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通过结合孤对电子和π共轭基团设计具有大双折射的混合锑基非线性光学晶体

Designing Hybrid Sb-Based Nonlinear Optical Crystals with Large Birefringence by Combining the Lone Pair and π-Conjugated Genes.

作者信息

Yang Kang, Wang Duanliang, Liu Fangcong, Zhu Chuanrui, Wang Qiyao, Wu Kui, Wang Jiyang, Shen Chuanying

机构信息

College of Physics and Engineering, Qufu Normal University, Qufu 273165, China.

State Key Laboratory of Crystal Materials, Institute of Crystal Materials, Shandong University, Jinan, Shandong 250100, China.

出版信息

Inorg Chem. 2025 Aug 11;64(31):16258-16266. doi: 10.1021/acs.inorgchem.5c02960. Epub 2025 Jul 28.

Abstract

The combination of two types of NLO-active units into one compound is beneficial to produce outstanding second harmonic generation (SHG) crystals. Herein, by incorporation of Sb with SCALP electrons into planar π-conjugated 2-(aminomethyl)pyridine, two new noncentrosymmetric hybrid antimony (Sb)-based halides with zero-dimension (0D) structure, (CHN)SbX·X·HO (X = Cl and Br), have been synthesized. As expected, both compounds exhibit obviously SHG responses of 0.56 and 0.83 × KDP. Moreover, they also show clearly ultraviolet (UV) transparency with the ultraviolet cutoff edges at 360 and 393 nm, indicating their potential application as SHG crystals. Structural and theoretical analysis imply that their prominently optical properties are largely ascribed to the collaborative contribution of organic π-conjugated cations and the distorted Sb-halogenated polyhedrons. Additionally, a large birefringence of 0.156 and 0.147@1064 nm, which can be ascribed to the strong aeolotropic conjugated π electron distribution of their organic groups, were determined for (CHN)SbCl·Cl·HO and (CHN)SbBr·Br·HO, respectively. Intriguingly, (CHN)SbCl·Cl·HO also presents obvious photoluminescence, which mainly derives from the radiation recombination of triplet self-trapped excitons. This work proves that the combination of SCALP elements with organic π-conjugated cations is an effective strategy to explore novel NLO materials with high optical performances.

摘要

将两种类型的非线性光学活性单元结合在一种化合物中有利于制备出优异的二次谐波产生(SHG)晶体。在此,通过将具有孤对电子的锑与平面π共轭的2-(氨甲基)吡啶相结合,合成了两种具有零维(0D)结构的新型非中心对称杂化锑基卤化物(CH₃NH₃)SbX₃·X·H₂O(X = Cl和Br)。正如预期的那样,这两种化合物均表现出明显的SHG响应,分别为0.56和0.83×KDP。此外,它们还在360和393 nm处具有明显的紫外(UV)截止边缘,显示出作为SHG晶体的潜在应用价值。结构和理论分析表明,它们突出的光学性质很大程度上归因于有机π共轭阳离子和扭曲的Sb-卤化物多面体的协同作用。此外,对于(CH₃NH₃)SbCl₃·Cl·H₂O和(CH₃NH₃)SbBr₃·Br·H₂O,分别测定了在1064 nm处0.156和0.147的大双折射,这可归因于其有机基团强烈的各向异性共轭π电子分布。有趣的是,(CH₃NH₃)SbCl₃·Cl·H₂O还呈现出明显的光致发光,这主要源于三重态自陷激子的辐射复合。这项工作证明,将具有孤对电子的元素与有机π共轭阳离子相结合是探索具有高光性能的新型非线性光学材料的有效策略。

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