Coulomb attraction driven spontaneous molecule-hotspot pairing enables universal, fast, and large-scale uniform single-molecule Raman spectroscopy

Raman spectroscopy offers a great power to detect, analyze and identify molecules, and monitor their temporal dynamics and evolution when combined with single-molecule surface-enhanced Raman scattering (SM-SERS) substrates. Here we present a SM-SERS scheme that involves simultaneously giant chemical enhancement from WS2 2D materials, giant electromagnetic enhancement from plasmonic nanogap hot spot, and inhibition of molecular fluorescence influence under near-infrared laser illumination. Remarkably we find Coulomb attraction between analyte and gold nanoparticle can trigger spontaneous formation of molecule-hotspot pairing with high precision, stability and robustness. The scheme has enabled realization of universal, robust, fast, and large-scale uniform SM-SERS detection for three Raman molecules of rhodamine B, rhodamine 6G, and crystal violet with a very low detection limit of 10−16 M and at a very fast spectrum acquisition time of 50 ms.

Authors

Publication Details

Journal
Opto-Electronic Advances
Published
2025-01-01
DOI
https://doi.org/10.29026/oea.2025.240309
Citations
1
Primary Topic
Spectroscopy Techniques in Biomedical and Chemical Research
Type
article
Field-Weighted Citation Impact
1.63
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article

Coulomb attraction driven spontaneous molecule-hotspot pairing enables universal, fast, and large-scale uniform single-molecule Raman spectroscopy

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Opto-Electronic Advances
Spectroscopy Techniques in Biomedical and Chemical Research
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article

Coulomb attraction driven spontaneous molecule-hotspot pairing enables universal, fast, and large-scale uniform single-molecule Raman spectroscopy

Zihan Gao, Haiyao Yang, Lihong Hong, Zhi‐Yuan Li, Jianzhi Zhang
article en
1 citations

Abstract

Raman spectroscopy offers a great power to detect, analyze and identify molecules, and monitor their temporal dynamics and evolution when combined with single-molecule surface-enhanced Raman scattering (SM-SERS) substrates. Here we present a SM-SERS scheme that involves simultaneously giant chemical enhancement from WS2 2D materials, giant electromagnetic enhancement from plasmonic nanogap hot spot, and inhibition of molecular fluorescence influence under near-infrared laser illumination. Remarkably we find Coulomb attraction between analyte and gold nanoparticle can trigger spontaneous formation of molecule-hotspot pairing with high precision, stability and robustness. The scheme has enabled realization of universal, robust, fast, and large-scale uniform SM-SERS detection for three Raman molecules of rhodamine B, rhodamine 6G, and crystal violet with a very low detection limit of 10−16 M and at a very fast spectrum acquisition time of 50 ms.

Opto-Electronic AdvancesVol. 8(7)
Openalex Percentile: Top 13%
Spectroscopy Techniques in Biomedical and Chemical Research
1.63
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