and the like; halo, such as chloro, fluoro and the like; and alkoxy having 1 to 5 carbon atoms, for example, methoxy, ethoxy, propoxy, ~nd the like.
It is noted that some of the hole-transporting compound6, as well as some of the electron-transporting ~Z136~Z
-12~
compounds, of the invention have the additional property of be~ng thin-film-forming compounds. As used herein, a compound i~ "thin-film-forming" if, when the material i8 applied by itself to a support such as an electrode, in a thickness no greater than 0.5~, it forms a layer that is substantially free of pinhole6. Reference to compound bPing th~n-film-forming does not necessarily mean, however, that no more than 0.5~ ~ pre~ent. ~he property of thin-film-form~ng ~ 8 useful in that binders can be omitted in both of the layers, if one of the layers of the active zone~ compr~ses such a thin-film-forming compound. Alternatively, a binder which does not otherwi~e hinder the light-producing recom-bination of holes and electrons, i8 hl~O useful in the invention.
Useful examples of compounds capable of forming thin films as defined are set forth hereinafter. Par-ticularly useful examples include compounds containing either a heterocyclic or carbocyclic nucleus and at least two aliphatic chain6 of 3 or more carbon atoms, or at least two moietie6 each of which i6 a) rotatable about a single bond and b) contains at least three aromatic or saturated carbocyclic rings.
For example, hole-transporting compounds that 25 are thin-film-forming include those having the ~tructure a) \ G
w~erein Ql and Q2 are individually moietie~ con-tainlng nitrogen and at least 3 carbocyclic rings at least one of which is aromatic, for example, phenyl.
The carbocyclic r~ngs can be saturated rings, for example, cyclohexyl and cycloheptyl; and G is a linking group such a~ cycloalkylene, e.g., cyclohexylene;
35 arylene 6uch as phenylene; alkylene, such a6 methylene, ethylene, propylene and the like; or a carbon-to-carbon bond. Specific individual examples within structure a) ' ;
~2136~;Z
include l,l-bis(4-di-p-tolylaminophenyl)-4-phenyl-cyclohexane having the Rtructure CH3 CH, .~
J ll 1 U
i) CH3~ -N-~ - N-~ H~
i~S~i .~ \.
1,1-bis(4-di-p-tolylaminophenyl)cyclohexane; and com-15 pound6 having the structure ~ > N~ N \ ~ ~
J~ ,il 1~ /U
wherein n is an integer of from 2 to 4, e.g.~ 4,4 " '-bis(diphenylamino)quadriphenyl.
Still other hole-transporting compounds con-templated a8 being useful include those li6ted in U.S.
Patent No. 4,175,960, line 13 of column 13 to line 42 of column 14, for example, biQ(4-dimethylamino-2-methyl-phenyl)phenylmethane and N,N,N-tri(p-tolyl)amine.
With respect to the thin-film forming electron-transporting compounds, preferred examples include 30 optical br~ghteners. Most preferred are those optical brighteners having the structural formula R~ .-Y-. ~ ~ t t--R~ or R2_~_3~ ~ R~
-14- ~2136~
wherein Rl, R 2~ R~ and R~ are individually hydrogen; 6~turated aliphatic of from 1 to 10 carbon atoms, for example, propyl, t-butyl, heptyl, and the like; aryl of from 6 to 10 carbon atom6, for example, phenyl and naphthyl; or halo such as chloro, fluoro and the like; or Rl and R2 or R3 and R~ taken together compri~e the atoms necessary to complete a fused aromatic ring optionally bear~ng at least one saturated aliphatic of from 1 to 10 carbon atom~, such as methyl, ethyl, propyl and the like;
R 5 iS a saturated aliphat~c of from 1 to 20 carbon atoms, such as methyl, ethyl, n-eico~yl, and the like; aryl of from 6 to 10 carbon atoms, for example, phenyl and naphthyl; carboxyl; hydrogen; cyano; or halo, for example, chloro, fluoro and the like; provided ths~
in formula b) at least two of R~, R~ and Rs are ~aturated aliphatic of from 3 to 10 carbon atom~, e.g., propyl, butyl, heptyl and the like;
Z is -0-, -NH-, or -S-;
Y is -R6~CH~C ~ 6_ ) , -CH-CH-, ~CH-CH ~ 6~CH-CH~n, ... m ~ - , or \~/ ~S/
m is an integer of from 0 to 4;
n ie 0, 1, 2 or 3;
R6 1B erylene of from 6 to 10 carbon atoms, for example, phenylene and naphthylene; and Z~ and Zll are indiv~dually N or CH. As used herein, "aliphatic" include6 substituted aliphatic as well as unsubstituted aliphatic. The substituents in the case of subst$tuted aliphatic include alkyl of from 1 to 5 c~rbon atoms, for example, methyl, ethyl, propyl and the like; aryl of from 6 to 10 carbon atoms, for example, phenyl and naph~hyl, halo, such as chloro, fluoro and the like; nitro; and slkoxy having 1 to 5 carbon atoms, for example, methoxy, ethoxy, propoxy, and the like.
