有机发光二极管
材料科学
共发射极
准分子
荧光
深铬移
光电子学
电致发光
咔唑
光化学
量子效率
兴奋剂
激子
掺杂剂
分析化学(期刊)
光学
纳米技术
化学
物理
图层(电子)
量子力学
色谱法
作者
Yiyun Chen,Yu‐Cheng Kung,Miaosheng Wang,Yuan‐Chih Lo,Yao‐Te Chia,Chun‐Kai Wang,Deng‐Gao Chen,Ju‐Ting Cheng,Pi‐Tai Chou,Chi-Chi Wu,Elise Y. Li,Bin Hu,Wen‐Yi Hung,Ken‐Tsung Wong
标识
DOI:10.1002/adom.202303131
摘要
Abstract Two blends comprising new dicyanopyrazine‐based acceptors ( m ‐CN and p ‐CN ) and a carbazole‐based donor CPTBF are explored for exciplex formation. The CPTBF: m ‐CN and CPTBF: p ‐CN blends show the signature red‐shifted emission together with the delayed fluorescence observed in time‐resolved measurement, manifesting the characteristics of thermally activated delayed fluorescence (TADF). The electroluminescence (EL) device employing CPTBF: m ‐CN ( CPTBF: p ‐CN ) blend as the emitting layer (EML) achieved an EQE of 5.22% (2.05%) with the EL λ max centered at 607 nm (625 nm). The exciplex excitons can be efficiently extracted by a new benzobisthiadiazole‐based near‐infrared (NIR) emitter DCzPBBT , where a device is configured with CPTBF: m ‐CN : (5 wt.%) DCzPBBT as the EML to achieve a high EQE of 5.32% and an EL λ max 758 nm. Further increase of the doping concentration to 10 wt.% of DCzPBBT exhibits a bathochromic shifted EL λ max to 772 nm with 94% spectral coverage in the NIR (>700 nm) region, while the device EQE retains at 4.06%. The superior device performance stems from the highly efficient energy transfer between the exciplex‐forming host and NIR dopant together.
科研通智能强力驱动
Strongly Powered by AbleSci AI