化学
红外线的
极地的
非线性光学
图层(电子)
Crystal(编程语言)
红外光谱学
非线性系统
结晶学
光学
有机化学
天文
物理
量子力学
计算机科学
程序设计语言
作者
Haochen Li,Haotian Tian,Pifu Gong,Tianyu Wang,Qian Wu,Mingjun Xia
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-10-28
卷期号:63 (45): 21753-21757
被引量:9
标识
DOI:10.1021/acs.inorgchem.4c04300
摘要
Noncentrosymmetry (NCS) is essential for a second-harmonic nonlinear-optical (NLO) crystal; however, the tailored synthesis of NCS materials has historically posed significant challenges because the adjacent dipole moments of constituted NLO-active units in the structure tend to align in opposite directions, resulting in the NLO effect being canceled as in a centrosymmetric (CS) crystal. In this work, we propose a polar-layer-driven strategy, wherein a polarization-layered framework is constructed to constrain the dipole moment to align in the same direction, thereby facilitating the formation of the NCS structure. Taking the layered structure CS K2ZnV2O7 as a prototype compound, a novel vandate K4ZnV5O15Br (KZVB) was rationally synthesized via a multiple sites-oriented cosubstition method. KZVB containing two types of NLO-active units of V5+ d0 and Zn2+ d10 cations can be utilized as a mid-infrared NLO crystal with a remarkable NLO response comparable to that of nonoxide AgGaS2. This work not only broadens the effective strategy for designing novel NCS compounds but also provides a progressive development of NLO materials.
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