Specific preferred examples of optical brighteners include 2,5-bis(5,7-di-t-pentyl-2-benzoxa-zolyl)-1,3,4-thiadiazole; 4,4'-bls(5,7-di-t-pentyl-2-benzoxazolyl)6tilbene; 2,5-bis(5,7-di-t-phenyl-2-benzoxazolyl)thiophene; 2 9 2'-(p-phenylenedivinylene)bis-benzothiazole; 4,4'-bi6(2-benzoxazolyl)biphenyl; 2,5-bls[5-(~ dimethylbenzyl)-2-benzoxazolyl]thio-phene; 4,4'-bis[5,7-di-(2-methyl-2-butyl)-2-benzoxazolyl]-~tilbene; and 2,5-bis[5,7-di-(2-methyl-2-butyl)-2-benzoxazolyll-3,4-diphenylthiophene.
Still other optical brighteners that are contemplated to be useful are listed in Vol. 5 of Chemistry of Synthetic Dyes, 1971, pages 628-637 and 640. Those that are not already thin-film-forming can be rendered BO by attaching an aliphatic moiety to one or both end rings. Such additional, useful opticsl brighteners include, for example, -CH-CH--~
H H named 5 2-{2-t4-(2-benzimidazolyl)phenyl]vinyl}benzimidazole, CH3\ ~ CH~
~ -CH~CH--~ J~ ll named 5-methyl-2-~2-t4-(5-methyl-2-benzoxszolyl)phenyl] 0 vinyl}benzoxazole, i-CH, ~-~ b~ `S ~ - named 2,5-bis(5-methyl-2-benzoxazolyl)thiophene, lZi3662 ~ CH-CH--~ CO2H named 2-[2-(4-carboxyphenyl)vinyl]benzimidazole, and .~-\.
~ -CH~CH--~ ~--Cl named 1~ 2-[2-(4-chlorophenyl)vinyl~naphth[1,2-d~oxazole.
Still other useful thin-film-forming electron transporting compounds include metal eo~plexe~ of 8-hydroxyquinolineS where the metal is Zn, Al, Mg, or Li.
If one of the active layers 1~ thin-film-forming, then, a6 will be readily apparent, the otherneed not be thin-film-forming as pinholing will not short out the device. For example, a useful device comprises the hole-in~ecting layer compri6ing a thin-film-forming compound as described above, and the lum-inescent layer consisting of a compound that i6 notthin-film-forming, for example, 1,1,4,4-tetraphenyl-1,3-butadiene.
As is apparent from Table I above, useful anode electrodes include coated glass anodes available from PPG Indugtries under the trademark "Nesatron" and useful cathode electrodes include ind~um. Any conventional anode and cathode electrode i8 useful if it has the proper work-function value. For example, the anode should have a high work-function. Other useful anode examples include glass coated with any semitransparent high work-function conductive material, e.g., indium tin oxide, tln oxideJ nickel, or gold. Preferably, such anode electrodes have ~ sheet resistance of about 10 to 1000 ohms/square und an optical transmittance of about 80% for w~velength6 longer than 400 nm. Such high optical transm~ttance, when comb~ned with the hole--17- 12136~z transporting compound's tran~mlttance of at least 90%, insures the s~perior power conversion efficiencies that are characteristic of device~ made in accordance with the present invention.
S Other useful cathode example~ include other metals having a low work-functioD, such a~ silver, tin, lead, magnesium, mangane6e, aluminum and the like, whether or not the metal has high transmittance to the luminescence generated by the device.
