Zhang Haijun, Jiang Xingxing, Zhang Yiran, Duanmu Kaining, Wu Chao, Lin Zheshuai, Xu Jun, Yang Jinhu, Huang Zhipeng, Humphrey Mark G, Zhang Chi
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.
J Am Chem Soc. 2024 Oct 7. doi: 10.1021/jacs.4c09172.
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.
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。