CONTAMINANT-SCAVENGING LAYER ON OLED ANODES
An OLED includes an anode formed over a substrate and a contaminant-scavenging layer formed over the anode, wherein the contaminant-scavenging layer includes one or more organic materials but not a hexaazatriphenylene derivative, each having an electron-accepting property and a reduction potential greater than −0.1 V vs. a Saturated Calomel Electrode, and wherein the one or more organic materials provide more than 50% by mole ratio of the contaminant-scavenging layer. The OLED also includes an organic electroluminescent unit formed over the contaminant-scavenging layer, wherein the organic electroluminescent unit includes a hole-transporting layer, a light-emitting layer, and an electron-transporting layer, and a cathode formed over the organic electroluminescent unit.
1 . A method of forming an OLED, comprising:
a) providing a substrate, which includes one or more anodes, into a vacuum chamber or inert atmosphere environment where such substrate resides for at least 30 min before subsequent processing; deforming an anode over a substrate;
b) forming a contaminant-scavenging layer over the anode(s), wherein the contaminant-scavenging layer includes one or more organic materials, each having an electron-accepting property and a reduction potential greater than −0.1 V vs. a Saturated Calomel Electrode, and wherein the one or more organic materials provide more than 50% by mole ratio of the contaminant-scavenging layer;
c) forming an organic electroluminescent unit over the contaminant-scavenging layer; and
d) forming a cathode over the organic electroluminescent unit.
2 . The method according to claim 1 wherein forming the contaminant-scavenging layer including a chemical compound
3 . The method according to claim 1 wherein forming the contaminant-scavenging layer including a chemical compound
wherein R 1 -R 4 represent hydrogen or substituents independently selected from the group including nitrile (—CN), nitro (—NO 2 ), sulfonyl (—SO 2 R), sulfoxide (—SOR), trifluoromethyl (—CF 3 ), ester (—CO—OR), amide (—CO—NHR or —CO—NRR′), substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, and substituted or unsubstituted alkyl, where R and R′ include substituted or unsubstituted alkyl or aryl; or wherein R 1 and R 2 , or R 3 and R 4 , combine form a ring structure including an aromatic ring, a heteroaromatic ring, or a non-aromatic ring, and each ring is substituted or unsubstituted.
4 . The method according to claim 1 wherein forming the contaminant-scavenging layer including a chemical compound
wherein R 1 -R 6 represent hydrogen or a substituent independently selected from the group including halo, nitrile (—CN), nitro (—NO 2 ), sulfonyl (—SO 2 R), sulfoxide (—SOR), trifluoromethyl (—CF 3 ), ester (—CO—OR), amide (—CO—NHR or —CO—NRR′), substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, and substituted or unsubstituted alkyl, where R and R′ include substituted or unsubstituted alkyl or aryl; or wherein R 1 and R 2 , R 3 and R 4 , or R 5 and R 6 , combine form a ring structure including an aromatic ring, a heteroaromatic ring, or a non-aromatic ring, and each ring is substituted or unsubstituted.
5 . The method according to claim 1 wherein forming the contaminant-scavenging layer including a chemical compound
6 . A method of forming an OLED, comprising:
a) Providing a substrate, which includes one or more anodes;
b) forming a contaminant-scavenging layer over the anode(s), wherein the contaminant-scavenging layer includes one or more organic materials, each having an electron-accepting property and a reduction potential greater than −0.1 V vs. a Saturated Calomel Electrode, and wherein the one or more organic materials provide more than 50% by mole ratio of the contaminant-scavenging layer;
b) providing the substrate having the contaminant-scavenging layer into a vacuum chamber or inert atmosphere environment where the substrate resides for at least 30 min before subsequent processing;
d) forming an organic electroluminescent unit over the contaminant-scavenging layer; and
e) forming a cathode over the organic electroluminescent unit.
7 . The method according to claim 5 wherein forming the contaminant-scavenging layer including a chemical compound
8 . The method according to claim 5 wherein forming the contaminant-scavenging layer including a chemical compound
wherein R 1 -R 4 represent hydrogen or substituents independently selected from the group including nitrile (—CN), nitro (—NO 2 ), sulfonyl (—SO 2 R), sulfoxide (—SOR), trifluoromethyl (—CF 3 ), ester (—CO—OR), amide (—CO—NHR or —CO—NRR′), substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, and substituted or unsubstituted alkyl, where R and R′ include substituted or unsubstituted alkyl or aryl; or wherein R 1 and R 2 , or R 3 and R 4 , combine form a ring structure including an aromatic ring, a heteroaromatic ring, or a non-aromatic ring, and each ring is substituted or unsubstituted.
9 . The method according to claim 5 wherein forming the contaminant-scavenging layer including a chemical compound
wherein R 1 -R 6 represent hydrogen or a substituent independently selected from the group including halo, nitrile (—CN), nitro (—NO 2 ), sulfonyl (—SO 2 R), sulfoxide (—SOR), trifluoromethyl (—CF 3 ), ester (—CO—OR), amide (—CO—NHR or —CO—NRR′), substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, and substituted or unsubstituted alkyl, where R and R′ include substituted or unsubstituted alkyl or aryl; or wherein R 1 and R 2 , R 3 and R 4 , or R 5 and R 6 , combine form a ring structure including an aromatic ring, a heteroaromatic ring, or a non-aromatic ring, and each ring is substituted or unsubstituted.
10 . The method according to claim 5 wherein forming the contaminant-scavenging layer including a chemical compound