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    Blinking in surface-enhanced Raman spectrum beyond a single molecule

    Siyang Ye1, Kuanyu Ma1, Qihang Zhang1, Jiamin Lin2, Hanyu Liu1, Shengnan Feng3, Daocheng Hong1,4, Zhen Shen1, Sushu Wan1 et al.

    Xiaoyong Wang3, Weigao Xu2, and Yuxi Tian1,*

    • 1State Key Laboratory of Analytical Chemistry for Life Science, Key Laboratory of Mesoscopic Chemistry of MOE and School of Chemistry and Chemical Engineering, Nanjing University, 210023 Nanjing, China
    • 2State Key Laboratory of Coordination Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China
    • 3National Laboratory of Solid State Microstructures, School of Physics, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, China
    • 4Key Laboratory for Advanced Technology in Environmental Protection of Jiangsu Province, Yancheng Institute of Technology, Yancheng 224051, China

    • *Contact author: tyx@nju.edu.cn

    Phys. Rev. B 112, 075428 – Published 26 August, 2025

    DOI: https://doi.org/10.1103/4yg7-1f85

    Abstract

    Intermittent emission is a special characteristic of single molecule fluorescence, which is also called fluorescence blinking [Nature (London) 388, 355 (1997), Science 277, 1074 (1997)] and has also been observed in 0D [Nature (London) 383, 802 (1996)], 1D [Nat. Phys. 4, 519 (2008)] and 2D materials [Nature (London) 541, 62 (2017)]. The surface enhanced Raman spectrum (SERS) of a single molecule also shows blinking, which is commonly attributed to the movement of the molecule in and out of the active site of the metal nanoparticle [Science 275, 1102 (1997)]. For bulk samples, it is reasonable that no fluorescence or Raman blinking can be observed due to ensemble averaging from numerous molecules. In this work, however, we observed SERS blinking of bulk samples around a single gold nanorod (GNR) in solid matrices. Such SERS blinking behavior can be observed for different samples once the GNR is excited resonantly. These results suggest an intriguing mechanism of SERS blinking that does not require a single molecule. We propose two possible mechanisms that can explain the experimental results and suggest reconsidering the physical picture of the SERS blinking behaviors in both ensemble and single-molecule measurements.

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