Effects of Solvent Coordination Strength on the Morphology of Solution-Processed BiI3 Thin Films

被引:15
作者
Hamdeh, Umar H. [1 ]
Nelson, Rainie D. [1 ]
Ryan, Bradley J. [1 ]
Panthani, Matthew G. [1 ]
机构
[1] Iowa State Univ, Dept Chem & Biol Engn, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
METHYLAMMONIUM BISMUTH IODIDE; METAL-HALIDE PEROVSKITES; OPEN-CIRCUIT VOLTAGE; LEAD-FREE; SOLAR-CELLS; DEGRADATION; PERFORMANCE; TRIHALIDE; BIL(3);
D O I
10.1021/acs.jpcc.9b00481
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The remarkable performance of Pb halide perovskites in optoelectronic devices is complicated by concerns over their toxicity, which has motivated a search for Pb-free alternatives that have similar performance. Bi halides and halide perovskites have been predicted to be among the most promising Pb-free alternatives; however, their performance in devices has fallen short of expectations. One of the major challenges in fabricating efficient devices based on these Bi-based alternatives has been poor control over the morphology of thin films. Using BiI3 as a model system, we demonstrate that the film morphology and surface coverage are strongly dependent on the Lewis basicity of solvents that are used during deposition. We demonstrate that coordinating BiI3 with strong Lewis bases in tetrahydrofuran results in conformal films that have been difficult to achieve using conventional deposition techniques.
引用
收藏
页码:13394 / 13400
页数:7
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