Polar-Layer-Driven Reconstruction of a Noncentrosymmetric Vandate Mid-Infrared Nonlinear-Optical Crystal.

Inorg Chem

Beijing Center for Crystal Research and Development, Key Laboratory of Functional Crystals and Laser Technology, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

Published: November 2024

AI Article Synopsis

Article Abstract

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 KZnVO as a prototype compound, a novel vandate KZnVOBr (KZVB) was rationally synthesized via a multiple sites-oriented cosubstition method. KZVB containing two types of NLO-active units of V d and Zn d cations can be utilized as a mid-infrared NLO crystal with a remarkable NLO response comparable to that of nonoxide AgGaS. This work not only broadens the effective strategy for designing novel NCS compounds but also provides a progressive development of NLO materials.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.inorgchem.4c04300DOI Listing

Publication Analysis

Top Keywords

nlo crystal
8
nlo-active units
8
nlo
5
polar-layer-driven reconstruction
4
reconstruction noncentrosymmetric
4
noncentrosymmetric vandate
4
vandate mid-infrared
4
mid-infrared nonlinear-optical
4
crystal
4
nonlinear-optical crystal
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!