Fig. 1 illu~trates an electroluminescent device 10 prepared in accordance with the invention. ~t compri6es an anode electrode 12 comprising a glas~
support 14 coated with a semitranspsrent coating 16 of indium tin oxide on which i~ disposed a hole-in~ecting layer 18. A luminescent layer 20 i8 di6po6ed on layer 18, one or both layers 18 and 20 compri6ing a thin-film-forming compound. Cathode 22 iB disposed on layer 20, and lead wires 24 connect the device to a power ~ource 26. When 60urce 26 i6 turned on, hole6 generated 20 at anode 12 are trsnsported to the interface between layers 18 and 20 where they combine with electron6 transported from cathode 22, generating vi6ible radia-tion h~.
When source 26 i8 operated at a maximum power-25 point voltage of the device 10, e.g., between 15 and 25volts, the maximum power conver6ion efficiency is at least 9 X 10-5 w/w. In some cases thi6 efficiency has been found to be as high as 2 X 10-l. As a re6ult of the improved power conversion efficiencies, the devices 30 of the invention have been found to produce maximum brightnesses as high as 1700 cd¦m2 (500 ft-lamberts).
The EL device of the invention i6 constructed using conventional processes. That i6, each of the hole-in~ecting layer, the luminescent layer and cathode ie applied via 601ution coating or evaporation, with the hole-in~ecting layer preferably being formed fir6t. If the u6eful solvent6 for the lumine6cent layer are al60 ;
12136~;2 good 601vents for the hole-in~ecting layer, then evapo-rat~on iæ preferred for the formation of the lumineæcent layer. A6 used herein, "evaporation" includes all forms of depo6itio~ from the vapor phase, incluting those done under vacuum.
Examples The following examples further illu~trate the inven~ion. In theæe example~, the maximum brightness i~
measured at a voltage ~ust short of that which produce~
irreversible breakdown. It is for this reason that ~ome examples state a voltage for such brightness that exceeds the preferred 25 v limit on the driving voltage.
Example 1 An electroluminescent device, hereinafter, "cell", similar to that of Fig. 1 was prepared as follows:
1) To form the anode electrode, Ne6atron~
glass was first polished with 0.05~ alumina abrasive for a few minutes, followed by ultra~onic cleaning in a 1:1 ~v) mixture of isopropyl alcohol and distilled water. It was then rinsed wlth isopropyl alcohol and blown dry with nitrogen. Finally, it W~8 ultrasonically cleaned in toluene and blown dry with nitrogen before use.
2) 1,1-Bis(4-di-p-tolylaminophenyl)cyclohexane (HI-l) was deposited on the Nesatron~ glass uslng conventional vacuum-deposition techniques: The material was evaporated from an electrically-heated tantalum boat at a temperature of approximately 320C, and at a system pressure of about 5 X 10-5 torr. The thick~ess of the re~ulting HI-l film which was deposited on the Neæatron~ glaææ was about 750A.
3) 4,4'-Bis(5,7-di-t-pentyl-2-benzoxazolyl)-stilbene (El) was then deposited on top of the HI-l layer using the same techniques described in (2), but employing a source temperature of about 350C. The thicknes~ of the El layer waæ al~o about 750A.
4) Indium was then deposited on top of the El film through a 6hadow mask. The area of the In electrode was 0-1 cm2, which a1BO defined the active area of the electrolumlnescent cell.
The completed cell emitted blue-green light when bia~ed with the Nesatron~ glas~ electrode positive. The emitted light had a maximum emission at 520 nm. The maximum brightness achieved was 340 cd/m2 at a current density of about 140 mA/cm2 when the applied voltage was 22 volts. The maximum power conver~ion efficiency was about 1.4 X 10-~ w/w and the maximum electroluminescent quantum efficiency was about 1.2 X 10-2 photons/electron when driven at 20 volts.
Example 2 - Use of Hole-In~ecting Layer That Is Not Thin-Film-Forming An electroluminescent cell wa6 prepared a8 described in Example 1, except that N,N,N-tri(p-tolyl)amine was used as the hole-in~ecting layer in place of HI-l. This am~ne compound has the structure !
~t ll 1 !1 CH~ . ~ 3 The cell was prepared in the same manner as described for Example 1, except that the source tempera-ture for the amlne evaporation was 120~C. The thickness was about 750A. Upon application of 30 volts to this cell, a current density of sbout 40 mA/cm2 and a maximum br~ghtne~s of 102 cd/m2 was obtained. The emitted light was sgain blue-green, with the maxi~um ~Z136~2 emission at 520 nm. The maximum power conversion efficiency was 8.1 X 10-~ w/w and the maximum EL
quantum efficiency was 6.9 X 10-~ photons/electron when driven at 20 vo~t6.
