掺杂剂
材料科学
分子间力
聚合物
非共价相互作用
平面的
化学物理
堆积
钙钛矿(结构)
纳米技术
结晶学
分子
化学
光电子学
兴奋剂
氢键
有机化学
计算机图形学(图像)
复合材料
计算机科学
作者
Zhaoyang Yao,Yaxiao Guo,Lanlan He,Jiaxin Guo,Yu Guo,Fuguo Zhang,Linqin Wang,Hao Yang,Chenhao Xiao,Yi Liu,Yongsheng Chen,Licheng Sun
标识
DOI:10.1002/anie.202114341
摘要
Adequate hole mobility is the prerequisite for dopant-free polymeric hole-transport materials (HTMs). Constraining the configurational variation of polymer chains to afford a rigid and planar backbone can reduce unfavorable reorganization energy and improve hole mobility. Herein, a noncovalent conformational locking via S-O secondary interaction is exploited in a phenanthrocarbazole (PC) based polymeric HTM, PC6, to fix the molecular geometry and significantly reduce reorganization energy. Systematic studies on structurally explicit repeats to targeted polymers reveals that the broad and planar backbone of PC remarkably enhances π-π stacking of adjacent polymers, facilitating intermolecular charge transfer greatly. The inserted "Lewis soft" oxygen atoms passivate the trap sites efficiently at the perovskite/HTM interface and further suppress interfacial recombination. Consequently, a PSC employing PC6 as a dopant-free HTM offers an excellent power conversion efficiency of 22.2 % and significantly improved longevity, rendering it as one of the best PSCs based on dopant-free HTMs.
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