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原位实时研究金属卤化物钙钛矿薄膜的动态形成和转化过程。

In Situ Real-Time Study of the Dynamic Formation and Conversion Processes of Metal Halide Perovskite Films.

机构信息

School of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China.

Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201204, China.

出版信息

Adv Mater. 2018 Mar;30(11). doi: 10.1002/adma.201706401. Epub 2018 Jan 22.

Abstract

Metal halide perovskite solar cells (PSCs) have advanced to the forefront of solution-processed photovoltaic techniques and made stunning progress in power conversion efficiency (PCE). Further improvements in device performances rely on perfecting the structure and morphology of perovskite films. However, undesirable defects such as pinholes and grain boundaries are often created in film preparations due to lack of knowledge of the precise reaction mechanism. Here, in situ grazing-incidence X-ray diffraction (GI-XRD) investigations are performed, facilitated by other techniques, on the formation of the widely adopted MAPbI (MA = methylammonium) perovskite films from their intermediate adduct (IA) phases. The influences of solvent vapor atmospheres on MAPbI films are also systematically investigated, where the dynamic conversion processes between different phases are visualized in real time. Further in situ GI-XRD and infrared spectroscopy measurements reveal that the IA phases contain both N,N-dimethylformamide and dimethyl sulfoxide (DMSO) as coordinating molecules. By tuning the DMSO concentration in perovskite precursors, the ideal perovskite film is formed and the best PCE is achieved for the planar MAPbI -based PSCs. These findings highlight the role of IA phases and the effect of solvent atmospheres on the quality of perovskite films, providing direct insights into their growth mechanism.

摘要

金属卤化物钙钛矿太阳能电池(PSCs)已经成为溶液处理光伏技术的前沿,并在功率转换效率(PCE)方面取得了惊人的进展。进一步提高器件性能依赖于完善钙钛矿薄膜的结构和形态。然而,由于对精确反应机制的了解不足,在薄膜制备过程中经常会产生不理想的缺陷,如针孔和晶界。在这里,通过其他技术辅助,我们对广泛采用的 MAPbI(MA = 甲基铵)钙钛矿薄膜从其中间加合物(IA)相的形成进行了原位掠入射 X 射线衍射(GI-XRD)研究。我们还系统地研究了溶剂蒸汽气氛对 MAPbI 薄膜的影响,实时观察了不同相之间的动态转换过程。进一步的原位 GI-XRD 和红外光谱测量表明,IA 相含有 N,N-二甲基甲酰胺和二甲基亚砜(DMSO)作为配位分子。通过调整钙钛矿前驱体中的 DMSO 浓度,可以形成理想的钙钛矿薄膜,并为基于平面 MAPbI 的 PSCs 实现最佳的 PCE。这些发现强调了 IA 相的作用以及溶剂气氛对钙钛矿薄膜质量的影响,为它们的生长机制提供了直接的见解。

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