Leng Xudong, Hu Mei, Jing Qun, Duan Haiming, Chen Henglei, Cui Xiuhua
Xinjiang Key Laboratory of Solid State Physics and Devices, School of Physical Science and Technology, Xinjiang University, Urumqi 830017, China.
Nanomaterials (Basel). 2024 Apr 1;14(7):617. doi: 10.3390/nano14070617.
Introducing post-transition metal cations is an excellent strategy for enhancing optical properties. This paper focuses on four isomers, namely the XPOI (X = Pb, Sn, Ba, and Sr) series. For the first time, the paper's attention is paid to the changes in electronic structure, as well as refractive indices and birefringence, with and without the inclusion of spin-orbit effects in this series. The first-principles results show that spin-orbit effects of the 5p and 6p states found in these compounds lead to splitting of the bands, narrowing of the band gap, enhancement of the lone-pair stereochemistry, and enhancement of the refractive indices and birefringence. Moreover, a comparison of the lone-pair electron phosphates, XPOI (X = Pb and Sn), and the isomeric alkaline earth metal phosphates, XPOI (X = Ba and Sr), reveals that changes in the band structure have a greater effect on the enhancement of the birefringence than the slight enhancement of the lone-pair stereochemical activity. This study has important implications for a deeper understanding of the optical properties of crystals and the design of novel optical materials.
引入后过渡金属阳离子是增强光学性质的一种出色策略。本文聚焦于四种异构体,即XPOI(X = Pb、Sn、Ba和Sr)系列。本文首次关注了该系列中包含和不包含自旋轨道效应时电子结构、折射率和双折射的变化。第一性原理结果表明,这些化合物中5p和6p态的自旋轨道效应导致能带分裂、带隙变窄、孤对立体化学增强以及折射率和双折射增强。此外,对孤对电子磷酸盐XPOI(X = Pb和Sn)与异构碱土金属磷酸盐XPOI(X = Ba和Sr)的比较表明,能带结构的变化对双折射增强的影响比对孤对立体化学活性的轻微增强更大。这项研究对于更深入理解晶体的光学性质和新型光学材料的设计具有重要意义。