钙钛矿(结构)
卤化物
钝化
碘化物
材料科学
太阳能电池
沉积(地质)
薄膜
相(物质)
化学工程
金属
分析化学(期刊)
化学
无机化学
图层(电子)
纳米技术
光电子学
结晶学
有机化学
地质学
冶金
古生物学
沉积物
工程类
作者
Carlo A. R. Perini,Andrés‐Felipe Castro‐Méndez,Tim Kodalle,Magdalena Ravello,Juanita Hidalgo,Martín Gómez-Dominguez,Ruipeng Li,Margherita Taddei,Rajiv Giridharagopal,Justin Pothoof,Carolin M. Sutter‐Fella,David S. Ginger,Juan‐Pablo Correa‐Baena
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-02-15
卷期号:8 (3): 1408-1415
被引量:12
标识
DOI:10.1021/acsenergylett.2c02419
摘要
Interfacial passivation with bulky organic cations such as phenetylammonium iodide has enabled high performance for metal halide perovskite optoelectronic devices. However, the homogeneity of these interfaces and their formation dynamics are poorly understood. We study how Ruddlesden–Popper 2D phases form at a 3D perovskite interface when the 2D precursors are introduced via solution or via vapor. When using vapor deposition, we observe uniform coverage of the capping layer and the formation of a predominantly n = 2 Ruddlesden–Popper phase. In contrast, when using solution deposition, we observe the presence of a mixture of n = 2 and n = 1 in the film and the formation of aggregates of the organic cations. As a result of the better phase purity and uniformity, vapor deposition enables higher median solar cell performance with narrower distribution compared to solution-treated films. This study provides fundamental information that the perovskite community can use to better design capping layers to achieve higher charge extraction efficiencies.
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