钙钛矿(结构)
成核
材料科学
结晶
化学工程
能量转换效率
图层(电子)
钙钛矿太阳能电池
纳米技术
化学
有机化学
光电子学
工程类
作者
Jianjun Zhang,Liuyang Zhang,Xiaohe Li,Xinyi Zhu,Jiaguo Yu,Ke Fan
标识
DOI:10.1021/acssuschemeng.8b05734
摘要
Two-dimensional (2D) organic–inorganic hybrid perovskite materials have recently attracted tremendous attention for use in perovskite solar cells (PSCs) by virtue of their considerable long-term stability. However, the primary stumbling block for their application in PSC is their relatively lower power conversion efficiency (PCE) compared with the conventional 3D perovskite. In this work, through a binary solvent engineering of dimethylformamide (DMF)/dimethyl sulfoxide (DMSO) in the precursor solution, high-performance 2D perovskite planar solar cells are fabricated with beyond 10% PCE and outstanding environmental stability. In the formation of the 2D perovskite film during the hot-coating process, heterogeneous nucleation primarily occurs at the air–liquid interface, contributing to the formation of the thin, flaky cap layer on the outmost surface of the film. Sequentially, for the unary solvent DMF, its fast volatilization facilitates homogeneous nucleation, resulting in random-orientated perovskite grains in the inner layer. In contrast, with the binary solvent engineering of DMF/DMSO, the formation of intermediate can slow the crystallization process, making the perovskite cap layer serve as the seed that impels the subsequent perovskite crystallization to be vertically orientated in the inner layer of the perovskite film. These findings provide not only a new understanding of the 2D perovskite crystallization process but also a simple and effective method to fabricate high-performance 2D perovskite-based photovoltaics.
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