The6e result~ demonstr~ted that if the lumines-cent layer wa~ free of pinhole~ becsu6e it comprised a thin-film-forming compound, then the hole-in~ecting layer did not have to be a thin-film-formlng compound nor contain a binder.
ExamPle 3 - Alternate Materials for Lumine6cent Layer An electroluminescent cell was prepared as in Example 1, except thst the following optical brightener was u~ed a~ the lumine~cent layer:
C2Hs C2Hs (CH3)2C\i~ N~ C(CH~)2 C2Hs~C(CH3)2 C2Hs~C(CH~) 2 [2,5-bi6(5,7-di-t-pentyl-2-benzoxazolyl)-1,3-thiadiszole].
The cell was prepared in the 6ame manner de~cribed for Example 1, except that the ~ource tempera-ture for evaporstion of the optical brightener was 260~C. The emitted light was orange, with the maximum emis6ion at 590 nm. The maximum brigh~ness obtsined wss about 340 cd/m2 at 30 volt6 and 40 mA/cm2. The maximum power conversion efficiency wa6 1.5 X 10-~ w/w and the maximum EL quantum efficlency was 1.4 X 10-2 3Q photon~/electron when driven at 20 volts.
Example 4 - Alternate Material6 for Luminescent Layer An electroluminescent cell was prepared as in Example 1 above except that 2,2'-(p-phenylenedi-vinylene)bi~benzothiazole (E3) wa~ used as the lumines-cent layer and was evaporated at 300UC
1213~6Z
-CH~CH--~ ~--CH-CH-~
The cell, Nesatron~/HI-l/E3/In, emltted green light with maximum emission at 560 nm. The maximum brightness obtained WM6 340 cd/m2 at 17.5 volt6 and 200 mA/cm2. The maximum power conver~ion effieieney was 4 X 10-~ w/w, and the maximum electrolumine~cent quantum effioiency was 3 X 10-3 photons/electron when driven at 15 volt6.
Example 5 - Alternate Materials for Luminescent Layer An electroluminescent cell wa~ prepared a~
described in Example 1 above, except that 2-(4-bi-phenylyl)-6-phenylbenzoxazole (PBB0) wa~ used a8 the luminescent layer, instead of El, and wa~ evaporated at 200~C.
~ b / ~ ~
The cell, Ne~atron~/HI-l/PBB0/In, emitted whit~sh-blue ligh~. The maximum brightness obtained was about 34 cd/m2 at 25 volts and 50mA/cm2. The maximum power conversion efficiency was 9.5 X 10-5 w/w~ and the maximum electroluminescent quantum effi-ciency w~s 8 X ~0~~ photons/electron when driven at 20 volts.
Exam~les 6 and 7 - Alternate Materials for Luminescent Layer An electroluminescent cell wa~ prepared as described for Example 1, except that the luminescent layer comprised 2,5-bie[5-(a,~-dimethylbenzyl)-~-benzoxazolyl]-thiophene (Ex. 6), and 2,5-bisl5,7-d$-(2-methyl-2-butyl)-2-benzoxazolyl~-3,4-diphenyl-thlophene (Ex. 7), ~nstead of El, evaporated at a temperature of 340C. Table II ~ets forth the results.
lZ13662 -22_ J-C C
u~
t~ ~ 0 ~
æ ~ ~
c ~ _ e o _ c a~ ~ 0 o ~ o~ O
~ ~ o g )~ ~C O
X 0 ~ ~C o ~ ~ o 0 ~ ~ 4
The completed cell emitted blue-green light when bia~ed with the Nesatron~ glas~ electrode positive. The emitted light had a maximum emission at 520 nm. The maximum brightness achieved was 340 cd/m2 at a current density of about 140 mA/cm2 when the applied voltage was 22 volts. The maximum power conver~ion efficiency was about 1.4 X 10-~ w/w and the maximum electroluminescent quantum efficiency was about 1.2 X 10-2 photons/electron when driven at 20 volts.
Example 2 - Use of Hole-In~ecting Layer That Is Not Thin-Film-Forming An electroluminescent cell wa6 prepared a8 described in Example 1, except that N,N,N-tri(p-tolyl)amine was used as the hole-in~ecting layer in place of HI-l. This am~ne compound has the structure !
