钙钛矿(结构)
结晶
成核
材料科学
化学工程
Crystal(编程语言)
晶体生长
能量转换效率
相(物质)
光电子学
结晶学
化学
有机化学
计算机科学
工程类
程序设计语言
作者
Jian Qiu,Yingdong Xia,Yiting Zheng,Wei Hui,Hao Gu,Wenbo Yuan,Hui Yu,Lingfeng Chao,Tingting Niu,Yingguo Yang,Xingyu Gao,Yonghua Chen,Wei Huang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-06-05
卷期号:4 (7): 1513-1520
被引量:193
标识
DOI:10.1021/acsenergylett.9b00954
摘要
2D Ruddlesden–Popper (2DRP) tin (Sn) perovskite solar cells (PSCs) play an irreplaceable role in advancing the commercialization of perovskite-based photovoltaic devices due to their low toxicity and improved stability. However, the efficiency of 2DRP Sn PSCs has not made a breakthrough owing to incompletely oriented crystal growth and poor film morphology, which is limited by a complex and uncontrollable crystallization process. Here, we first introduce the mixed spacer organic cations [n-butylamine (BA) and phenylethylamine (PEA)] in 2DRP Sn perovskite to control the crystallization process. We find that when the BA+ and PEA+ co-work to form [(BA0.5PEA0.5)2FA3Sn4I13] 2DRP perovskites, the intermediate phase impeding the homogeneous and ordered nucleation of the crystal is suppressed effectively, thus enabling a high-quality film morphology and improved crystal orientation. Benefitting from it, the power conversion efficiency (PCE) is improved to 8.82%, which is the highest one among the 2DRP Sn PSCs as far as we known.
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