材料科学
掺杂剂
钙钛矿(结构)
侧链
钝化
共轭体系
接受者
电子迁移率
聚合物
化学工程
烷基
能量转换效率
高分子化学
兴奋剂
纳米技术
有机化学
图层(电子)
光电子学
复合材料
化学
物理
凝聚态物理
工程类
作者
Zhiqing Xie,Jeonghyeon Park,Hyerin Kim,Bo Hyeon Cho,Chetan Lakshman,Ho‐Yeol Park,Thavamani Gokulnath,Young-Yong Kim,Jinhwan Yoon,Je‐Sung Jee,Y. R. Cho,Sung Ho Jin
标识
DOI:10.1021/acsami.3c15611
摘要
Dopant-free polymeric hole transport materials (HTMs) have attracted considerable attention in perovskite solar cells (PSCs) due to their high carrier mobilities and excellent hydrophobicity. They are considered promising candidates for HTMs to replace commercial Spiro-OMeTAD to achieve long-term stability and high efficiency in PSCs. In this study, we developed BDT-TA-BTASi, a conjugated donor−π–acceptor polymeric HTM. The donor benzo[1,2-b:4,5-b′]dithiophene (BDT) and acceptor benzotriazole (BTA) incorporated pendant siloxane, and alkyl side chains led to high hole mobility and solubility. In addition, BDT-TA-BTASi can effectively passivate the perovskite layer and markedly decrease the trap density. Based on these advantages, dopant-free BDT-TA-BTASi-based PSCs achieved an efficiency of over 21.5%. Furthermore, dopant-free BDT-TA-BTASi-based devices not only exhibited good stability in N2 (retaining 92% of the initial efficiency after 1000 h) but also showed good stability at high-temperature (60 °C) and -humidity conditions (80 ± 10%) (retaining 92 and 82% of the initial efficiency after 400 h). These results demonstrate that BDT-TA-BTASi is a promising HTM, and the study provides guidance on dopant-free polymeric HTMs to achieve high-performance PSCs.
科研通智能强力驱动
Strongly Powered by AbleSci AI