Three-Dimensional Lead Bromide Hybrid Ferroelectric Realized by Lattice Expansion

卤化物 化学 八面体 钙钛矿(结构) 铁电性 居里温度 电介质 溴化物 结晶学 晶体结构 化学物理 无机化学 凝聚态物理 光电子学 材料科学 物理 铁磁性
作者
Yuan‐Yuan Tang,Yuhua Liu,Hang Peng,Bin‐Bin Deng,Tingting Cheng,Yanting Hu
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:142 (46): 19698-19704 被引量:50
标识
DOI:10.1021/jacs.0c09586
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 (Tc) 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 Tc 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.
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