IP Library Granted Patent US 8,911,883
Granted Patent B2
US 8,911,883 · App. 12/219,231 · Granted Dec 16, 2014

Photosensitive semiconductor nanocrystals, photosensitive composition comprising semiconductor nanocrystals and method for forming semiconductor nanocrystal pattern using the same

Inventors: Jong Jin Park (Gyeonggi-Do, KR); Eun Joo Jang (Gyeonggi-Do, KR); Shin Ae Jun (Gyeonggi-Do, KR); Tae Kyung Ahn (Seoul-Si, KR); Sung Hun Lee (Gyeonggi-Do, KR)
Assignee: Samsung Electronics Co., Ltd.
C08F2/28C30B29/60H01L51/426G03F7/027Y10S977/773C30B33/00G03F7/0047Y02E10/549B82Y20/00B82Y30/00G03F7/0043Y10S428/917
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Quick Facts
Patent No.
US 8,911,883
App. No.
12/219,231
Granted
Dec 16, 2014
Kind
B2
Abstract

An organic-inorganic hybrid electroluminescent device having a semiconductor nanocrystal pattern prepared by producing a semiconductor nanocrystal film using semiconductor nanocrystals, where the nanocrystal is surface-coordinated with a compound containing a photosensitive functional group, exposing the film through a mask and developing the exposed film.

Claims (33)

1. An organic-inorganic hybrid electroluminescent device comprising:

a semiconductor nanocrystal pattern prepared by

coating a substrate with a dispersion in an organic solvent of semiconductor nanocrystals, wherein the semiconductor nanocrystals are surface-coordinated with a compound containing photosensitive functional groups;

evaporating the organic solvent to form a film of the surface-coordinated semiconductor nanocrystals on the substrate;

exposing the film to light through a mask;

cross-linking the photosensitive functional groups to form a network structure of the semiconductor nanocrystals; and

developing the exposed film,

wherein the compound containing a photosensitive functional group is represented by Formula 1 below:

X-A-B  (1),

wherein X is NC—, HOOC—, HRN—, POOOH—, RS— or RSS—, in which R is a hydrogen atom or a C 1˜10 saturated or unsaturated aliphatic hydrocarbon group;

A is a direct bond, a saturated aliphatic hydrocarbon group, a phenylene group, a biphenylene group, an aliphatic ester group, an aliphatic amide group, an aliphatic oxycarbonyl group or an aliphatic ether group; and

B is an organic group containing at least one carbon-carbon double bond, which may be substituted with at least one group selected from the group consisting of —CN, —COOH, halogen groups, C 1˜5 halogenated alkyl groups, amine groups, C 6˜15 aromatic hydrocarbon groups, and C 6˜12 aromatic hydrocarbon groups substituted with F, Cl, Br, a halogenated alkyl group, R′O—, in which R′ is a hydrogen atom or a C 1˜5 alkyl group, —COOH, an amine group, or —NO 2 .

2. The organic-inorganic hybrid electroluminescent device according to claim 1 , wherein the moiety B in Formula 1 is an organic group represented by Formula 2 below:

—CR 1 ═CR 2 R 3   (2)

wherein R 1 is a hydrogen atom, —COOH, a halogen group, a C 1˜5 alkyl group or a halogenated alkyl group; and R 2 and R 3 are each independently a hydrogen atom, a C 1˜30 alkyl group, —CN, —COOH, a halogen group, a C 1˜5 halogenated alkyl group, a C 2˜30 unsaturated aliphatic hydrocarbon group containing at least one carbon-carbon double bond, a C 6˜12 aromatic hydrocarbon group substituted or unsubstituted with F, Cl, Br, hydroxyl, a C 1˜5 halogenated alkyl group, an amine group, R′O—, in which R′ is a C 1˜5 alkyl group, —COOH, or —NO 2 .

3. The organic-inorganic hybrid electroluminescent device according to claim 1 , wherein the compound containing a photosensitive functional group is selected from a group consisting of acrylic acid compounds, unsaturated fatty acid compounds, cinnamic acid compounds, vinylbenzoic acid compounds, acrylonitrile-based compounds, unsaturated nitrile-based compounds, unsaturated amine compounds, and unsaturated sulfide compounds.

