Fabrication of surface-enhanced Raman spectroscopy substrates using silver nanoparticles produced by laser ablation in liquids

Abstract

This research describes the use of surface-enhanced Raman spectroscopy (SERS) substrates based on colloidal silver nanoparticles (AgNPs) produced by laser ablation of silver granules in pure water that are inexpensive, easy to make, and chemically stable. Here, the effects of the laser power, pulse repetition frequency, and ablation duration on the Surface Plasmon Resonance peak of AgNPs solutions, were used to determine the optimal parameters. Also, the effects of the laser ablation time on both ablation efficiency and SERS enhancement were studied. The synthesized AgNPs were characterized by UV-Vis spectrophotometer, Scanning Electron Microscope (SEM), and Raman spectrometer. The Surface Plasmon Resonance peak of AgNP solutions was centered at 404 nm confirming their synthesis and they were noted to be spherical with 34 nm in diameter. Using Raman spectroscopy, they had main bands centered at 196 cm-1 (O = Ag2/Ag-N stretching vibrations), 568 cm-1 (NH out of plane bending); 824 cm-1 (symmetric deformation of the NO2); 1060 cm-1 (NH out of plane bending); 1312 cm-1 (symmetric stretching of NO2); 1538 cm-1 (NH in-plane bending); and 2350 cm-1 (N2 vibrations). Their Raman spectral profiles remained constant within the first few days of storage at room temperature implying chemical stability. The Raman signals from blood were enhanced when mixed with AgNPs and this depended on colloidal AgNPs concentration. Using those generated by 12 h ablation time, an enhancement of 14.95 was achieved. Additionally, these substrates had an insignificant impact on the Raman profiles of samples of rat blood when mixed with them. The Raman peaks noted were attributed to CC stretching of glucose (932 cm-1); CC stretching of Tryptophan (1064 cm-1); CC stretching of β Carotene (1190 cm-1); CH2 wagging of proteins (1338 and 1410 cm-1); carbonyl stretch for proteins (1650 cm-1); CN vibrations for glycoproteins (2122 cm-1). These SERS substrates can be applied to areas such as forensics to distinguish between human and other animal blood, monitoring of the efficacy of drugs, disease diagnostics such as diabetes, and pathogen detection. All this can be achieved by comparing the Raman spectra of the biological samples mixed with the synthesized SERS substrates for different samples. Thus, the results on the use of inexpensive, simple-to-prepare Raman substrates have the possibility of making surface-enhanced Raman spectroscopy available to laboratories with scarce resources in developing nations.