单独一对
化学
锑
二次谐波产生
结晶学
四面体
非线性光学
热液循环
八面体
带隙
相(物质)
晶体结构
谱线
无机化学
非线性系统
分子
光电子学
光学
物理
地质学
地震学
有机化学
量子力学
激光器
天文
作者
Qi Wei,Kui Wang,Chao He,Li Wei,Xiaofei Li,Shuo Zhang,Xing‐Tao An,Jinhua Li,Guo‐Ming Wang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-07-21
卷期号:60 (15): 11648-11654
被引量:45
标识
DOI:10.1021/acs.inorgchem.1c01653
摘要
Introducing stereochemically active lone-pair Sb3+ cations into sulfates, two three-dimensional (3D) antimony-sulfates, Sb4O5SO4 (1) and Sb4O(SO4)(OH)2 (2), were achieved under moderate hydrothermal conditions. Both structures are constructed by tetranuclear-{Sb4}-clusters-based layers and SO4 tetrahedra. However, owing to the different packing patterns of the layers, they display different characteristics: 1 exhibits a centrosymmetric structure while 2 possesses a noncentrosymmetric structure. UV–vis spectra show that they possess wide band gaps. Sb4O(SO4)(OH)2 is nonlinear optical (NLO) active with a second-harmonic generation (SHG) response of ∼1.2 times of KH2PO4, together with the phase-matchable capacity, endowing it a promising UV NLO material. The first-principle calculations were performed to elucidate the structure–property relationships. The results indicate that the lone pair stereoactivity of Sb3+ provides the large contribution to the macroscopic SHG effect.
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