卤化物
八面体
超分子化学
化学
钙钛矿(结构)
结晶学
碱金属
离子键合
晶体工程
格子(音乐)
块(置换群论)
晶体结构
金属
纳米技术
离子
无机化学
材料科学
几何学
有机化学
物理
数学
声学
作者
Cheng Zhu,Jianbo Jin,Mengyu Gao,Alexander M. Oddo,Maria C. Folgueras,Ye Zhang,Chung-Kuan Lin,Peidong Yang
摘要
The structural diversity and tunable optoelectronic properties of halide perovskites originate from the rich chemistry of the metal halide ionic octahedron [MX6]n- (M = Pb2+, Sb3+, Te4+, Sn4+, Pt4+, etc.; X = Cl-, Br-, and I-). The properties of the extended perovskite solids are dictated by the assembly, connectivity, and interaction of these octahedra within the lattice environment. Hence, the ability to manipulate and control the assembly of the octahedral building blocks is paramount for constructing new perovskite materials. Here, we propose a systematic supramolecular strategy for the assembly of [MX6]n- octahedra into a solid extended network. Interaction of alkali metal-bound crown ethers with the [M(IV)X6]2- octahedron resulted in a structurally and optoelectronically tunable "dumbbell" structural unit in solution. Single crystals with diverse packing geometries and symmetries will form as the solid assembly of this new supramolecular building block. This supramolecular assembly route introduces a new general strategy for designing halide perovskite structures with potentially new optoelectronic properties.
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