Wei Qi, Zhang Qingyun, Xiang Longjun, Zhang Shihao, Liu Jianpeng, Yang Xiaoyu, Ke Youqi, Ning Zhijun
School of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
J Phys Chem Lett. 2021 Jul 22;12(28):6492-6498. doi: 10.1021/acs.jpclett.1c01675. Epub 2021 Jul 9.
Chiral hybrid organic-inorganic perovskites (chiral HOIPs) present potential spintronic and spin-optoelectronic applications due to their unique spin-related properties. However, the spin physics in chiral HOIPs has rarely been explored by theoretical studies. Here, with first-principles calculations, we investigate the spin characteristics of the Pb-I based chiral HOIPs and propose an effective approach to significantly increase the spin splitting with a halogen-substituted chiral molecule. Compared to the value of 13 meV without halogen substitution, the spin splitting energy can be significantly enhanced to 73, 90, and 105 meV with F, Cl, and Br substitution, respectively. A · model Hamiltonian based on a symmetry argument reveals that the halogen substitution enhances the local electric field, inducing distortion of the PbI octahedron. Further calculation demonstrates that halogen substitution can strongly modify the electrostatic potential surface of the chiral molecules. This work presents an effective molecular engineering approach to modulate spin splitting of chiral HOIPs, shedding light on the design of spintronic materials.
手性有机-无机杂化钙钛矿(手性HOIPs)因其独特的自旋相关特性而展现出潜在的自旋电子学和自旋光电子学应用前景。然而,理论研究很少探索手性HOIPs中的自旋物理。在此,通过第一性原理计算,我们研究了基于Pb-I的手性HOIPs的自旋特性,并提出了一种有效的方法,通过卤代手性分子显著增加自旋分裂。与未进行卤素取代时13 meV的值相比,分别用F、Cl和Br取代时,自旋分裂能量可显著提高到73 meV、90 meV和105 meV。基于对称性论证的模型哈密顿量表明,卤素取代增强了局部电场,导致PbI八面体发生畸变。进一步的计算表明,卤素取代能强烈改变手性分子的静电势面。这项工作提出了一种有效的分子工程方法来调节手性HOIPs的自旋分裂,为自旋电子材料的设计提供了思路。