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通过合理的交叉取代策略在铕基硫族化合物中实现优异的红外非线性光学性能

Realizing Excellent Infrared Nonlinear Optical Performance in Eu-Based Chalcogenides via Rational Cross Substitution Strategy.

作者信息

Feng Ping, Zhou Sheng-Hua, Li Bing-Xuan, Zhang Jia-Xiang, Ran Mao-Yin, Wu Xin-Tao, Lin Hua, Zhu Qi-Long

机构信息

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 350108, China.

出版信息

ACS Appl Mater Interfaces. 2024 Oct 2;16(39):52682-52691. doi: 10.1021/acsami.4c11949. Epub 2024 Sep 22.

Abstract

In recent years, rare-earth-based chalcogenides have gained attention promising materials in the field of infrared nonlinear optical (IR-NLO) applications owing to their exceptional physicochemical properties. However, they frequently encounter challenges such as adverse two-photon absorption and low laser-induced damage thresholds (LIDTs) caused by narrow optical band gaps (), which limit their practical utility. In this study, we started with the centrosymmetric (CS) parent compound EuGaS to develop two new noncentrosymmetric (NCS) Eu-based chalcogenides, namely, EuZnSiS and EuCdSiS, employing a rational cross-substitution strategy. Despite having identical stoichiometry, both compounds crystallize in distinct NCS orthorhombic space groups [2 (no. 43) 2 (no. 40)], as confirmed by single-crystal structure analysis. Their crystal structures feature highly distorted tetrahedral motifs interconnected via corner-sharing, forming unique two-dimensional layers that host Eu cations. Furthermore, both compounds exhibit robust phase-matching second-harmonic generation (SHG) intensities of 1.5 × AgGaS for EuZnSiS and 2.8 × AgGaS for EuCdSiS under 2050 nm excitation. They also demonstrate high LIDTs (approximately 14-17 × AgGaS), wide (>2.5 eV), and transparency windows extending up to 18.2 μm. Particularly noteworthy, EuCdSiS stands out as a pioneering example in the Eu-based IR-NLO system for successfully combining a broad E (>2.56 eV, equivalent to that of AgGaS) with a significant SHG effect (>1.0 × AgGaS) simultaneously. Structural analyses and theoretical insights underscore that the reasonable combination of asymmetric functional units plays a pivotal role in driving the CS-to-NCS structural transformation and enhancing the NLO and linear optical properties of these Eu-based chalcogenides. This study presents a promising chemical pathway for advancing rare-earth-based functional materials and suggests exciting opportunities for their future applications in IR-NLO technologies.

摘要

近年来,基于稀土的硫族化物因其优异的物理化学性质,在红外非线性光学(IR-NLO)应用领域成为备受关注的有前景材料。然而,它们经常遇到诸如不利的双光子吸收和由窄光学带隙导致的低激光诱导损伤阈值(LIDTs)等挑战,这限制了它们的实际应用。在本研究中,我们以中心对称(CS)母体化合物EuGaS为起始,采用合理的交叉取代策略开发了两种新的非中心对称(NCS)Eu基硫族化物,即EuZnSiS和EuCdSiS。尽管具有相同的化学计量比,但通过单晶结构分析证实,这两种化合物都结晶于不同的NCS正交空间群[2(编号43)2(编号40)]。它们的晶体结构具有通过角共享相互连接的高度扭曲的四面体 motif,形成容纳Eu阳离子的独特二维层。此外,在2050 nm激发下,这两种化合物都表现出稳健的相位匹配二次谐波产生(SHG)强度,EuZnSiS为1.5×AgGaS,EuCdSiS为2.8×AgGaS。它们还展示出高LIDTs(约为14 - 17×AgGaS)、宽的(>2.5 eV)以及延伸至18.2μm的透明窗口。特别值得注意的是,EuCdSiS在Eu基IR-NLO体系中脱颖而出,成为成功将宽的E(>2.56 eV,等同于AgGaS)与显著的SHG效应(>1.0×AgGaS)同时结合的开创性例子。结构分析和理论见解强调,不对称功能单元的合理组合在驱动CS到NCS的结构转变以及增强这些Eu基硫族化物的NLO和线性光学性质方面起着关键作用。本研究为推进基于稀土的功能材料提供了一条有前景的化学途径,并为它们未来在IR-NLO技术中的应用暗示了令人兴奋的机会。

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