~t ll 1 !1 CH~ . ~ 3 The cell was prepared in the same manner as described for Example 1, except that the source tempera-ture for the amlne evaporation was 120~C. The thickness was about 750A. Upon application of 30 volts to this cell, a current density of sbout 40 mA/cm2 and a maximum br~ghtne~s of 102 cd/m2 was obtained. The emitted light was sgain blue-green, with the maxi~um ~Z136~2 emission at 520 nm. The maximum power conversion efficiency was 8.1 X 10-~ w/w and the maximum EL
quantum efficiency was 6.9 X 10-~ photons/electron when driven at 20 vo~t6.
The6e result~ demonstr~ted that if the lumines-cent layer wa~ free of pinhole~ becsu6e it comprised a thin-film-forming compound, then the hole-in~ecting layer did not have to be a thin-film-formlng compound nor contain a binder.
ExamPle 3 - Alternate Materials for Lumine6cent Layer An electroluminescent cell was prepared as in Example 1, except thst the following optical brightener was u~ed a~ the lumine~cent layer:
C2Hs C2Hs (CH3)2C\i~ N~ C(CH~)2 C2Hs~C(CH3)2 C2Hs~C(CH~) 2 [2,5-bi6(5,7-di-t-pentyl-2-benzoxazolyl)-1,3-thiadiszole].
The cell was prepared in the 6ame manner de~cribed for Example 1, except that the ~ource tempera-ture for evaporstion of the optical brightener was 260~C. The emitted light was orange, with the maximum emis6ion at 590 nm. The maximum brigh~ness obtsined wss about 340 cd/m2 at 30 volt6 and 40 mA/cm2. The maximum power conversion efficiency wa6 1.5 X 10-~ w/w and the maximum EL quantum efficlency was 1.4 X 10-2 3Q photon~/electron when driven at 20 volts.
Example 4 - Alternate Material6 for Luminescent Layer An electroluminescent cell was prepared as in Example 1 above except that 2,2'-(p-phenylenedi-vinylene)bi~benzothiazole (E3) wa~ used as the lumines-cent layer and was evaporated at 300UC
1213~6Z
-CH~CH--~ ~--CH-CH-~
The cell, Nesatron~/HI-l/E3/In, emltted green light with maximum emission at 560 nm. The maximum brightness obtained WM6 340 cd/m2 at 17.5 volt6 and 200 mA/cm2. The maximum power conver~ion effieieney was 4 X 10-~ w/w, and the maximum electrolumine~cent quantum effioiency was 3 X 10-3 photons/electron when driven at 15 volt6.
Example 5 - Alternate Materials for Luminescent Layer An electroluminescent cell wa~ prepared a~
described in Example 1 above, except that 2-(4-bi-phenylyl)-6-phenylbenzoxazole (PBB0) wa~ used a8 the luminescent layer, instead of El, and wa~ evaporated at 200~C.
~ b / ~ ~
The cell, Ne~atron~/HI-l/PBB0/In, emitted whit~sh-blue ligh~. The maximum brightness obtained was about 34 cd/m2 at 25 volts and 50mA/cm2. The maximum power conversion efficiency was 9.5 X 10-5 w/w~ and the maximum electroluminescent quantum effi-ciency w~s 8 X ~0~~ photons/electron when driven at 20 volts.
Exam~les 6 and 7 - Alternate Materials for Luminescent Layer An electroluminescent cell wa~ prepared as described for Example 1, except that the luminescent layer comprised 2,5-bie[5-(a,~-dimethylbenzyl)-~-benzoxazolyl]-thiophene (Ex. 6), and 2,5-bisl5,7-d$-(2-methyl-2-butyl)-2-benzoxazolyl~-3,4-diphenyl-thlophene (Ex. 7), ~nstead of El, evaporated at a temperature of 340C. Table II ~ets forth the results.
lZ13662 -22_ J-C C
u~
t~ ~ 0 ~
æ ~ ~
c ~ _ e o _ c a~ ~ 0 o ~ o~ O
~ ~ o g )~ ~C O
X 0 ~ ~C o ~ ~ o 0 ~ ~ 4
5 :~
~ O ~ ,~ o 0 ~ . _~
~ É ~ ~ K 3 ~ ~
0 N ~ ~
v E ~ E E E
X --~ O ~ o O ~ O
O ~ C U) I~ ~ C: o ~
C
~0 a ~ 0 X ~ U
J~ ~1 ~ o xl ~ ~D 1~
Example 8 - E~lectron-Transport~n~ pound_That is Not Th~n-Film-Forming An electroluminescent cell was prepared a8 ~ n Example 1 above except that 1,1,4,4-tetraphenyl-1,3-butadiene (TPB) was u~ed as the lumine6cent layer.
