Zhang Ye, Parsonnet Eric, Fernandez Abel, Griffin Sinéad M, Huyan Huaixun, Lin Chung-Kuan, Lei Teng, Jin Jianbo, Barnard Edward S, Raja Archana, Behera Piush, Pan Xiaoqing, Ramesh Ramamoorthy, Yang Peidong
Department of Chemistry, University of California, Berkeley, CA 94720, USA.
Department of Physics, University of California, Berkeley, CA 94720, USA.
Sci Adv. 2022 Feb 11;8(6):eabj5881. doi: 10.1126/sciadv.abj5881. Epub 2022 Feb 9.
Ferroelectric semiconductors are rare materials with both spontaneous polarizations and visible light absorptions that are promising for designing functional photoferroelectrics, such as optical switches and ferroelectric photovoltaics. The emerging halide perovskites with remarkable semiconducting properties also have the potential of being ferroelectric, yet the evidence of robust ferroelectricity in the typical three-dimensional hybrid halide perovskites has been elusive. Here, we report on the investigation of ferroelectricity in all-inorganic halide perovskites, CsGeX, with bandgaps of 1.6 to 3.3 eV. Their ferroelectricity originates from the lone pair stereochemical activity in Ge (II) that promotes the ion displacement. This gives rise to their spontaneous polarizations of ~10 to 20 μC/cm, evidenced by both ab initio calculations and key experiments including atomic-level ionic displacement vector mapping and ferroelectric hysteresis loop measurement. Furthermore, characteristic ferroelectric domain patterns on the well-defined CsGeBr nanoplates are imaged with both piezo-response force microscopy and nonlinear optical microscopic method.
铁电半导体是一种稀有材料,兼具自发极化和可见光吸收特性,有望用于设计功能光铁电体,如光开关和铁电光电池。新兴的卤化物钙钛矿具有显著的半导体特性,也有成为铁电体的潜力,但典型三维混合卤化物钙钛矿中强铁电性的证据一直难以捉摸。在此,我们报告了对带隙为1.6至3.3 eV的全无机卤化物钙钛矿CsGeX中铁电性的研究。它们的铁电性源于Ge(II)中的孤对立体化学活性,这种活性促进了离子位移。这导致它们的自发极化约为10至20 μC/cm²,这一结果通过从头算计算以及包括原子级离子位移矢量映射和铁电滞回环测量在内的关键实验得到了证实。此外,利用压电响应力显微镜和非线性光学显微镜方法对明确的CsGeBr纳米板上的特征铁电畴图案进行了成像。