4.8 Article

Structurally robust phosphorescent [Pt(ONCN)] emitters for high performance organic light-1

期刊

CHEMICAL SCIENCE
卷 5, 期 12, 页码 4819-4830

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4sc01105h

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资金

  1. Theme-Based Research Scheme [T23-713/11]
  2. National Key Basic Research Program of China [2013CB834802]
  3. Research Grants Council of Hong Kong SAR [HKU 700812]
  4. National Science Foundation of China [61274002]
  5. Innovation and Technology Commission of the HKSAR Government [GHP/043/10]
  6. Guangdong Special Project of the Introduction of Innovative RD Teams
  7. GuangDong Aglaia Optoelectronic Materials Co., Ltd.
  8. University of Hong Kong
  9. [201309176101]

向作者/读者索取更多资源

A series of robust, bulky and strongly emissive platinum(II) complexes supported by tetradentate O boolean AND N boolean AND C boolean AND 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 boolean AND N boolean AND C boolean AND 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 lambda(max) in the range of 522 to 570 nm, and have a good thermal stability of up to T-d > 423 degrees C. Notably, the k(q) values of 4-6 are in the range of 8.5 x 10(6) to 2.0 x 10(7) mol(-1) dm(3) s(-1), smaller than those (similar to 10(8) to 10(9) mol(-1) dm(3) s(-1)) of other reported Pt(II) complexes. The bulky groups at the periphery of the [O boolean AND N boolean AND C boolean AND 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.

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