材料科学
钙钛矿(结构)
卤化物
能量转换效率
化学工程
结晶
氧化铟锡
退火(玻璃)
非阻塞I/O
钙钛矿太阳能电池
热稳定性
光伏系统
纳米技术
光电子学
无机化学
薄膜
复合材料
催化作用
有机化学
化学
工程类
生物
生态学
作者
Haixia Rao,Senyun Ye,Feidan Gu,Ziran Zhao,Zhiwei Liu,Zuqiang Bian,Chunhui Huang
标识
DOI:10.1002/aenm.201800758
摘要
Abstract All‐inorganic cesium lead halide (CsPbX 3 ) perovskites have emerged as promising photovoltaic materials owing to their superior thermal stability compared to traditional organic–inorganic hybrid counterparts. However, the CsPbX 3 perovskites generally need to be prepared at high‐temperature, which restricts their application in multilayer or flexible solar cells. Herein, the formation of CsPbX 3 perovskites at room‐temperature (RT) induced by dimethylsulphoxide (DMSO) coordination is reported. It is further found that a RT solvent (DMSO) annealing (RTSA) treatment is valid to control the perovskite crystallization dynamics, leading to uniform and void‐free films, and consequently a maximum power conversion efficiency (PCE) of 6.4% in the device indium tin oxide (ITO)/NiO x /RT‐CsPbI 2 Br/C 60 /Bathocuproine (BCP)/Ag, which is, as far as it is known, the first report of RT solution‐processed CsPbX 3 ‐based perovskite solar cells (PSCs). Moreover, the efficiency can be boosted up to 10.4% by postannealing the RTSA‐treated perovskite film at an optimal temperature of 120 °C. Profiting from the moderate temperature, flexible PSCs are also demonstrated with a maximum PCE of 7.3% for the first time. These results may stimulate further development of all‐inorganic CsPbX 3 perovskites and their application in flexible electronics.
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