化学
非线性光学
红外线的
多面体
各向异性
双折射
非线性光学
工作(物理)
非线性系统
配位复合体
红外光谱学
二次谐波产生
光学各向异性
结晶学
八面体
分子
四面体
光电子学
分子物理学
二硫键
纳米技术
化学物理
作者
Yumiao Niu,Yan Chun Xiao,Yidan Chen,Chu Chu,Daqing Yang,Ying Wang,Bingbing Zhang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2025-12-31
卷期号:65 (2): 1688-1697
被引量:4
标识
DOI:10.1021/acs.inorgchem.5c05438
摘要
The disulfide dianion [S 2 ] 2–, as an important structural motif in sulfides, can incorporate isolated S 2– to form homoatomic heteroleptic polyhedra [MS x (S 2 ) y ]. However, the sulfides that contain [MS x (S 2 ) y ] units have been rarely reported and have not been systematically investigated as infrared (IR) nonlinear optical (NLO) materials. It is verified in this work that the homoatomic heteroleptic coordination strategy enhances local structural asymmetry, leading to improved optical anisotropy and NLO performance. Three compounds, namely, ANb 2 PS 10 (A = K,Rb,Cs), were identified and prepared. They exhibit a large phase-matchable second-harmonic generation (SHG) response, with KNb 2 PS 10, RbNb 2 PS 10, and CsNb 2 PS 10 showing the effects of 1.5, 2.2, and 1.8 (×AgGaS 2 @2090 nm), respectively, and large birefringence (Δ n = 0.39@546 nm) with KNb 2 PS 10 as a representative. The first-principles calculations indicate that [Nb 2 S 4 (S 2 ) 4 ] 8– units play a dominant role in inducing strong SHG responses and large birefringence. By validating the homoatomic heteroleptic coordination strategy, this work opens avenues for the design of advanced optical materials.
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