纳米棒
正交晶系
纳米晶
成核
材料科学
各向异性
钙钛矿(结构)
八面体
格子(音乐)
离子
纳米技术
卤化物
凝聚态物理
结晶学
化学物理
晶体结构
化学
无机化学
光学
物理
有机化学
声学
作者
Biswajit Hudait,Sumit Kumar Dutta,Suman Bera,Narayan Pradhan
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-06-01
卷期号:21 (12): 5277-5284
被引量:27
标识
DOI:10.1021/acs.nanolett.1c01398
摘要
Lead halide perovskite nanocrystals, whether formed by their own nucleation and growth or by ion diffusion into the lattice of others, are still under investigation. Moreover, beyond isotropic nanocrystals, fabricating anisotropic perovskite nanocrystals by design has remained difficult. Exploring the lattice of orthorhombic-phase Cs2ZnBr4 with the complete replacement of Zn tetrahedra by Pb octahedra, dimension-tunable anisotropic nanocrystals of CsPbBr3 are reported. This B-site ion introduction led to CsPbBr3 nanorods having [100] as major axis, in contrast with all reports on rods/wires where the lengths were along the [001] direction. This was possible by using derivatives of α-bromo ketones, which helped in tuning the shape of Cs2ZnBr4 and also the facets of transformed CsPbBr3. While similar experiments are extended to orthorhombic Cs2HgBr4, standard nanorods with [001] as the major axis were observed. From these results, it is further concluded that anisotropic perovskite nanocrystals might not follow any specific rules for directional growth and instead might depend on the structure of the parent lattice.
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