.~-\. .~-\.
C~CH-CH~C~ ,U
¦~ \i!~TPB i i The &ource temperature for the TPB ~ublimation was 210~C. The cell emitted blue light with maximum emis-sion at 450 nm. The maximum brightne6s obtained WR8 about 102 cd/m2 ~t 20 volts and 200 mA/cm2. The maximum power ca~ver6ion efficlency was about 2 X 10-~w/w, and the maximum electroluminescent quantum efficiency w88 1.2 X 10-3 photons/electron when driven at 15 volts. This cell was operatlonal in spite of the non-uniform and non-film-forming nature of the evaporated TPB layer, which hss the appearance of a mosaic of small clusters when viewed under a microscope.
Example& 9 and 10 - Use of Metal Complexes of 8-hydroxyquinoline as the Electron-Tran~porting ComPound An electroluminescent cell was prepared a~ in Example 1, except that bis(8-hydroxyquinolino)aluminum (Ex. 9), and bis(8-hydroxyquinolino)magnesium having the structure Q ~
~g~0 (Ex. 10), ! Y l' ~./ ~./
-24- lZ~366Z
respectively, were used a~ the luminescent layer. The process conditions were as described in Example 1, except that the source temperature for the metal com-plexes was 330C, Ex. 9, and 410~C, Example 10, respec-tively. Table III sets forth the results.
~213G6Z
~ os ~ ~
_, _, ~
E ~ o _ C o _ C
C ~ ~ C ~J ~ C ~
~ O ~ ~ o V
X ~ ) O ~ U~ o a~
~ ~ ~ U~
C ~ ~ ~r O U O O
u K ~
~-~1 x ~ o~ ~
~ L~ ~ ~ E
_l ~ C ~ ~ U ~ _ ~d:~ V " V -- V
E~ ~ ~
K `J o O ~ ~ O
C g _~ ~ to C C
g ~ ~ U~ oO
3 0 ~ _1 ~
S ~
xl o~
?
-26- 12~3~6Z
The efficiencies listed in the aforesaid example6 hsve been plo~ted in Fig. 2 for convenience. The dot~ed l~ne of Fig. 2 is intended only to indicate the trend, ~nd does no~ represent a best fit by any method. The d~ts there~n illustrated i8 approxim~tely linear, in accor-dance with the relationship log (power conversion efficiency) ~ log (EL
quantum efficiency) ~ log K
where K is the intercept value and is a factor con-trolled in part by the driving voltage. A6 the drivingvoltage (source 26 in Fig. 1) goeE up in value, the curve of Fig. 2 shifts downwardly. Thus, at higher driving voltages, the same EL quantum efficiencie~ will tend to no longer produce the desired power conversion 5 efficiency of at least 9 X 10-5 w/w.
The invention hag been tescribed in detail with particular reference to preferred embodiment6 thereof, but it will be understood that variations and modifica-tions can be effected within the spirit and scope of the 0 invention.
~ O ~ ,~ o 0 ~ . _~
~ É ~ ~ K 3 ~ ~
0 N ~ ~
v E ~ E E E
X --~ O ~ o O ~ O
O ~ C U) I~ ~ C: o ~
C
~0 a ~ 0 X ~ U
J~ ~1 ~ o xl ~ ~D 1~
Example 8 - E~lectron-Transport~n~ pound_That is Not Th~n-Film-Forming An electroluminescent cell was prepared a8 ~ n Example 1 above except that 1,1,4,4-tetraphenyl-1,3-butadiene (TPB) was u~ed as the lumine6cent layer.
.~-\. .~-\.
C~CH-CH~C~ ,U
¦~ \i!~TPB i i The &ource temperature for the TPB ~ublimation was 210~C. The cell emitted blue light with maximum emis-sion at 450 nm. The maximum brightne6s obtained WR8 about 102 cd/m2 ~t 20 volts and 200 mA/cm2. The maximum power ca~ver6ion efficlency was about 2 X 10-~w/w, and the maximum electroluminescent quantum efficiency w88 1.2 X 10-3 photons/electron when driven at 15 volts. This cell was operatlonal in spite of the non-uniform and non-film-forming nature of the evaporated TPB layer, which hss the appearance of a mosaic of small clusters when viewed under a microscope.
Example& 9 and 10 - Use of Metal Complexes of 8-hydroxyquinoline as the Electron-Tran~porting ComPound An electroluminescent cell was prepared a~ in Example 1, except that bis(8-hydroxyquinolino)aluminum (Ex. 9), and bis(8-hydroxyquinolino)magnesium having the structure Q ~
~g~0 (Ex. 10), ! Y l' ~./ ~./
-24- lZ~366Z
respectively, were used a~ the luminescent layer. The process conditions were as described in Example 1, except that the source temperature for the metal com-plexes was 330C, Ex. 9, and 410~C, Example 10, respec-tively. Table III sets forth the results.
~213G6Z
~ os ~ ~
_, _, ~
E ~ o _ C o _ C
C ~ ~ C ~J ~ C ~
~ O ~ ~ o V
X ~ ) O ~ U~ o a~
~ ~ ~ U~
C ~ ~ ~r O U O O
u K ~
~-~1 x ~ o~ ~
~ L~ ~ ~ E
_l ~ C ~ ~ U ~ _ ~d:~ V " V -- V
E~ ~ ~
K `J o O ~ ~ O
C g _~ ~ to C C
g ~ ~ U~ oO
3 0 ~ _1 ~
S ~
xl o~
?
-26- 12~3~6Z
The efficiencies listed in the aforesaid example6 hsve been plo~ted in Fig. 2 for convenience. The dot~ed l~ne of Fig. 2 is intended only to indicate the trend, ~nd does no~ represent a best fit by any method. The d~ts there~n illustrated i8 approxim~tely linear, in accor-dance with the relationship log (power conversion efficiency) ~ log (EL
quantum efficiency) ~ log K
where K is the intercept value and is a factor con-trolled in part by the driving voltage. A6 the drivingvoltage (source 26 in Fig. 1) goeE up in value, the curve of Fig. 2 shifts downwardly. Thus, at higher driving voltages, the same EL quantum efficiencie~ will tend to no longer produce the desired power conversion 5 efficiency of at least 9 X 10-5 w/w.
The invention hag been tescribed in detail with particular reference to preferred embodiment6 thereof, but it will be understood that variations and modifica-tions can be effected within the spirit and scope of the 0 invention.
Claims (9)
- WHAT IS CLAIMED IS:
l. In an electroluminescent device compris-ing, in sequence, an anode electrode, a hole-injecting zone, an organic luminescent zone, and a cathode elec-trode, at least one of said electrodes being capable of transmitting at least 80% of radiation having wave-lengths longer than 400 nm, the improvement wherein said luminescent zone comprises an electron-transporting compound that pro-vides a maximum electroluminescent quantum efficiency of at least about 5 X 10-4 photons/electron, when used in a test device driven at no more than the les-ser of (i) 25 volts and (ii) the voltage which pro-duces the maximum power conversion efficiency of said device, said test device comprising (1) a hole-injec-ting zone consisting essentially of 1,1,-bis(4-di-p-tolylaminophenyl)cyclohexane, said hole-injecting zone and said luminescent zone having a combined thickness of no more than 1 micron, (2) an anode electrode that transmits at least 80% of radiation having wavelengths longer than 500 nm, and (3) an indium cathode, and wherein said device has a power conver-stion efficiency of at least 9 X 10-5 w/w and said zones have a combined thickness that is no greater than about 1 micron. - 2. A device as defined in claim 1, wherein said electron-transporting compound is an optical brightener.
