钙钛矿(结构)
材料科学
异质结
钝化
磁滞
化学计量学
能量转换效率
溶解过程
钙钛矿太阳能电池
相(物质)
化学工程
图层(电子)
光电子学
纳米技术
物理化学
凝聚态物理
化学
有机化学
工程类
物理
作者
M. C. Shih,Shaun Tan,Yongli Lu,Tim Kodalle,Do Kyung Lee,Yifan Dong,Bryon W. Larson,So Yeon Park,Ruiqi Zhang,Matthias J. Grotevent,Tara Šverko,Hua Zhu,Yu‐Kuan Lin,Carolin M. Sutter‐Fella,Kai Zhu,Matthew C. Beard,Vladimir Bulović,Moungi G. Bawendi
标识
DOI:10.1002/adma.202416672
摘要
Abstract Interface engineering plays a critical role in advancing the performance of perovskite solar cells. As such, 2D/3D perovskite heterostructures are of particular interest due to their optoelectrical properties and their further potential improvements. However, for conventional solution‐processed 2D perovskites grown on an underlying 3D perovskite, the reaction stoichiometry is normally unbalanced with excess precursors. Moreover, the formed 2D perovskite is impure, leading to unfavorable energy band alignment at the interface. Here a simple method is presented that solves both issues simultaneously. The 2D formation reaction is taken first to completion, fully consuming excess PbI 2 . Then, isopropanol is utilized to remove excess organic ligands, control the 2D perovskite thickness, and obtain a phase‐pure, n = 2, 2D perovskite. The outcome is a pristine (without residual 2D precursors) and phase‐pure 2D perovskite heterostructure with improved surface passivation and charge carrier extraction compared to the conventional solution process. PSCs incorporating this treatment demonstrate a notable improvement in both stability and power conversion efficiency, with negligible hysteresis, compared to the conventional process.
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