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- Publisher Website: 10.1021/cm201789u
- Scopus: eid_2-s2.0-84862907935
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Article: High efficiency nondoped deep-blue organic light emitting devices based on imidazole-π-triphenylamine derivatives
Title | High efficiency nondoped deep-blue organic light emitting devices based on imidazole-π-triphenylamine derivatives |
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Authors | |
Keywords | Nondoped Deep-blue emissions High current densities Organic light-emitting devices Triphenylamine derivatives |
Issue Date | 2012 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/cm |
Citation | Chemistry of Materials, 2012, v. 24 n. 1, p. 61-70 How to Cite? |
Abstract | High-performance deep-blue emitting phenanthroimidazole derivatives with a structure of donor-linker-acceptor were designed and synthesized. By using different linkers and different linking positions, four deep-blue emitters were obtained and used as emitters or bifunctional hole-transporting emitters in OLEDs. Such devices show low turn-on voltages (as low as 2.8 V), high efficiency (2.63 cd/A, 2.53 lm/W, 3.08%), little efficiency roll-off at high current densities, and stable deep-blue emissions with CIE y < 0.10. Performances are among the best comparing to recently reported deep-blue emitting devices with similar structures. The results suggest that the combination of the phenanthroimidazole and the donor-linker-acceptor structure can be an important approach for developing high performance deep-blue emitters in particular for lighting applications. © 2011 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/159304 |
ISSN | 2023 Impact Factor: 7.2 2023 SCImago Journal Rankings: 2.421 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zhang, Y | en_US |
dc.contributor.author | Lai, SL | en_US |
dc.contributor.author | Tong, QX | en_US |
dc.contributor.author | Lo, MF | en_US |
dc.contributor.author | Ng, TW | en_US |
dc.contributor.author | Chan, MY | en_US |
dc.contributor.author | Wen, ZC | en_US |
dc.contributor.author | He, J | en_US |
dc.contributor.author | Jeff, KS | en_US |
dc.contributor.author | Tang, XL | en_US |
dc.contributor.author | Liu, WM | en_US |
dc.contributor.author | Ko, CC | en_US |
dc.contributor.author | Wang, PF | en_US |
dc.contributor.author | Lee, CS | en_US |
dc.date.accessioned | 2012-08-16T05:48:32Z | - |
dc.date.available | 2012-08-16T05:48:32Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Chemistry of Materials, 2012, v. 24 n. 1, p. 61-70 | en_US |
dc.identifier.issn | 0897-4756 | - |
dc.identifier.uri | http://hdl.handle.net/10722/159304 | - |
dc.description.abstract | High-performance deep-blue emitting phenanthroimidazole derivatives with a structure of donor-linker-acceptor were designed and synthesized. By using different linkers and different linking positions, four deep-blue emitters were obtained and used as emitters or bifunctional hole-transporting emitters in OLEDs. Such devices show low turn-on voltages (as low as 2.8 V), high efficiency (2.63 cd/A, 2.53 lm/W, 3.08%), little efficiency roll-off at high current densities, and stable deep-blue emissions with CIE y < 0.10. Performances are among the best comparing to recently reported deep-blue emitting devices with similar structures. The results suggest that the combination of the phenanthroimidazole and the donor-linker-acceptor structure can be an important approach for developing high performance deep-blue emitters in particular for lighting applications. © 2011 American Chemical Society. | - |
dc.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/cm | - |
dc.relation.ispartof | Chemistry of Materials | en_US |
dc.subject | Nondoped | - |
dc.subject | Deep-blue emissions | - |
dc.subject | High current densities | - |
dc.subject | Organic light-emitting devices | - |
dc.subject | Triphenylamine derivatives | - |
dc.title | High efficiency nondoped deep-blue organic light emitting devices based on imidazole-π-triphenylamine derivatives | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chan, MY: chanmym@hku.hk | en_US |
dc.identifier.authority | Chan, MY=rp00666 | en_US |
dc.identifier.doi | 10.1021/cm201789u | - |
dc.identifier.scopus | eid_2-s2.0-84862907935 | - |
dc.identifier.hkuros | 203480 | en_US |
dc.identifier.volume | 24 | en_US |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 61 | en_US |
dc.identifier.epage | 70 | en_US |
dc.identifier.isi | WOS:000298908400011 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0897-4756 | - |