卤化物
钙钛矿(结构)
甲脒
材料科学
碘化物
二甲基甲酰胺
金属
化学计量学
化学工程
溴化物
格式化
无机化学
化学
有机化学
催化作用
溶剂
工程类
作者
Benjia Dou,Lance M. Wheeler,Jeffrey A. Christians,David T. Moore,Steven P. Harvey,Joseph J. Berry,Frank S. Barnes,Sean E. Shaheen,Maikel F. A. M. van Hest
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-03-20
卷期号:3 (4): 979-985
被引量:91
标识
DOI:10.1021/acsenergylett.8b00305
摘要
Whereas the promise of metal halide perovskite (MHP) photovoltaics (PV) is that they can combine high efficiency with solution-processability, the chemistry occurring in precursor inks is largely unexplored. Herein, we investigate the degradation of MHP solutions based on the most widely used solvents, dimethylformamide (DMF) and dimethyl sulfoxide (DMSO). For the MHP inks studied, which contain formamidinium (FA+), methylammonium (MA+), cesium (Cs+), lead (Pb2+), bromide (Br–), and iodide (I–), dramatic compositional changes are observed following storage of the inks in nitrogen in the dark. We show that hydrolysis of DMF in the precursor solution forms dimethylammonium formate, which subsequently incorporates into the MHP film to compromise the ability of Cs+ and MA+ to stabilize FA+-based MHP. The changes in solution chemistry lead to a modification of the perovskite film stoichiometry, band gap, and structure. The solid precursor salts are stable when ball-milled into a powder, allowing for the storage of large quantities of stoichiometric precursor materials.
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