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通过硫氰酸锌的维度工程实现强紫外-可见-近红外二次谐波产生

Toward Strong UV-Vis-NIR Second-Harmonic Generation by Dimensionality Engineering of Zinc Thiocyanates.

作者信息

Zhang Haijun, Jiang Xingxing, Zhang Yiran, Duanmu Kaining, Wu Chao, Lin Zheshuai, Xu Jun, Yang Jinhu, Huang Zhipeng, Humphrey Mark G, Zhang Chi

机构信息

China-Australia Joint Research Center for Functional Molecular Materials, School of Materials Science and Engineering, Ocean University of China, Qingdao 266404,, China.

School of Chemical Science and Engineering & Tongji Hospital, School of Medicine, Tongji University, Shanghai 200092, China.

出版信息

J Am Chem Soc. 2024 Oct 7. doi: 10.1021/jacs.4c09172.

Abstract

The precise modulation of the spatial orientations and connection modes of primitives is vital for certain critically important optical functions for nonlinear optical (NLO) materials (specifically, second-harmonic generation (SHG) and optical bandgap); however, we are yet to achieve a sufficient level of control for the designed construction of efficient broadband NLO materials. Exploiting the changes in microscopic polarization that may result from dimensional increase, we propose herein a zero-dimensional (0D)-to-three-dimensional (3D) dimensionality-increase strategy to realize strong broadband SHG responses for the first time. The novel 3D pseudo diamond-like Zn(SCN) has been synthesized by removing SHG-inactive [NH] counter cations and HO molecules that are located between the adjacent discrete [Zn(SCN)] building blocks within the 0D (NH)Zn(SCN)·3HO. The 0D-to-3D dimensionality engineering, proceeding from (NH)Zn(SCN)·3HO to Zn(SCN), results in significantly enhanced SHG responses and efficient broadband activity (8 × KHPO @ 1064 nm, 4.18 eV bandgap for the former c.f. 2 × β-BaBO @ 380 nm, 30 × KHPO @ 1064 nm, 2 × KTiOPO @ 2100 nm, 4.78 eV bandgap for the latter) from the UV to the NIR regions (SHG@300-1050 nm). Theoretical calculations and crystal structure analyses reveal that the coordination-bond-connected [Zn(SCN)] building blocks within the diamond-like structure of Zn(SCN) are responsible for its giant broadband SHG responses.

摘要

对于非线性光学(NLO)材料的某些至关重要的光学功能(具体而言,二次谐波产生(SHG)和光学带隙),原语基元的空间取向和连接模式的精确调制至关重要;然而,我们尚未实现对高效宽带NLO材料的设计构建进行足够程度的控制。利用维度增加可能导致的微观极化变化,我们在此提出一种从零维(0D)到三维(3D)的维度增加策略,以首次实现强烈的宽带SHG响应。通过去除0D(NH₄)Zn(SCN)·3H₂O中相邻离散[Zn(SCN)]结构单元之间的SHG无活性[NH₄]⁺抗衡阳离子和H₂O分子,合成了新型的3D类金刚石Zn(SCN)。从(NH₄)Zn(SCN)·3H₂O到Zn(SCN)的0D到3D维度工程,导致SHG响应显著增强,并在从紫外到近红外区域(300 - 1050 nm的SHG)实现了高效的宽带活性(前者在1064 nm处为8×KDP,带隙为4.18 eV,相比之下,后者在380 nm处为2×β - BaB₂O₄,在1064 nm处为30×KDP,在2100 nm处为2×KTiOPO₄,带隙为4.78 eV)。理论计算和晶体结构分析表明,Zn(SCN)类金刚石结构内通过配位键连接的[Zn(SCN)]结构单元是其巨大宽带SHG响应的原因。

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