卤化物
钙钛矿(结构)
碘化物
相(物质)
材料科学
串联
带隙
乙二胺
化学工程
化学
无机化学
光电子学
结晶学
有机化学
工程类
复合材料
作者
Taiyang Zhang,M. Ibrahim Dar,Ge Li,Feng Xu,Nanjie Guo,Michaël Grätzel,Yixin Zhao
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2017-09-01
卷期号:3 (9)
被引量:594
标识
DOI:10.1126/sciadv.1700841
摘要
Among various all-inorganic halide perovskites exhibiting better stability than organic-inorganic halide perovskites, α-CsPbI3 with the most suitable band gap for tandem solar cell application faces an issue of phase instability under ambient conditions. We discovered that a small amount of two-dimensional (2D) EDAPbI4 perovskite containing the ethylenediamine (EDA) cation stabilizes the α-CsPbI3 to avoid the undesirable formation of the nonperovskite δ phase. Moreover, not only the 2D perovskite of EDAPbI4 facilitate the formation of α-CsPbI3 perovskite films exhibiting high phase stability at room temperature for months and at 100°C for >150 hours but also the α-CsPbI3 perovskite solar cells (PSCs) display highly reproducible efficiency of 11.8%, a record for all-inorganic lead halide PSCs. Therefore, using the bication EDA presents a novel and promising strategy to design all-inorganic lead halide PSCs with high performance and reliability.
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