化学
钒酸盐
四面体
钒
二次谐波产生
晶体结构
带隙
氢键
Atom(片上系统)
空间组
结晶学
失真(音乐)
分子
无机化学
X射线晶体学
凝聚态物理
光学
光电子学
物理
衍射
嵌入式系统
有机化学
放大器
CMOS芯片
激光器
计算机科学
作者
Zhiyong Bai,Yunseung Kuk,Jihyun Lee,Heewon Kim,Kang Min Ok
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-02-05
卷期号:63 (7): 3578-3585
被引量:1
标识
DOI:10.1021/acs.inorgchem.3c04484
摘要
A new guanidinium-templated vanadate, [C(NH2)3]3VO4·2H2O, has been synthesized in a phase-pure form. It crystallizes in a noncentrosymmetric polar space group, Cc, and the crystal structure is built upon a framework of guanidinium, vanadate tetrahedra, and water molecules linked by hydrogen bonds. Notably, optical measurements reveal that the material exhibits an approximately 9.6-fold enhancement in second-harmonic generation efficiency compared to its phosphate analogue. The enhancement can be attributed to the increased geometrical distortion of the VO4 tetrahedra. Furthermore, we found that the coordination number of the central vanadium atom significantly affects the optical band gaps. Among various coordination numbers, the 4-coordinate VO4 tetrahedra are found to be more favorable for widening the optical band gap of materials compared to the 5- and 6-coordinate vanadium polyhedra, as demonstrated by this work.
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