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分级玫瑰状二硫化钼/金纳米复合材料上的共振辅助表面增强拉曼光谱放大

Resonance-Assisted Surface-Enhanced Raman Spectroscopy Amplification on Hierarchical Rose-Shaped MoS/Au Nanocomposites.

作者信息

Yu Hongyan, Sun Huanhuan, Ma Junjie, Han Boyang, Wang Rensheng, Ma Yun, Lou Gang, Song Yanping

机构信息

Key Laboratory of Solid State Optoelectronic Devices of Zhejiang Province, College of Physics and Electronic Information Engineering, Zhejiang Normal University, Jinhua 321004, China.

出版信息

Langmuir. 2024 Jan 9;40(1):380-388. doi: 10.1021/acs.langmuir.3c02635. Epub 2023 Dec 28.

Abstract

Surface-enhanced Raman spectroscopy (SERS) has emerged as a highly sensitive trace detection technique in recent decades, yet its exceptional performance remains elusive in semiconductor materials due to the intricate and ambiguous nature of the SERS mechanism. Herein, we have synthesized MoS nanoflowers (NFs) decorated with Au nanoparticles (NPs) by hydrothermal and redox methods to explore the size-dependence SERS effect. This strategy enhances the interactions between the substrate and molecules, resulting in exceptional uniformity and reproducibility. Compared to the unadorned Au nanoparticles (NPs), the decoration of Au NPs induces an n-type effect on MoS, resulting in a significant enhancement of the SERS effect. This augmentation empowers MoS to achieve a low limit of detection concentration of 2.1 × 10 M for crystal violet (CV) molecules and the enhancement factor (EF) is about 8.52 × 10. The time-stability for a duration of 20 days was carried out, revealing that the Raman intensity of CV on the MoS/Au-6 substrate only exhibited a reduction of 24.36% after undergoing aging for 20 days. The proposed mechanism for SERS primarily stems from the synergistic interplay among the resonance of CV molecules, local surface plasma resonance (LSPR) of Au NPs, and the dual-step charge transfer enhancement. This research offers comprehensive insights into SERS enhancement and provides guidance for the molecular design of highly sensitive SERS systems.

摘要

近几十年来,表面增强拉曼光谱(SERS)已成为一种高灵敏度的痕量检测技术,然而,由于SERS机制复杂且不明确,其卓越性能在半导体材料中仍难以实现。在此,我们通过水热法和氧化还原法合成了用金纳米颗粒(NPs)修饰的二硫化钼纳米花(NFs),以探索尺寸依赖性SERS效应。该策略增强了基底与分子之间的相互作用,从而实现了卓越的均匀性和可重复性。与未修饰的金纳米颗粒(NPs)相比,金纳米颗粒的修饰在二硫化钼上诱导了n型效应,导致SERS效应显著增强。这种增强使二硫化钼对结晶紫(CV)分子的检测浓度下限低至2.1×10⁻⁸ M,增强因子(EF)约为8.52×10⁴。进行了为期20天的时间稳定性测试,结果表明,在MoS₂/Au-6基底上的CV拉曼强度在老化20天后仅降低了24.36%。所提出的SERS机制主要源于CV分子的共振、金纳米颗粒的局域表面等离子体共振(LSPR)和双步电荷转移增强之间的协同相互作用。本研究为SERS增强提供了全面的见解,并为高灵敏度SERS系统的分子设计提供了指导。

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