掺杂剂
钙钛矿(结构)
钝化
材料科学
能量转换效率
热稳定性
相(物质)
图层(电子)
化学工程
纳米技术
光电子学
兴奋剂
化学
有机化学
工程类
作者
Jing Song,Haibing Xie,Eng Liang Lim,Yahong Li,Tengfei Kong,Yang Zhang,Xia Zhou,Chunhui Duan,Dongqin Bi
出处
期刊:Solar RRL
[Wiley]
日期:2022-01-06
卷期号:6 (4)
被引量:16
标识
DOI:10.1002/solr.202100880
摘要
All‐inorganic perovskites have attracted substantial interest due to their outstanding thermal stability. However, the device performance is still inferior to the typical organic–inorganic counterparts because of the unsatisfying phase stability and defects of the inorganic perovskite films. Herein, a multistrategy to optimize CsPbI 2 Br perovskite solar cells (PSCs) based on dopant‐free poly(3‐hexylthiophene) (P3HT) by applying thienylmethylamine acetate additive to enhance the α phase stability and passivate the bulk defects of CsPbI 2 Br perovskite is successfully demonstrated, followed by implementing BTCIC‐4Cl interlayer at CsPbI 2 Br/P3HT interface, which can coordinate with both perovskite and P3HT to suppress the surface defects and promote the hole transport. Benefitting from these, a champion power conversion efficiency (PCE) of 16.3% is achieved, and the unencapsulated optimized device can retain 97% of the initial PCE after aging under N 2 atmosphere at 85 °C for 530 h. This work opens up a new era of multistrategy for improving performance and stability of CsPbI 2 Br PSCs based on dopant‐free hole transport layer.
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