电致发光
量子产额
量子效率
共聚物
材料科学
接受者
光化学
光电子学
聚合物
轨道能级差
发光
二极管
有机发光二极管
荧光
化学
光学
纳米技术
物理
分子
有机化学
复合材料
凝聚态物理
图层(电子)
作者
Yinfeng Wang,Meng Li,Jin‐Ming Teng,He‐Ye Zhou,Wenlong Zhao,Chuan‐Feng Chen
标识
DOI:10.1002/ange.202110794
摘要
Abstract A strategy of chiral donor–acceptor copolymerization is proposed to develop chiral nonconjugated polymers with thermally activated delayed fluorescence (TADF). Based on this strategy, two pairs of chiral polymers ( R , R )‐/( S , S )‐ pTpAcDPS and ( R , R )‐/( S , S )‐ pTpAcBP were synthesized. The alternating copolymerization of the chiral donors and acceptors could effectively separate the frontier molecular orbitals, which made the polymers show small Δ E ST of 0.01–0.03 eV and efficient TADF properties. Moreover, the polymers also showed the quantum yield of up to 92 % and the circularly polarized luminescence. The solution‐processed circularly polarized organic light‐emitting diodes showed circularly polarized electroluminescence signals with high external quantum efficiencies of up to 22.1 % and maximum luminance of up to 34350 cd m −2 . This is the first report of CP‐OLEDs based on chiral TADF polymer, which provides a useful and valuable guidance for the development of high‐efficiency CPEL polymers.
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