Li Zhenhua, Liang Zhengli, Wan Jiahao, Liu Lehui, Wu Chunxiang, Wang Ping, Jiang Xingxing, Lin Zheshuai, Liu Hongming
Guangxi Key Laboratory of Electrochemical Energy Materials, School of Chemistry and Chemical Engineering, Guangxi University Nanning Guangxi 530004 China
Technical Institute of Physics and Chemistry, Chinese Academy of Science Beijing 100190 China
Chem Sci. 2025 Jan 15;16(7):3329-3335. doi: 10.1039/d4sc06620k. eCollection 2025 Feb 12.
Acentric crystalline materials are the cornerstone of numerous cutting-edge technologies and have been highly sought-after, but they are difficult to construct controllably. Herein, by introducing a new p-block element to break the symmetrical environment of the d transition metal in the centric matrix TiTeO, a novel acentric tellurite sulfate, namely Ti(TeO)(SO), was successfully constructed. In its structure, two types of p-block element-centered oxo-anionic groups, [TeO] and [SO], endow [TiO] with an out-of-center distortion along the local C[111] direction, which is rare in titanium oxides containing a lone-pair cation. The synergy of the distorted [TiO] octahedron, lone-pair [TeO] pyramid and rigid [SO] tetrahedron within its structure induces a strong second harmonic generation (SHG) response of 11.6 × KDP (KHPO), the largest value among mercury-free sulfates. Additionally, Ti(TeO)(SO) also shows the largest birefringence (0.145) among sulfates possessing an SHG response that is more than ten times that of KDP, showing huge potential as a nonlinear optical material. The successful implementation of the strategy of inducing intra-octahedral distortion in a d transition metal by different p-block elements provides new opportunities for constructing acentric structures and exploiting outstanding nonlinear optically active sulfates.
无对称中心的晶体材料是众多前沿技术的基石,备受追捧,但难以可控构建。在此,通过引入一种新的p区元素来打破中心基质TiTeO中d过渡金属的对称环境,成功构建了一种新型无对称中心的碲酸盐硫酸盐,即Ti(TeO)(SO)。在其结构中,两种以p区元素为中心的含氧阴离子基团[TeO]和[SO],使[TiO]沿局部C[111]方向发生偏离中心的畸变,这在含有孤对阳离子的钛氧化物中很少见。其结构中畸变的[TiO]八面体、孤对[TeO]金字塔和刚性[SO]四面体的协同作用,诱导出11.6×KDP(KHPO)的强二次谐波产生(SHG)响应,这是无汞硫酸盐中的最大值。此外,Ti(TeO)(SO)在具有SHG响应的硫酸盐中也表现出最大的双折射(0.145),是KDP的十多倍,作为非线性光学材料显示出巨大潜力。通过不同p区元素诱导d过渡金属八面体内畸变的策略的成功实施,为构建无对称中心结构和开发优异的非线性光学活性硫酸盐提供了新机遇。