Ferroelectricity of the Orthorhombic and Tetragonal MAPbBr3 Single Crystal

被引:42
|
作者
Gao, Zhang-Ran [1 ,2 ]
Sun, Xiao-Fan [1 ,2 ]
Wu, Yu-Ying [1 ,2 ]
Wu, Yi-Zhang [1 ,2 ]
Cai, Hong-Ling [1 ,2 ]
Wu, X. S. [1 ,2 ]
机构
[1] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Phys, Nanjing 210093, Jiangsu, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2019年 / 10卷 / 10期
关键词
HALIDE PEROVSKITES; HYBRID PEROVSKITE; HIGH-PERFORMANCE; CH3NH3PBI3; DISORDER;
D O I
10.1021/acs.jpclett.9b00776
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hybrid organic-inorganic halide perovskites (HOIPs) MAPbBr(3) and their ramifications have emerged because of the photovoltaic, optical, and other fascinating performances of HOIPs in recent years. However, many intrinsic properties, such as crystal structure and ferroelectricity, are still controversial. In this work, the ferroelectricity of the orthorhombic and tetragonal MAPbBr(3) single crystal was confirmed through the dielectric behavior versus bias electric field epsilon(E), the temperature-dependent pyroelectric current with positive/negative poling, and the positive-up-negative-down (PUND) measurements. The electric field dependence of dielectric constant curves shows a butterfly type shape in the orthorhombic and tetragonal phase. The pyroelectric current shows two maxima at 155 and 245 K, corresponding to ferroelectric-ferroelectric and ferroelectric-paraelectric phase transitions, respectively. In particular, the direction of the pyroelectric current can be reversed by a positive or negative poling electric field, which is the assertive evidence of ferroelectricity. The PUND measurements act as the most convincing proof of the ferroelectricity of the MAPbBr(3) single crystal. This work reports new evidence of the ferroelectric properties of the MAPbBr(3) single crystal, which provides the intrinsic property when considering their high power conversion efficiencies.
引用
收藏
页码:2522 / +
页数:11
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