甲脒
材料科学
钝化
无定形固体
钙钛矿(结构)
碘化物
成核
能量转换效率
十八烷基三氯氢硅
化学工程
范德瓦尔斯力
卤化物
相(物质)
位阻效应
结晶度
铯
碘化氢
结晶
三碘化物
三卤化物
同质性(统计学)
化学物理
咔唑
接受者
作者
Kaibo Zhao,Rongshan Zhuang,Anxin Sun,Congcong Tian,Y ZHAO,Ran Li,Tiantian Cen,Teng Xue,Qianwen Chen,Hanfa Ni,Shuhang Chen,Tianrui Zhao,C J Chen
摘要
ABSTRACT Formamidinium‐cesium lead iodide (FACsPbI 3 ) perovskites with methylammonium‐free compositions have demonstrated improved intrinsic stability and hold promise for the commercialization of perovskite solar cells (PSCs). However, phase inhomogeneity caused by the segregation of A‐site cations limits further improvements in device efficiency. In this work, a self‐assembled molecule (4‐(3,6‐bis(1,3‐benzodioxole‐5‐yl)‐9H‐carbazole‐9‐yl)butyl)phosphonic acid (PhDo4PACz) was designed by introducing a benzodioxole group into the carbazole unit. The benzodioxole group provides additional steric hindrance and non‐coplanar van der Waals interactions, forming an amorphous self‐assembled multilayer on the substrate. Additionally, there is a strong intermolecular interaction between the benzodioxole group and FA + , which reduces the nucleation barrier and anchors FA at the bottom of the perovskite. Consequently, the perovskite film deposited on this self‐assembled multilayer exhibits improved phase homogeneity. Furthermore, PhDo4PACz enhances energy level alignment and defect passivation at the buried interface, resulting in minimized bandgap‐to‐voltage loss (0.091 eV) and maximized fill factor (86.10%). As a result, inverted PSCs based on PhDo4PACz/FTO substrates achieved a champion power conversion efficiency (PCE) of 26.75% (certified 26.27% for reverse‐scan), retaining 95.15% of their initial efficiency after 1500 h of illumination under the ISOS‐L‐2 protocol, demonstrating great potential for excellent stability and industrial applications.
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