期刊
JOURNAL OF MATERIALS CHEMISTRY C
卷 4, 期 31, 页码 7478-7484出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6tc01886f
关键词
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资金
- National Natural Science Foundation of China [51373054, 51573055, 51473052, 21334002]
- National Basic Research Program of China (973 Program) [2015CB655003, 2013CB834705]
- Fundamental Research Funds for the Central Universities
- Introduced Innovative R&D Team of Guangdong [201101C0105067115]
Efficient organic electroluminescent materials with both high solid-state fluorescence efficiency and high excitons usage efficiency for use in organic light-emitting diodes (OLEDs) are relatively rare. We report two isomeric-phenylethylene compounds with different positions and spatial orientation of the -CN substituent on the vinylene groups, namely alpha-CN-APV and beta-CN-APV. The synthesis, characterization, crystal structure, optical, electrochemical, thermal, and electroluminescence (EL) properties of the two compounds are discussed in detail. The crystal structure of the beta-CN-APV shows tight solid-state organization because of two, oppositely pointed, vertically aligned, hydrogen bonds between the two cyano groups and the two vinylene hydrogens (CN center dot center dot center dot H-C = C), while the alpha-CN-APV showed more flexible molecular structure with absence of vinylene hydrogen intermolecular interactions in the crystal. Such tight intermolecular stacking of beta-CN-APV ensures the high solid-state fluorescence quantum efficiency. Both the compounds exhibit hybrid local and charge transfer (HLCT) excited states, which facilitate the population of singlet excitons through the reverse intersystem crossing (RISC) process from the high lying triplet states. Experimental and theoretical investigation indicated that the beta-CN-APV, when compared to the alpha-CN-APV, showed higher solid-state fluorescence quantum efficiency and also higher excitons usage efficiency, which eventually provided much higher external quantum efficiency and brightness in the corresponding EL devices.
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