卤化物
结晶学
材料科学
化学物理
凝聚态物理
化学
无机化学
物理
作者
Willa Mihalyi‐Koch,Songhao Guo,Zhenbang Dai,Dongxu Pan,David P. Lafayette,Jason M. Scheeler,Kyana M. Sanders,Simon J. Teat,John C. Wright,Xujie Lü,Andrew M. Rappe,Song Jin
出处
期刊:Chem
[Elsevier]
日期:2024-07-01
卷期号:10 (7): 2180-2195
被引量:4
标识
DOI:10.1016/j.chempr.2024.03.012
摘要
Hybrid 2D halide perovskites are tunable semiconductors that exhibit diverse structural symmetry and spin-orbit coupling effects. We examine a series of globally centrosymmetric n = 2 Ruddlesden-Popper (RP) lead iodide perovskites containing six different A-site cations, (PA)2(A)Pb2I7 [PA = pentylammonium]. Despite local structural distortions caused by oversized A-cations, all six structures are globally centrosymmetric, confirmed through second harmonic generation (SHG) measurements. However, in three of these 2D perovskites, the hydrogen bonding interaction between the A-cation and perovskite cage results in individual monolayers that lack inversion symmetry. Band structure calculations reveal Rashba band splitting due to this monolayer polarization, which is strongest in (PA)2(EA)Pb2I7 (EA = ethylammonium). Applying high pressure unmasks the non-centrosymmetry in bulk crystals with hidden non-centrosymmetry, leading to substantial SHG signal. A survey of reported crystal structures reveals that such hidden non-centrosymmetry is prevalent among 2D perovskites. These unexplored centrosymmetric 2D perovskites could be utilized for spin-orbitronic applications.
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