材料科学
钙钛矿(结构)
基质(水族馆)
兴奋剂
钝化
能量转换效率
相(物质)
化学工程
薄膜
结晶
光电子学
纳米技术
图层(电子)
化学
海洋学
有机化学
工程类
地质学
作者
Fei Zheng,Chuantian Zuo,Meng-Si Niu,Chunhua Zhou,Siobhan J. Bradley,Christopher R. Hall,Wei-Long Xu,Xiaoming Wen,Xiaotao Hao,Mei Gao,Trevor A. Smith,Kenneth P. Ghiggino
标识
DOI:10.1021/acsami.0c05714
摘要
Layered perovskite films, composed of two-dimensional (2D) Ruddlesden–Popper perovskites (RPPs), show improved stability compared to their conventional three-dimensional (3D) counterparts in perovskite solar cells (PSCs). However, 2D PSCs exhibit a lower power conversion efficiency (PCE), which has been attributed to compositional inhomogeneity and nonuniform alignment of the 2D perovskite phases. Methylammonium chloride (MACl) has been adopted as an additive to improve the PCE and the operational stability of 2D PSCs, although the role of MACl in performance enhancement is unclear. In this work, time- and spatially resolved fluorescence and absorption techniques have been applied to study the composition and charge carrier dynamics in MACl-doped BA2MA4Pb5I16 (⟨n⟩ = 5) layered perovskite films. The inhomogeneous phase orientation distribution in the direction orthogonal to the substrate for undoped layered perovskite films undergoes reorganization upon MACl doping. Based on structural and crystallographic analyses, it is revealed that MACl can facilitate the crystallization of small-n 2D perovskite phases at the cost of consuming an increased amount of BA cations. Consequently, an increase in the thickness of large-n 2D perovskite phases accompanies their enhanced perpendicular alignment ([101] crystalline orientation) to the substrate, which facilitates charge carrier transport and collection by electrodes. The defect passivation of the MACl-doped layered perovskite film provided by the small-n phase is also beneficial to the photovoltaic performance of the PSC device. A maximum PCE (∼14.3%) was achieved at 6 mol % MACl doping, with this optimum level influenced by the increased interfacial roughness of the layered perovskite film caused by the edges of small-n perovskite flakes emerging on the front surface.
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