Wang Sasa, Liu Xitao, Li Lina, Ji Chengmin, Sun Zhihua, Wu Zhenyue, Hong Maochun, Luo Junhua
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter , Chinese Academy of Sciences , Fuzhou 350002 , China.
University of Chinese Academy of Sciences , Beijing 100049 , China.
J Am Chem Soc. 2019 May 15;141(19):7693-7697. doi: 10.1021/jacs.9b02558. Epub 2019 May 7.
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, EAPbBr (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.
多轴分子铁电体中,自发极化的多方向切换产生了多样的性质,展现出许多引人入胜的优势,使其成为传统无机氧化物不可或缺的补充。尽管近来取得了蓬勃进展,但具有体光伏效应的多轴分子铁电体仍存在巨大空白。在此,我们报道一种双轴卤化铅铁电体EAPbBr(1,EA = 乙铵),它采用独特的三层钙钛矿结构,居里温度高达约384 K。特别地,对于1,4/mmmFmm2物种的明显对称性破缺导致在铁电相中出现四个等效极化方向。基于其双轴性质,1的体光伏效应可通过电极化在这些多方向之间轻松调节。据我们所知,这是关于双轴杂化钙钛矿铁电体显示方向可调光伏活性的首次报道。这项工作为控制多轴分子铁电体的体物理性质提供了一条途径,并突出了它们在智能设备领域进一步应用的潜力。