- 3. A device as defined in claim 2, wherein said optical brightener has the structural formula a) or b) wherein Rl, R2, R3 and R4 are individually hydrogen; saturated aliphatic of from 1 to 10 carbon atoms, aryl of from 6 to 10 carbon atoms, or halo, or R1 and R2 or R3 and R4 taken together comprise the atoms necessary to complete a fused aromatic ring, R5 is saturated aliphatic of from 1 to 20 carbon atoms, aryl of from 6 to 10 carbon atoms, carboxyl, hydrogen, cyano or halo; provided that in formula b) at least two of R3, R4 and R5 are saturated aliphatic of from 3 to 10 carbon atoms;
Z is -O-, -NH-, or -S-;
Y is -R6?CH?CH?nR6-, m is an integer of from 0 to 4;
n is 0, 1, 2 or 3;
R6 is arylene of from 6 to 10 carbon atoms;
and Z' and Z" are individually N or CH. - 4. A device as defined in claim 2, wherein said optical brightener is selected from the group consisting of 4,4'-bis(5,7-di-t-pentyl-2-benzoxazolyl)-stilbene; 2,5-bis(5,7-di-t-pentyl-2-benzoxazolyl)-1,3,4-thiadiazole; 2,5-bis(5,7-di-t-phenyl-2-benzoxazolyl)thiophene; 2,2'-p-(phenylenedi-vinylene)bisbenzothiazo1e; 4,4'-bis(2-benzoxazolyl)biphenyl; 2,5-bis15-(.alpha.,.alpha.-dimethyl-benzyl)-2-benzoxazolyl]-thiophene; 4,4'-bis[5,7-di-(2-methyl-2-butyl)-2-benznxazolyl]-stilbene; and 2,5-bis[5,7-ti-(2-methyl-2-butyl)-2-benzoxazolyl]-3,4-diphenylthiophene.
- 5. A device as defined in claim 1, wherein said electron-transporting compound is a metal complex of 8-hydroxyquinoline.
- 6. A device as defined in claim 5, wherein the metal of said metal complex is either Zn, Al, Mg or Li.
- 7. In an electroluminescent device compris-ing, in sequence, an anode electrode, a hole-injecting zone, an organic luminescent zone, and a cathode elec-trode, at least one of said electrodes being capable of transmitting at least 80% of radiation having wave-lengths longer than 400 nm, the improvement wherein said hole-injecting zone comprises an amine that transmits at least about 90% of radiation having wave-lengths greater than 400 nm, at least one nitrogen atom of the amine being trisubstituted with substitu-ents at least one of which is aryl, said amine being solid at room temperature and having the structural formula *
wherein:
Q1 and Q2 are individually moieties con-taining nitrogen and at least 3 carbocyclic rings at least one of which is aromatic, and G is a linking group or a carbon-to-carbon bond, whereby said amine is thin-film-forming. - 8. A device as defined in claim 7, wherein said hole-transporting compound is selected from the group consisting of bis(4-dimethylamino-2-methylphenyl)phenylmethane;
N,N,N-tri(p-tolyl)amine;
1,1-bis(4-di-p-tolylaminophenyl)cyclohexane; and 1,1-bis(4-di-p-tolylaminophenyl)-4-phenyl-cyclohexane. - 9. In an electroluminescent device com-prising, in sequence, an anode electrode, a hole-injecting zone, an organic luminescent zone, and a cathode electrode, at least one of said electrodes being capable of transmitting at least 80% of radiation having wave-lengths longer than 400 nm, the improvement wherein said hole-injecting zone comprises 1,1-bis(4-di-p-tolylaminophenyl)cyclo-hexane;
and said luminescent zone comprises 2,5-bi6(5,7-di-t-pentyl-2-benzoxazolyl)-1,3,4-thiadiazole;
said two zones having a combined thickness no greater than about 1 micron.
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US06/478,938 US4539507A (en) | 1983-03-25 | 1983-03-25 | Organic electroluminescent devices having improved power conversion efficiencies |
US478,938 | 1983-03-25 |
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EP (1) | EP0120673B1 (en) |
JP (1) | JPH0632307B2 (en) |
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1983
- 1983-03-25 US US06/478,938 patent/US4539507A/en not_active Expired - Lifetime
- 1983-05-13 CA CA000428167A patent/CA1213662A/en not_active Expired
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1984
- 1984-03-21 DE DE8484301899T patent/DE3471683D1/en not_active Expired
- 1984-03-21 EP EP84301899A patent/EP0120673B1/en not_active Expired
- 1984-03-26 JP JP59058088A patent/JPH0632307B2/en not_active Expired - Lifetime
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EP0120673A3 (en) | 1986-01-02 |
US4539507A (en) | 1985-09-03 |
JPS59194393A (en) | 1984-11-05 |
EP0120673B1 (en) | 1988-06-01 |
JPH0632307B2 (en) | 1994-04-27 |
EP0120673A2 (en) | 1984-10-03 |
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