SnS2纳米结构激发超灵敏SERS传感器PICT共振的形态学工程

IF 22.5
Yusi Peng, Weida Zhang, Meimei Xu, Shuai Zhao, Lili Yang, Dan Li, Masaki Tanemura, Zhengren Huang, Yong Yang
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引用次数: 0

摘要

近年来的研究表明,半导体的表面增强拉曼散射(SERS)灵敏度普遍低于贵金属衬底,开发超灵敏的半导体SERS衬底是一个紧迫的任务。本文通过密度泛函理论(DFT)从硫化物和硒化物中筛选出具有较好SERS性能的SnS2。在不添加任何表面活性剂或模板的情况下,通过调节反应物浓度来控制生长驱动力,制备出了堆叠纳米片(SNSs)、微球(MSs)和微花(MFs)的SnS2纳米结构,其超低检出限(lod)分别为10−12、10−13和10−11 M。据我们所知,这三种SnS2纳米结构的SERS灵敏度优于大多数报道的纯半导体,甚至可以与具有“热点”效应的贵金属平行。SnS2纳米结构的SERS增强是由于不同波长激发激光的光诱导电荷转移(PICT)共振的主要贡献。得益于SnS2纳米结构优异的SERS增强均匀性、通用性、稳定性、超高灵敏度,以及对不同探针分子激发的PICT共振增强不受其形态限制的优点,有望为半导体SERS技术的实际应用提供一类潜在的商用SERS活性材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Morphology Engineering of SnS2 Nanostructures to Stimulate PICT Resonance for Ultra-Sensitive SERS Sensors

Morphology Engineering of SnS2 Nanostructures to Stimulate PICT Resonance for Ultra-Sensitive SERS Sensors

Recent advances indicate the surface-enhanced Raman scattering (SERS) sensitivity of semiconductors is generally lower than that of noble metal substrates, and developing ultra-sensitive semiconductor SERS substrates is an urgent task. Here, SnS2 with better SERS performance is screened out from sulfides and selenides by density functional theory (DFT) calculations. Through adjusting the concentration of reactants to control the growth driving force without any surfactants or templates, SnS2 nanostrctures of stacked nanosheets (SNSs), microspheres (MSs) and microflowers (MFs) are developed, which all exhibit ultra-low limit of detections (LODs) of 10−12, 10−13, and 10−11 M, respectively. To the best of our knowledge, the SERS sensitivity of these three kinds of SnS2 nanostrctures are superior to most of the reported pure semiconductors and even can be parallel to the noble metals with a “hot spot” effect. This extraordinary SERS enhancement of SnS2 nanostrctures is originated from the dominated contribution of photo-induced charge transfer (PICT) resonance with different wavelength excitation lasers. Benefitting to the excellent SERS enhanced uniformity, generality, stability, ultra-high sensitivity of SnS2 nanostrctures, and the advantages that the PICT resonance enhancement excited for different probe molecules is not limited by its morphology, it is expected to provide a class of potential commercial SERS-active materials for the practical application of semiconductor-based SERS technology.

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