降级(电信)
材料科学
钙钛矿(结构)
卤化物
离子
开路电压
屏蔽效应
电场
电压
化学物理
光电子学
化学
无机化学
物理
工程类
电子工程
凝聚态物理
结晶学
量子力学
有机化学
作者
Jarla Thiesbrummel,Sahil Shah,Emilio Gutierrez‐Partida,Fengshuo Zu,Francisco Peña‐Camargo,Stefan Zeiske,Jonas Diekmann,Fangyuan Ye,Karol Pawel Peters,Kai Oliver Brinkmann,Pietro Caprioglio,Akash Dasgupta,Seongrok Seo,Fatai A. Adeleye,Jonathan Warby,Quentin Jeangros,Felix Lang,Shuo Zhang,Steve Albrecht,Thomas Riedl
出处
期刊:Nature Energy
[Nature Portfolio]
日期:2024-03-28
卷期号:9 (6): 664-676
被引量:67
标识
DOI:10.1038/s41560-024-01487-w
摘要
Abstract The presence of mobile ions in metal halide perovskites has been shown to adversely affect the intrinsic stability of perovskite solar cells (PSCs). However, the actual contribution of mobile ions to the total degradation loss compared with other factors such as trap-assisted recombination remains poorly understood. Here we reveal that mobile ion-induced internal field screening is the dominant factor in the degradation of PSCs under operational conditions. The increased field screening leads to a decrease in the steady-state efficiency, often owing to a large reduction in the current density. Instead, the efficiency at high scan speeds (>1,000 V s −1 ), where the ions are immobilized, is much less affected. We also show that the bulk and interface quality do not degrade upon ageing, yet the open-circuit voltage decreases owing to an increase in the mobile ion density. This work reveals the importance of ionic losses for intrinsic PSC degradation before chemical or extrinsic mechanical effects manifest.
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