材料科学
降级(电信)
碘化物
钙钛矿(结构)
图层(电子)
卤化物
阳极
阴极
光电子学
太阳能电池
化学物理
化学工程
钙钛矿太阳能电池
化学
无机化学
纳米技术
电极
结晶学
物理化学
工程类
电信
计算机科学
作者
Zhenyi Ni,Haoyang Jiao,Chengbin Fei,Hangyu Gu,Shuang Xu,Zhenhua Yu,Guang Yang,Yehao Deng,Qi Jiang,Ye Liu,Yanfa Yan,Jinsong Huang
出处
期刊:Nature Energy
[Springer Nature]
日期:2021-12-22
卷期号:7 (1): 65-73
被引量:207
标识
DOI:10.1038/s41560-021-00949-9
摘要
The efficiency and stability of perovskite solar cells are essentially determined by defects in the perovskite layer, yet their chemical nature and linking with the degradation mechanism of devices remain unclear. Here we uncover where degradation occurs and the underlying mechanisms and defects involved in the performance degradation of p–i–n perovskite solar cells under illumination or reverse bias. Light-induced degradation starts with the generation of iodide interstitials at the interfacial region between the perovskite and both charge transport layers. While we observe trap annihilation of two types of iodide defect at the anode side, we find negatively charged iodide interstitials near the cathode side, which we show to be more detrimental to the solar cell efficiency. The reverse-bias degradation is initialized by the interaction between iodide interstitials and injected holes at the interface between the electron transport layer and the perovskite. Introducing a hole-blocking layer between the layers suppresses this interaction, improving the reverse-bias stability.
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