Three-Dimensional Lead Bromide Hybrid Ferroelectric Realized by Lattice Expansion

被引:43
|
作者
Tang, Yuan-Yuan [1 ]
Liu, Yu-Hua [1 ]
Peng, Hang [1 ]
Deng, Bin-Bin [1 ]
Cheng, Ting-Ting [1 ]
Hu, Yan-Ting [1 ]
机构
[1] Nanchang Univ, Ordered Matter Sci Res Ctr, Nanchang 330031, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
MOLECULAR PEROVSKITE; HALIDE PEROVSKITES; TEMPERATURE; CRYSTALS;
D O I
10.1021/jacs.0c09586
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three-dimensional (3D) organic-inorganic lead halide hybrids have become a hot academic topic because of their various functional properties. However, 3D lead halide hybrid ferroelectrics are still very rare until now. Here, we report a new 3D lead halide perovskite-related ferroelectric, (EATMP)Pb2Br6 [EATMP = (2-aminoethyl)-trimethylphosphanium]. Based on nonferroelectric CH3NH3PbBr3, by replacing PbBr6 octahedra with a Pb2Br10 dimer of edge-sharing octahedra as the basic building unit, the expanded 3D lead bromide perovskite analog was formed with the large [EATMP](2+) cations occupying the voids of framework. Notably, (EATMP)Pb2Br6 displays a direct bandgap of 2.81 eV, four polarization directions, and a high Curie temperature (T-c) of 518 K (much beyond that of BaTiO3, 393 K), which is the highest among all reported 3D organic-inorganic hybrid ferroelectrics. Such a high T-c may result from the high rotational energy barrier of cations induced by a larger molecular volume and relatively low crystal symmetry. Our work provides an efficient avenue to construct new 3D organic-inorganic lead halide hybrids and would inspire the further exploration of 3D lead halide ferroelectrics.
引用
收藏
页码:19698 / 19704
页数:7
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