锡
钙钛矿(结构)
氟化物
材料科学
化学工程
工程物理
纳米技术
无机化学
化学
冶金
工程类
作者
Ziyu Tan,Hui Xiong,Min Wu,Songyang Yuan,Mengdi Zhan,Wenjian Yang,Jiandong Fan,Wenzhe Li
出处
期刊:Solar RRL
[Wiley]
日期:2024-01-19
卷期号:8 (5)
标识
DOI:10.1002/solr.202301024
摘要
In advancing high‐performance tin‐based perovskite solar cells, rapid crystallization and oxidation susceptibility are key challenges. SnF 2 , often added to control crystallization and oxidation, may impact cell performance, particularly postannealing. This study uses in situ variable‐temperature X‐Ray diffraction to examine SnF 2 's physicochemical behavior and phase transitions in these cells. The analysis highlights how residual SnF 2 affects carrier recombination through energy‐level structures. Postfilm formation, SnF 2 chemically interacts with 2,2′:6′,2″‐Terpyridine (TPY), forming a stannous fluoride complex that enhances electron transport and energy alignment. Crucially, TPY passivates surface defects and reduces tin vacancies, boosting device stability. The experimental results indicate that the unencapsulated devices in air atmosphere exhibit a stabilized power output retention rate above 90% of the initial efficiency after 29.5 h. After ≈800 h of continuous illumination in ambient air, the conversion efficiency can still be maintained above 100%. Remarkably, t 90 (time to retain 90% efficiency) of the target device in pure oxygen is over 24 h.
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