Is Excess PbI2 Beneficial for Perovskite Solar Cell Performance?

材料科学 钙钛矿(结构) 钝化 碘化物 粒度 氧化锡 化学工程 晶界 基质(水族馆) 能量转换效率 光电子学 氧化物 无机化学 纳米技术 冶金 微观结构 图层(电子) 海洋学 地质学 化学 工程类
作者
Fangzhou Liu,Qi Dong,Man‐Hon Wong,Aleksandra B. Djurišić,Annie Ng,Zhiwei Ren,Qian Shen,C. Surya,Wai Kin Chan,Jian Wang,Alan Man Ching Ng,Changzhong Liao,Hangkong Li,Kaimin Shih,Chengrong Wei,Huimin Su,Junfeng Dai
出处
期刊:Advanced Energy Materials [Wiley]
卷期号:6 (7) 被引量:363
标识
DOI:10.1002/aenm.201502206
摘要

Unreacted lead iodide is commonly believed to be beneficial to the efficiency of methylammonium lead iodide perovskite based solar cells, since it has been proposed to passivate the defects in perovskite grain boundaries. However, it is shown here that the presence of unreacted PbI 2 results in an intrinsic instability of the film under illumination, leading to the film degradation under inert atmosphere and faster degradation upon exposure to illumination and humidity. The perovskite films without lead iodide have improved stability, but lower efficiency due to inferior film morphology (smaller grain size, the presence of pinholes). Optimization of the deposition process resulted in PbI 2 ‐free perovskite films giving comparable efficiency to those with excess PbI 2 (14.2 ± 1.3% compared to 15.1 ± 0.9%) Thus, optimization of the deposition process for PbI 2 ‐free films leads to dense, pinhole‐free, large grain size perovskite films which result in cells with high efficiency without detrimental effects on the film photostability caused by excess PbI 2 . However, it should be noted that for encapsulated devices illuminated through the substrate (fluorine‐doped tin oxide glass, TiO 2 film), film photostability is not a key factor in the device degradation.
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