侧链
咔唑
材料科学
烷氧基
接受者
聚合物
钙钛矿(结构)
热稳定性
共聚物
掺杂剂
电子迁移率
共轭体系
高分子化学
光化学
化学工程
兴奋剂
有机化学
烷基
化学
光电子学
复合材料
工程类
物理
凝聚态物理
作者
Guofeng You,Lihua Li,Shuaiqi Wang,Jiabing Cao,Yao Lu,Wanzhu Cai,Zhonggao Zhou,Kan Li,Zhenghuan Lin,Hongyu Zhen,Qidan Ling
标识
DOI:10.1002/aenm.202102697
摘要
Abstract In conventional n–i–p perovskite solar cells (PVSCs), electron donor (D)–acceptor (A) polymers have been found to be potential substitutes for doped spiro‐based small molecule hole‐transporting materials (HTMs) due to their excellent performance in hole mobility, film formability, and stability. Herein, a benzo[1,2‐b:4,5‐b′]dithiophene (BDT)‐benzodithiophene‐4,8‐dione (BDD) copolymer PBDB‐Cz is developed by employing carbazole as the conjugated side chain of BDT. PBDB‐O and PBDB‐T with alkoxy and thiophene as the side chain of BDT, respectively, are also synthesized and studied for comparison. The synergistic effect of the carbazole side chain and the BDT‐BDD backbone to promote hole transport properties is found in PBDB‐Cz. The carbazole side chain enhances both coplanarity and interaction of polymer chains, while simultaneously deepening energy levels and improving the hole mobility of the polymeric HTM. Consequently, PBDB‐Cz outperforms two counterparts, exhibiting a promising power conversion efficiency (PCE) of 22.06%. Notably, the PBDB‐Cz also improves the device stability, and the devices can retain more than 90% of their initial PCEs after being stored at ambient conditions for 100 days. To the best of the authors’ knowledge, this is the first report to incorporate carbazole into D–A polymeric HTM by side chain engineering.
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