同音
噻吩
有机太阳能电池
能量转换效率
轨道能级差
化学
吸收(声学)
电子受体
分子
光化学
接受者
八面体
材料科学
结晶学
聚合物
有机化学
光电子学
晶体结构
金属
复合材料
物理
凝聚态物理
作者
Zhichao Yao,Xianwang Tao,Duoquan You,Jingsheng Wang,Kaiqi Lv,Huili Ma,Youtian Tao
标识
DOI:10.1016/j.orgel.2023.106857
摘要
Cyclometalated tris-Ir(III) complexes with six-coordinated octahedral configuration are beneficial to reduce aggregation for improved film morphology in organic solar cells (OSCs). Herein, two homoleptic tris-Ir complexes of eBz3Ir and eTBz3Ir showing majority absorption from UV to light-blue range are designed as electron donor materials. Owing to the extended π-conjugation by an extra thiophene ring in each ligand, eTBz3Ir exhibits red-shifted and stronger absorption as well as better charge transport property than eBz3Ir. Therefore, when employing the fused-ring non-fullerene acceptor Y6 or L8-BO to fabricate all-small-molecule OSCs (ASMOSCs), eTBz3Ir blended devices demonstrate higher efficiency than eBz3Ir, with maximum power conversion efficiency (PCE) achieving at 9.48/7.55% for Y6 and 10.48/6.46% for L8-BO devices, respectively. To our knowledge, over 10% PCE is among the highest values for binary ASMOSCs based on organometallic Ir complexes as photovoltaic materials. Such uncompetitive solar-light absorption but relatively high PCE indicates homoleptic Ir complexes with octahedral configurations are expected as promising photoactive materials for high-efficiency ASMOSCs.
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