材料科学
能量转换效率
掺杂剂
电子迁移率
接受者
钙钛矿(结构)
聚合物
噻吩
化学工程
纳米技术
光电子学
兴奋剂
有机化学
复合材料
化学
工程类
物理
凝聚态物理
作者
Guofeng You,Qixin Zhuang,Lijun Wang,Xinyu Lin,Ding Zou,Zhenghuan Lin,Hongyu Zhen,Wenliu Zhuang,Qidan Ling
标识
DOI:10.1002/aenm.201903146
摘要
Abstract The rich molecular design of electron donor (D)–acceptor (A) polymers offers many valuable clues to obtain high‐efficiency hole‐transporting materials (HTMs) for use in perovskite solar cells (PVSCs). The fused aromatic or heteroaromatic units can increase the conjugation of the polymer backbone to facilitate electron delocalization, which increases the rigidity of adjacent units to prevent rotational disorder and lower the reorganization energy, leading to improved carrier mobility and optimized film morphology. In this work, fused‐ring ladder‐type indacenodithiophene and indacenodithieno[3,2‐b]thiophene are used as D units, benzodithiophene‐4,8‐dione as the A unit, and thienothiophene as a π‐bridge to form the D–A polymers PBDTT and PBTTT, respectively. Both polymers exhibit favorable properties as HTMs including suitable energy levels, high hole mobility, and excellent film quality. Both dopant‐free HTMs endow n‐i‐p PVSCs with promising performance and stability. A maximum power conversion efficiency of 20.28% is achieved for PBDTT‐based devices, which is among the highest values reported to date.
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