化学
钝化
铟
钙钛矿(结构)
化学工程
纳米技术
无机化学
光电子学
结晶学
有机化学
图层(电子)
物理
工程类
材料科学
作者
Guijie Liang,W. W. Zhang,Jiawei Song,Jiahao Cheng,P. T. Lai,Kai Yan,Yichen Yang,Jun Yao,Wenjian Shen,Xin Zhang,Bin Li,Ying Liang,Yong Peng,Wangnan Li
标识
DOI:10.1093/bulcsj/uoaf018
摘要
Abstract Perovskite solar cells (PSCs) are currently recognized as the most competitive technologies in the photovoltaic industry. However, the power conversion efficiency (PCE) and stability of PSCs are significantly affected by various defects when synthesized via the antisolvent-free approach. Here, we report an effective defect passivation and perovskite crystal lattice regulation strategy by incorporating indium (III) chloride (InCl3) into the perovskite precursor solution. The smaller In3+ inserts interstitial sites and binds with the under-coordinated halide defects while releasing the micro strain of the perovskite lattice. Consequently, the long-lived carriers and higher quantum yield have been observed via the photoluminescence measurements. The incorporation of InCl3 significantly enhances the crystal structure stability under thermal, light, and moisture aging test conditions. Accordingly, the modified devices achieve a PCE of 24.43% on small-area modules and 21.19% on large-area modules (5 cm × 5 cm). The PCE of the InCl3-PSCs with an n–i–p planar structure maintains 80% initial efficiency after 378 h of maximum power point tracking.
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