An Unprecedented Biaxial Trilayered Hybrid Perovskite Ferroelectric with Directionally Tunable Photovoltaic Effects

被引:168
作者
Wang, Sasa [1 ,2 ]
Liu, Xitao [1 ]
Li, Lina [1 ]
Ji, Chengmin [1 ]
Sun, Zhihua [1 ]
Wu, Zhenyue [1 ,2 ]
Hong, Maochun [1 ]
Luo, Junhua [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
THIN-FILM; HALIDE; TEMPERATURE;
D O I
10.1021/jacs.9b02558
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multiaxial molecular ferroelectrics, in which multiple-directional switching of spontaneous polarization creates diverse properties, have shown many intriguing advantages, making them indispensable complements to conventional inorganic oxides. Despite recent blooming advances, multiaxial molecular ferroelectric with bulk photovoltaic effects still remains a huge blank. Herein, we report a biaxial lead halide ferroelectric, EA(4)Pb(3)Br(10) (1, EA = ethylammonium), which adopts the unique trilayered perovskite motif with a high Curie temperature of similar to 384 K. Particularly, for 1, the distinct symmetry breaking with 4/mmmFmm2 species leads to the emergence of four equivalent polarization directions in the ferroelectric phase. Based on its biaxial nature, the bulk photovoltaic effect of 1 can be facilely tuned between such multiple directions through electric poling. As far as we know, this is the first report on biaxial hybrid perovskite ferroelectric showing directionally tunable photovoltaic activity. This work provides an avenue to control the bulk physical properties of multiaxial molecular ferroelectrics, and highlights their potential for further applications in the field of smart devices.
引用
收藏
页码:7693 / 7697
页数:5
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