钙钛矿(结构)
材料科学
光伏系统
串联
卤化物
光电子学
X射线光电子能谱
光致发光
光伏
相(物质)
再分配(选举)
电荷(物理)
最大功率点跟踪
离子键合
纳米技术
跟踪(教育)
理论(学习稳定性)
化学工程
化学物理
三碘化物
最大功率原理
光谱学
太阳能电池
作者
Seongheon Kim,G Y Kim,Taegeon Kim,Kwang Seop Shin,Junsu Kim,M. Y. Choi,Yun Seog Lee,Namyoung Ahn
摘要
ABSTRACT Mixed‐halide wide‐bandgap (WBG) perovskites with bandgaps above 1.65 eV are essential top‐cell absorbers for tandem photovoltaics. However, bromide‐rich WBG perovskites suffer from photo‐induced halide segregation, while its origin under operating conditions remains unclear. Here, we identify trapped‐charge accumulation as a key factor triggering phase segregation during operation and develop a practical operational strategy to mitigate this process. Time‐evolving photoluminescence and depth‐profiling x‐ray photoelectron spectroscopy reveal that trapped‐charge accumulation accelerates ionic redistribution and halide segregation under illumination. Based on this insight, we introduce a maximum stability point tracking (MSPT) strategy that periodically relieves charge accumulation during device operation. WBG perovskite solar cells (PSCs) operated under MSPT retain approximately 90% of their initial power after 700 h of continuous operation, whereas devices operated under conventional maximum power point tracking (MPPT) rapidly degrade during the early stages of operation. Post‐operational analyses further reveal that MSPT preserves the alloyed perovskite phase, whereas MPPT induces pronounced phase segregation. As an operation‐stage strategy that mitigates charge accumulation without altering material composition, MSPT is compatible with existing material approaches and offers a route toward more stable perovskite photovoltaics. These findings provide an operational guideline for stabilizing WBG PSCs and advancing tandem photovoltaic technologies.
科研通智能强力驱动
Strongly Powered by AbleSci AI