卤化物
甲脒
碱金属
钙钛矿(结构)
带隙
光致发光
相(物质)
材料科学
光电子学
碘化物
能量转换效率
无机化学
化学
有机化学
结晶学
作者
Xin Meng,Jianan Wang,Haixin Wang,Mengjie Li,Derun Sun,Xiao Hu,Jizhou He,Yu Peng,Jing Zhou,Rui Chen,Fumeng Ren,Sanwan Liu,Shasha Zhang,Yiqiang Zhang,Zhao Zhi-guo,Zonghao Liu,Wei Chen
出处
期刊:Solar RRL
[Wiley]
日期:2023-01-06
卷期号:7 (5)
被引量:17
标识
DOI:10.1002/solr.202201099
摘要
Wide‐bandgap perovskites have attracted much attention due to their potential application in perovskite‐based tandem solar cells, which can surpass the theoretical efficiency up‐limit of single‐junction solar cells. However, photoinduced phase segregation remains one of the most intractable impediments that deteriorate the operational stability of wide‐bandgap perovskites solar cells. Herein, the effect of a series of alkali halides additives on the photoinduced phase segregation of wide‐bandgap perovskites with the composition of FA 0.8 Cs 0.2 Pb(I 0.7 Br 0.3 ) 3 (FA is formamidinium) is systematically studied. By coupling in situ time‐dependent photoluminescence technique, potassium chloride (KCl) is demonstrated to be the best in suppressing the photoinduced phase segregation. The reduced iodine vacancy defects owing to supplemented chloride ions and the coupling of potassium ions with the accumulated iodide ions at the grain boundaries lead to effective suppression phase segregation. As a consequence, the KCl‐modified wide‐bandgap perovskite solar cells present a champion efficiency of 19.34%, and the devices can maintain 93% of the initial efficiency after light soaking for 500 h with maximum power point tracking under 1 sun equivalent white light‐emitting diode illumination, much superior to the reference device without KCl modification only retaining 72% of its initial efficiency.
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