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探究取向无序立方相杂化钙钛矿的电子结构

Probing the Electronic Structure of Hybrid Perovskites in the Orientationally Disordered Cubic Phase.

作者信息

Nandi Pronoy, Pandey S K, Giri Chandan, Singh Vijay, Petaccia L, Manju U, Mahanti Subhendra D, Topwal D

机构信息

Institute of Physics, Sachivalaya Marg, Bhubaneswar 751005, Odisha, India.

Homi Bhabha National Institute, Training School Complex, Anushakti Nagar, Mumbai 400085, India.

出版信息

J Phys Chem Lett. 2020 Jul 16;11(14):5719-5727. doi: 10.1021/acs.jpclett.0c01386. Epub 2020 Jul 6.

Abstract

Hybrid organic-inorganic lead halide perovskites are projected as new generation photovoltaic and optoelectronic materials with improved efficiencies. However, their electronic structure so far remains poorly understood, particularly in the orientationally disordered cubic phase. We performed electronic structure investigations using angle-resolved photoemission spectroscopy on two prototypical samples (MAPbBr and MAPbCl) in their cubic phase, and the results are compared with the calculations within two theoretical models where MA is orientationally (1) disordered (MA ion is replaced by spherically symmetric Cs ion) and (2) ordered (MA oriented along (100) direction) but keeping the symmetry of the unit cell cubic. Degeneracy of the valence bands and behavior of constant energy contours are consistent with model 1, which supports strongly the disordered nature of the orientation of the MA ions in the cubic phase. Band structure calculations also reveal that spin-orbit coupling induced Rashba splitting is suppressed by the orientational disorder.

摘要

有机-无机杂化卤化铅钙钛矿被视为具有更高效率的新一代光伏和光电子材料。然而,到目前为止,它们的电子结构仍知之甚少,尤其是在取向无序的立方相中。我们使用角分辨光电子能谱对两个立方相的典型样品(MAPbBr和MAPbCl)进行了电子结构研究,并将结果与两个理论模型的计算结果进行了比较,其中MA在取向方面:(1)无序(MA离子被球对称的Cs离子取代)和(2)有序(MA沿(100)方向取向),但保持晶胞立方对称。价带简并和等能轮廓行为与模型1一致,这有力地支持了立方相中MA离子取向的无序性质。能带结构计算还表明,自旋-轨道耦合诱导的Rashba分裂被取向无序抑制。

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