Zhang Jia-Xiang, Zhou Sheng-Hua, Wu Xin-Tao, Lin Hua, Zhu Qi-Long
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350002, China.
Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China, Fuzhou, 350002, China.
Angew Chem Int Ed Engl. 2025 Jul;64(27):e202506658. doi: 10.1002/anie.202506658. Epub 2025 May 7.
The simultaneous optimization of large birefringence (Δn, a linear optical property) and strong second-harmonic generation (SHG, a nonlinear optical (NLO) property) in a single crystal remains a significant challenge due to the inherently distinct structural requirements for these properties. Although nonbonding electrons have been extensively studied in oxides and chalcogenides, research has predominantly focused on their role along polar axes, leaving their influence along axes in tetrahedral stacking largely unexplored. Herein, we propose a nonbonding electron-inversion strategy to overcome phase-matching limitations in defect diamond-like structures. By incorporating T2-[GaS] supertetrahedral motifs, we successfully synthesized [BaCl][CdGaS] (space group: I ), which exhibits a 219% enhancement in Δn compared to the nonphase-matching parent structure CdGaS. The weakly bound nonbonding electrons, governed by atomic potentials, demonstrate strong SHG responses under optical fields. The compound [BaCl][CdGaS] not only achieves a broad transmission range (0.28-18.6 µm) and a high laser-induced damage threshold (40.1 × AgGaS) but also optimally balances a wide bandgap (E = 3.58 eV) and a large SHG response (1.4 × AgGaS), representing one of the best-performing Cd-based materials to date. This work introduces the first phase-matching design strategy based on nonbonding electron-driven structure-property relationships, providing critical insights for the rational design of high-performance NLO materials.
由于大双折射(Δn,一种线性光学性质)和强二次谐波产生(SHG,一种非线性光学(NLO)性质)在单晶中的同时优化对结构的要求本质上截然不同,因此仍然是一项重大挑战。尽管非键电子在氧化物和硫族化物中已得到广泛研究,但研究主要集中在它们沿极性轴的作用,而它们在四面体堆积中沿 轴的影响在很大程度上尚未被探索。在此,我们提出一种非键电子反转策略来克服类金刚石缺陷结构中的相位匹配限制。通过引入T2-[GaS]超四面体 motif,我们成功合成了[BaCl][CdGaS](空间群:I ),与非相位匹配的母体结构CdGaS相比,其Δn提高了219%。受原子势支配的弱束缚非键电子在光场下表现出强烈的SHG响应。化合物[BaCl][CdGaS]不仅实现了宽透射范围(0.28 - 18.6 µm)和高激光诱导损伤阈值(40.1×AgGaS),还最佳地平衡了宽带隙(E = 3.58 eV)和大SHG响应(1.4×AgGaS),是迄今为止性能最佳的镉基材料之一。这项工作引入了基于非键电子驱动的结构 - 性质关系的首个相位匹配设计策略,为高性能NLO材料的合理设计提供了关键见解。