铁电性
极化
居里温度
钙钛矿(结构)
极化(电化学)
光伏系统
卤化物
材料科学
电场
化学
光电子学
化学物理
纳米技术
凝聚态物理
电介质
结晶学
物理
物理化学
电气工程
无机化学
工程类
铁磁性
量子力学
作者
Sasa Wang,Xitao Liu,Lina Li,Chengmin Ji,Zhihua Sun,Zhenyue Wu,Maochun Hong,Junhua Luo
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, EA4Pb3Br10 (1, EA = ethylammonium), which adopts the unique trilayered perovskite motif with a high Curie temperature of ∼384 K. Particularly, for 1, the distinct symmetry breaking with 4/ mmmF mm2 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI