化学
多面体
紫外线
铅(地质)
非线性光学
Crystal(编程语言)
晶体结构
非线性系统
化学工程
纳米技术
组合化学
光化学
光电子学
结晶学
组合数学
物理
材料科学
数学
地貌学
量子力学
计算机科学
工程类
程序设计语言
地质学
作者
Shuangying Lei,Xiangyu Zhang,Wen-Xiu Bao,Ruibiao Fu,Shuangcheng Li,Jun Zeng,Yiting Luo,Zuju Ma
标识
DOI:10.1021/acs.inorgchem.5c01343
摘要
The exploration of ultraviolet (UV) nonlinear optical (NLO) crystals owning a strong second-harmonic generation (SHG) response has consistently been a difficult task. Herein, we have controllably tailored the lead-oxychloride polyhedron by tuning the amount of KCl under mixed-solvothermal conditions to afford a new strong UV NLO crystal, K3[Pb2Cl5(HCOO)2]·H2O. Interestingly, benefiting from the oriented arrangement of the large [Pb6Cl24O12] rings, the microscopic second-order susceptibilities of the distorted [PbCl5O2] polyhedrons are effectively superimposed. Remarkably, K3[Pb2Cl5(HCOO)2]·H2O owns a unique 3D polar framework, a strong phase-matchable SHG response that is 3.1 times as strong as KDP, a suitable birefringence of 0.108@1064 nm, a broad high transparent window extending to 340 nm in the UV region, and feasible crystal growth. Dipole moment and theoretical calculations elucidate that the strong SHG response originates from the distorted [PbCl5O2] polyhedron. This study will shed light on the development of subsequent UV NLO crystals.
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