甲脒
化学
铁电性
偶极子
光致发光
钙钛矿(结构)
化学物理
卤化物
碘化物
极地的
凝聚态物理
结晶学
光电子学
无机化学
电介质
材料科学
物理
有机化学
天文
作者
Willa Mihalyi‐Koch,Zhenbang Dai,Meng‐Jia Sun,Jae Yong Park,David P. Lafayette,Kyana M. Sanders,Ilia A. Guzei,John C. Wright,Libai Huang,Andrew M. Rappe,Song Jin
摘要
Ferroelectric Rashba semiconductors are a rare class of multifunctional materials promising for spin-orbitronics due to the possibility of electrically switchable spin textures. Hybrid organic-inorganic metal halide perovskites offer exceptional tunability that can be harnessed to target noncentrosymmetry; however, the complex interactions between organic and inorganic components are not rationally understood. Here, we use an asymmetric spacer cation with a strong molecular dipole moment (2-fluorobenzylammonium, 2FBZ) and increase the intrinsic quantum well thickness to n > 1 to synthesize three new polar 2D lead iodide perovskites (2FBZ)2(A)n-1PbnI3n+1 with A = methylammonium (MA) or formamidinium (FA) and n = 2, 3. Single-crystal structure analysis reveals the C2v symmetry of these crystal structures and substantial structural distortions, which enable Rashba and Dresselhaus band splitting and persistent spin texture, confirmed by DFT calculations. Measurements of the resulting symmetry-dependent properties, such as second harmonic generation, switchable photovoltaic effect, ferroelectric polarization, and low temperature photoluminescence show switchable ferroelectric semiconducting properties. These results introduce a general chemical design strategy toward polar symmetry by exploiting the complex interplay between asymmetric spacer cations and A-site cations in quasi-2D (n > 1) halide perovskites to realize new classes of multifunctional materials for future spin-orbitronic applications.
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