4. The organic-inorganic hybrid electroluminescent device according to claim 1 , wherein the compound containing a photosensitive functional group is selected from a group consisting of methacrylic acid, crotonic acid, vinylacetic acid, tiglic acid, 3,3-dimethylacrylic acid, trans-2-pentenoic acid, 4-pentenoic acid, trans-2-methyl-2-pentenoic acid, 2,2-dimethyl-4-pentenoic acid, trans-2-hexenoic acid, trans-3-hexenoic acid, 2-ethyl-2-hexenoic acid, 6-heptenoic acid, 2-octenoic acid, citronellic acid, undecylenic acid, myristoleic acid, palmitoleic acid, oleic acid, elaidic acid, cis-11-elcosenoic acid, euric acid, nervonic acid, trans-2,4-pentadienoic acid, 2,4-hexadienoic acid, 2,6-heptadienoic acid, geranic acid, linoleic acid, 11,14-eicosadienoic acid, cis-8,11,14-eicosatrienoic acid, arachidonic acid, cis-5,8,11,14,17-eicosapentaenoic acid, cis-4,7,10,13,16,19-docosahexaenoic acid, fumaric acid, maleic acid, itaconic acid, ciraconic acid, mesaconic acid, trans-glutaconic acid, trans-beta-hydromuconic acid, trans-traumatic acid, trans-muconic acid, cis-aconitic acid, trans-aconitic acid, cis-3-chloroacrylic acid, trans-3-chloroacrylic acid, 2-bromoacrylic acid, 2-(trifluoromethyl)acryl-ic acid, trans-styrylacetic acid, trans-cinnamic acid, alpha.-methylcinnamic acid, 2-methylcinnamic acid, 2-fluorocinnamic acid, 2-(trifluoromethyl)cinnamic acid, 2-chlorocinnamic acid, 2-methoxycinnamic acid, 2-hydroxycinnamic acid, 2-nitrocinnamic acid, 2-carboxycinnamic acid, trans-3-fluorocinnamic acid, 3-(trifluoromethyl)cinnamic acid, 3-chlorocinnamic acid, 3-bromocinnamic acid, 3-methoxycinnamic acid, 3-hydroxycinnamic acid, 3-nitrocinnamic acid, 4-methylcinnamic acid, 4-fluorocinnamic acid, trans-4-(trifluoromethyl)-cinnamic acid, 4-chlorocinnamic acid, 4-bromocinnamic acid, 4-methoxycinnamic acid, 4-hydroxycinnamic acid, 4-nitrocinnamic acid, 3,3-dimethoxycinnamic acid, 4-vinylbenzoic acid, allyl methyl sulfide, allyl disulfide, diallyl amine, oleylamine, 3-amino-1-propanol vinyl ether, 4-chlorocinnamonitrile, 4-methoxycinnamonitrile, 3,4-dimethoxycinnamonitrile, 4-dimethylaminocinnamonitrile, acrylonitrile, allyl cyanide, crotononitrile, methacrylonitrile, cis-2-pentenenitrile, trans-3-pentenenitrile, 3,7-dimethyl-2,6-octadienenitrile, and 1,4-dicyano-2-butene.

5. The organic-inorganic hybrid electroluminescent device according to claim 1 , wherein the semiconductor nanocrystal comprises CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, HgS, HgSe, HgTe, GaN, GaP, GaAs, InP, InAs, or a mixture thereof.

6. The organic-inorganic hybrid electroluminescent device according to claim 5 , wherein the semiconductor nanocrystal comprises at least two compounds selected from the group consisting of CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, HgS, HgSe, HgTe, GaN, GaP, GaAs, InP and InAs, and is a uniformly mixed type, gradiently mixed type, core-shell type, or alloy type.

7. An article, comprising:

a semiconductor nanocrystal pattern prepared by

coating a substrate with a dispersion in an organic solvent of semiconductor nanocrystals, wherein the semiconductor nanocrystals are surface-coordinated with a compound containing photosensitive functional groups;

evaporating the organic solvent to form a film of the surface-coordinated semiconductor nanocrystals on the substrate;

exposing the film to light through a mask;

cross-linking the photosensitive functional groups to form a network structure of the semiconductor nanocrystals; and

developing the exposed film,

wherein the compound containing a photosensitive functional group is represented by Formula 1 below:

X-A-B  (1),

wherein X is NC—, HOOC—, HRN—, POOOH—, RS— or RSS—, in which R is a hydrogen atom or a C 1˜10 saturated or unsaturated aliphatic hydrocarbon group;

A is a direct bond, a saturated aliphatic hydrocarbon group, a phenylene group, a biphenylene group, an aliphatic ester group, an aliphatic amide group, an aliphatic oxycarbonyl group or an aliphatic ether group; and

B is an organic group containing at least one carbon-carbon double bond, which may be substituted with at least one group selected from the group consisting of —CN, —COOH, halogen groups, C 1˜5 halogenated alkyl groups, amine groups, C 6˜15 aromatic hydrocarbon groups, and C 6˜12 aromatic hydrocarbon groups substituted with F, Cl, Br, a halogenated alkyl group, R′O—, in which R′ is a hydrogen atom or a C 1˜5 alkyl group, —COOH, an amine group, or —NO 2 .

8. The organic-inorganic hybrid electroluminescent device of claim 1 , wherein the exposing further comprises exposing the film at an exposure dose of 50 millijoules per square centimeter to 850 millijoules per square centimeter.

9. The organic-inorganic hybrid electroluminescent device of claim 1 , wherein the exposing further comprises exposing the film to light having a wavelength of 200 nanometers to 500 nanometers and an energy of 100 watts to 800 watts.

Priority Claims (1)
KR 2003-73338 · Oct 21, 2003 · national
Continuity (3)
Division 11378482 · Mar 20, 2006
Division 10814264 · Apr 1, 2004
Related Publication 20080290797A1 · Nov 27, 2008