钙钛矿(结构)
成核
纳米晶
光致发光
纳米线
卤化物
材料科学
模板
纳米技术
化学工程
配体(生物化学)
产量(工程)
结晶学
化学
无机化学
光电子学
有机化学
工程类
受体
生物化学
冶金
作者
Hanjun Yang,Tong Cai,Lacie Dube,Katie Hills‐Kimball,Ou Chen
标识
DOI:10.1021/acs.cgd.1c00118
摘要
The synthesis of lead-halide perovskite (LHP) thin nanowires (NWs) has been a challenging task that requires delicate control of nanocrystal (NC) nucleation and growth processes. Herein, we present a novel synthesis of ultrathin CsPbBr3 NWs through a postsynthetic transformation reaction starting from zero-dimensional Cs4PbBr6 perovskite NCs. The synthesized CsPbBr3 NWs averaged 2.5 nm in width and tens of micrometers in length, showing a blue photoluminescence with an emission quantum yield of 15.2%. Mechanistic studies show that the morphology of the final transformation product is determined by the chain length of the capping ligand and thus the formed template structure of the PbBr2-ligand intermediates. We demonstrate that this reaction scheme can be applied to the synthesis of CsPbI3 NCs with a low-dimensional morphology. Our study provides not only a new route to achieve ultrathin LHP NWs postsynthesis but also insights into the template-related nucleation and growth mechanisms of LHP NCs.
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