Resonance-Assisted Surface-Enhanced Raman Spectroscopy Amplification on Hierarchical Rose-Shaped MoS 2 /Au Nanocomposites

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 nanofl...

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Veröffentlicht in:Langmuir 2024-01, Vol.40 (1), p.380-388
Hauptverfasser: Yu, Hongyan, Sun, Huanhuan, Ma, Junjie, Han, Boyang, Wang, Rensheng, Ma, Yun, Lou, Gang, Song, Yanping
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container_issue 1
container_start_page 380
container_title Langmuir
container_volume 40
creator Yu, Hongyan
Sun, Huanhuan
Ma, Junjie
Han, Boyang
Wang, Rensheng
Ma, Yun
Lou, Gang
Song, Yanping
description 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.
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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. 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