钙钛矿(结构)
溴化物
极性(国际关系)
材料科学
铯
卤化物
氯仿
正交晶系
己烷
氯化物
化学
纳米晶
溶剂
无机化学
纳米技术
晶体结构
结晶学
有机化学
细胞
生物化学
作者
Anirban Dutta,Rakesh Kumar Behera,Narayan Pradhan
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-03-21
卷期号:4 (4): 926-932
被引量:61
标识
DOI:10.1021/acsenergylett.9b00443
摘要
A minute difference in solvent polarity of hydrophobic solvents can drastically alter the rate of formation of cesium lead halide perovskite nanocrystals. This has been observed at room temperature and in single-solvent synthesis routes for cesium lead bromide and cesium lead chloride nanocrystals. Through the exploration Pb-thiolate as the active precursor and using seven different hydrophobic solvents, the polarity of which varied from chloroform to hexane, the phase of cesium lead bromide changed from orthorhombic-CsPbBr3 to trigonal-Cs4PbBr6. In contrast, for cesium lead chloride, the phase remained cubic-CsPbCl3 in all solvents, but their shape turned from cube to platelet. Because the rate of the reaction was controlled here, doping of Mn(II) was performed for all cases, and efficient doping was observed for the slower reaction in the hexane medium. The reaction chemistry and the physical processes associated with these formation processes were systematically analyzed and are reported in this Letter.
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