钙钛矿(结构)
成核
卤化物
材料科学
图层(电子)
铯
表征(材料科学)
钙钛矿太阳能电池
纳米技术
原位
能量转换效率
化学工程
化学物理
光活性层
光伏系统
化学
作者
Keonwoo Park,Dongbo Zhang,Do-Kyoung Lee,Tim Kodalle,Dongjun Lee,Joo‐Hong Lee,Joo-Hong Lee,Seung‐Gu Choi,Ga‐Yeong Kim,Jae-Hwan Kim,Gwanghee Lee,Ji‐Sang Park,Carolin M. Sutter‐Fella,Jin-Wook Lee,Jin-Wook Lee
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-12-15
卷期号:11 (1): 548-556
被引量:1
标识
DOI:10.1021/acsenergylett.5c03152
摘要
Over the recent few years, extensive research efforts have shifted from normal (n-i-p) to inverted (p-i-n) perovskite solar cells (PSCs), owing to their promising efficiency and operational stability, enabled by low-temperature processing. Despite a fundamentally identical operation principle (only structurally inverted), the optimized perovskite compositions for normal and inverted PSCs differ significantly across the literature, suggesting an underlying design principle for perovskite composition. Here, we unveil the role of cesium cation in enhancing interfacial contact between the perovskite layer and the underlying hole-transporting layer (HTL) in inverted PSCs. Comprehensive in situ and device characterization reveal that cesium incorporation promotes the formation of initial nucleation seeds for heterogeneous nucleation at the perovskite/hydrophobic HTL interface, thereby improving their contact. The resulting compositional heterogeneity explains the focus of recent studies on resolving this issue. This study provides mechanistic insight into designing perovskite compositions to further enhance the performance and longevity of PSCs.
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