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Article: Structurally robust phosphorescent [Pt(O^N^C^N)] emitters for high performance organic light-emitting devices with power efficiency up to 126 lm W-1 and external quantum efficiency over 20%
Title | Structurally robust phosphorescent [Pt(O^N^C^N)] emitters for high performance organic light-emitting devices with power efficiency up to 126 lm W-1 and external quantum efficiency over 20% |
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Authors | |
Issue Date | 2014 |
Citation | Chemical Science, 2014, v. 5, n. 12, p. 4819-4830 How to Cite? |
Abstract | © the Partner Organisations 2014. A series of robust, bulky and strongly emissive platinum(ii) complexes supported by tetradentate O^N^C^N ligands with tert-butyl groups (1-4), a bridging tertiary amine (5) or a biphenyl group with a spiro linkage (6) at the periphery of the [O^N^C^N] ligand scaffold have been prepared. Their photophysical properties were examined by absorption and emission spectroscopy, density functional theory calculations, and ultra-fast time-resolved emission measurements. These complexes display emission quantum yields of up to 95%, with emission maxima λmax in the range of 522 to 570 nm, and have a good thermal stability of up to Td > 423 °C. Notably, the kq values of 4-6 are in the range of 8.5 × 106 to 2.0 × 107 mol-1 dm3 s-1, smaller than those (∼108 to 109 mol-1 dm3 s-1) of other reported Pt(ii) complexes. The bulky groups at the periphery of the [O^N^C^N] ligand disfavour intermolecular interactions and hence excimer formation in solutions. These complexes are good light-emitting materials (dopants) for OLEDs, since the triplet-triplet annihilation (TTA) and concentration quenching effect arising from intermolecular interactions can be minimized even at a high dopant concentration. The efficiency of the devices fabricated with 4-6 increased with dopant concentration up to a high level of 10% with no extra emitting component or significant shift in the CIE observed. The maximum power efficiency (PE) values achieved for the 5 (yellow-emitting) and 6 (green-emitting) based devices were 118 and 126 lm W-1, respectively. These PE values are the highest among the reported Pt(ii)-OLEDs and comparable to those of the best reported Ir(iii)-OLEDs without the out-coupling technique. Complex 7 is structurally analogous to, but less bulky than 3-6 and is prone to giving excimer emission in the solid state. A high PE of up to 55.5 lm W-1 and external quantum efficiency of up to 25.1% have been realized in the white OLEDs fabricated with 7 as a single emitting material. These values are comparable with those of the best reported WOLEDs based on a single emitting material. This journal is |
Persistent Identifier | http://hdl.handle.net/10722/225901 |
ISSN | 2023 Impact Factor: 7.6 2023 SCImago Journal Rankings: 2.333 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Cheng, Gang | - |
dc.contributor.author | Kui, Steven C F | - |
dc.contributor.author | Ang, Wai Hung | - |
dc.contributor.author | Ko, Man Ying | - |
dc.contributor.author | Chow, Pui Keong | - |
dc.contributor.author | Kwong, Chun Lam | - |
dc.contributor.author | Kwok, Chi Chung | - |
dc.contributor.author | Ma, Chensheng | - |
dc.contributor.author | Guan, Xiangguo | - |
dc.contributor.author | Low, Kam Hung | - |
dc.contributor.author | Su, Shi Jian | - |
dc.contributor.author | Che, Chi Ming | - |
dc.date.accessioned | 2016-05-23T02:22:07Z | - |
dc.date.available | 2016-05-23T02:22:07Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Chemical Science, 2014, v. 5, n. 12, p. 4819-4830 | - |
dc.identifier.issn | 2041-6520 | - |
dc.identifier.uri | http://hdl.handle.net/10722/225901 | - |
dc.description.abstract | © the Partner Organisations 2014. A series of robust, bulky and strongly emissive platinum(ii) complexes supported by tetradentate O^N^C^N ligands with tert-butyl groups (1-4), a bridging tertiary amine (5) or a biphenyl group with a spiro linkage (6) at the periphery of the [O^N^C^N] ligand scaffold have been prepared. Their photophysical properties were examined by absorption and emission spectroscopy, density functional theory calculations, and ultra-fast time-resolved emission measurements. These complexes display emission quantum yields of up to 95%, with emission maxima λmax in the range of 522 to 570 nm, and have a good thermal stability of up to Td > 423 °C. Notably, the kq values of 4-6 are in the range of 8.5 × 106 to 2.0 × 107 mol-1 dm3 s-1, smaller than those (∼108 to 109 mol-1 dm3 s-1) of other reported Pt(ii) complexes. The bulky groups at the periphery of the [O^N^C^N] ligand disfavour intermolecular interactions and hence excimer formation in solutions. These complexes are good light-emitting materials (dopants) for OLEDs, since the triplet-triplet annihilation (TTA) and concentration quenching effect arising from intermolecular interactions can be minimized even at a high dopant concentration. The efficiency of the devices fabricated with 4-6 increased with dopant concentration up to a high level of 10% with no extra emitting component or significant shift in the CIE observed. The maximum power efficiency (PE) values achieved for the 5 (yellow-emitting) and 6 (green-emitting) based devices were 118 and 126 lm W-1, respectively. These PE values are the highest among the reported Pt(ii)-OLEDs and comparable to those of the best reported Ir(iii)-OLEDs without the out-coupling technique. Complex 7 is structurally analogous to, but less bulky than 3-6 and is prone to giving excimer emission in the solid state. A high PE of up to 55.5 lm W-1 and external quantum efficiency of up to 25.1% have been realized in the white OLEDs fabricated with 7 as a single emitting material. These values are comparable with those of the best reported WOLEDs based on a single emitting material. This journal is | - |
dc.language | eng | - |
dc.relation.ispartof | Chemical Science | - |
dc.title | Structurally robust phosphorescent [Pt(O^N^C^N)] emitters for high performance organic light-emitting devices with power efficiency up to 126 lm W-1 and external quantum efficiency over 20% | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1039/c4sc01105h | - |
dc.identifier.scopus | eid_2-s2.0-84908417532 | - |
dc.identifier.hkuros | 244721 | - |
dc.identifier.volume | 5 | - |
dc.identifier.issue | 12 | - |
dc.identifier.spage | 4819 | - |
dc.identifier.epage | 4830 | - |
dc.identifier.eissn | 2041-6539 | - |
dc.identifier.isi | WOS:000344376400034 | - |
dc.identifier.issnl | 2041-6520 | - |