TY - GEN
T1 - Fabrication of SERS substrates via femtosecond laser reduction of silver nitrate solution
T2 - 5th International Conference on Laser, Optics, and Optoelectronic Technology, LOPET 2025
AU - Wang, Sumei
AU - Liu, Jiangfeng
N1 - Publisher Copyright:
© COPYRIGHT SPIE.
PY - 2025/8/20
Y1 - 2025/8/20
N2 - Surface-enhanced Raman scattering (SERS) technology has been extensively applied in various fields, particularly in trace detection. Nevertheless, the prevailing preparation methods currently suffer from several drawbacks, including intricate preparation procedures, elevated costs, and poor stability. In this work, we center on the fabrication process of SERS substrates via femtosecond laser photoreduction. By capitalizing on the characteristics of high instantaneous power and ultra-short pulse duration of femtosecond lasers, and taking advantage of the property of the weak Raman background spectrum of the polydimethylsiloxane (PDMS) film, a high-density nanostructure with remarkable enhancement performance is formed on the film. Silver nanostructures on PDMS are characterized with scanning electron microscope (SEM). Subsequently, the optimal process parameters are deduced through the analysis of the Raman spectra of samples processed under different conditions. Additionally, the hydrophobic properties, detection stability, and sensitivity of the substrate surface are evaluated. The Raman spectral results demonstrate that the developed SERS substrate exhibits an outstanding enhancement effect, with a detection limit of 10⁻⁸ M for Rhodamine 6G (R6G). Moreover, it possesses excellent stability, with a relative standard deviation of less than 10%. In comparison with conventional methods, this approach eliminates the utilization of toxic chemical reagents and circumvents complex and time-consuming process steps, thereby offering a novel strategy for the rapid fabrication of SERS substrates.
AB - Surface-enhanced Raman scattering (SERS) technology has been extensively applied in various fields, particularly in trace detection. Nevertheless, the prevailing preparation methods currently suffer from several drawbacks, including intricate preparation procedures, elevated costs, and poor stability. In this work, we center on the fabrication process of SERS substrates via femtosecond laser photoreduction. By capitalizing on the characteristics of high instantaneous power and ultra-short pulse duration of femtosecond lasers, and taking advantage of the property of the weak Raman background spectrum of the polydimethylsiloxane (PDMS) film, a high-density nanostructure with remarkable enhancement performance is formed on the film. Silver nanostructures on PDMS are characterized with scanning electron microscope (SEM). Subsequently, the optimal process parameters are deduced through the analysis of the Raman spectra of samples processed under different conditions. Additionally, the hydrophobic properties, detection stability, and sensitivity of the substrate surface are evaluated. The Raman spectral results demonstrate that the developed SERS substrate exhibits an outstanding enhancement effect, with a detection limit of 10⁻⁸ M for Rhodamine 6G (R6G). Moreover, it possesses excellent stability, with a relative standard deviation of less than 10%. In comparison with conventional methods, this approach eliminates the utilization of toxic chemical reagents and circumvents complex and time-consuming process steps, thereby offering a novel strategy for the rapid fabrication of SERS substrates.
KW - Femtosecond laser
KW - Hydrophobic
KW - photoreduction
KW - Sliver nanostructures
KW - Surface-enhanced Raman scattering
UR - https://www.scopus.com/pages/publications/105027313387
U2 - 10.1117/12.3075905
DO - 10.1117/12.3075905
M3 - Conference contribution
AN - SCOPUS:105027313387
T3 - Proceedings of SPIE - The International Society for Optical Engineering
BT - 5th International Conference on Laser, Optics, and Optoelectronic Technology, LOPET 2025
A2 - Li, Bingxiang
A2 - Costa, Manuel F. M.
PB - SPIE
Y2 - 23 May 2025 through 25 May 2025
ER -