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. 2022 Sep 5;12(17):3080.
doi: 10.3390/nano12173080.

Detailed Investigation of Factors Affecting the Synthesis of SiO2@Au for the Enhancement of Raman Spectroscopy

Affiliations

Detailed Investigation of Factors Affecting the Synthesis of SiO2@Au for the Enhancement of Raman Spectroscopy

Nguyen Thi Phuong Thao et al. Nanomaterials (Basel). .

Abstract

The reaction time, temperature, ratio of precursors, and concentration of sodium citrate are known as the main factors that affect the direct synthesis process of SiO2@Au based on the chemical reaction of HAuCl4 and sodium citrate. Hence, we investigated, in detail, and observed that these factors played a crucial role in determining the shape and size of synthesized nanoparticles. The significant enhancement of the SERS signal corresponding to the fabrication conditions is an existing challenge. Our study results show that the optimal reaction conditions for the fabrication of SiO2@Au are a 1:21 ratio of HAuCl4 to sodium citrate, with an initial concentration of sodium citrate of 4.2 mM, and a reaction time lasting longer than 6 h at a temperature of 80 °C. Under optimal conditions, our synthesis process result is SiO2@Au nanoparticles with a diameter of approximately 350 nm. In particular, the considerable enhancement of Raman intensities of SiO2@Au compared to SiO2 particles was examined.

Keywords: Raman spectroscopy; SERS; SiO2@Au; core shell.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Scheme 1
Scheme 1
Process of preparing SiO2@Au material.
Figure 1
Figure 1
Pictures of samples at different temperatures (a). UV-Vis spectra of samples at different temperatures (b) and their UV-Vis baseline spectra (c).
Figure 1
Figure 1
Pictures of samples at different temperatures (a). UV-Vis spectra of samples at different temperatures (b) and their UV-Vis baseline spectra (c).
Figure 2
Figure 2
Pictures of samples at different reaction times (a). UV-Vis spectra of samples at different reaction times (b) and their UV-Vis baseline spectra (c).
Figure 2
Figure 2
Pictures of samples at different reaction times (a). UV-Vis spectra of samples at different reaction times (b) and their UV-Vis baseline spectra (c).
Figure 3
Figure 3
Pictures of samples at different ratios of HAuCl4 to sodium citrate (a). UV-Vis spectra of samples at different ratios of HAuCl4 to sodium citrate (b) and their UV-Vis baseline spectra (c).
Figure 3
Figure 3
Pictures of samples at different ratios of HAuCl4 to sodium citrate (a). UV-Vis spectra of samples at different ratios of HAuCl4 to sodium citrate (b) and their UV-Vis baseline spectra (c).
Figure 4
Figure 4
Pictures of samples at different concentrations of sodium citrate (a). UV-Vis spectra of samples at different concentrations of sodium citrate (b) and their UV-Vis baseline spectra (c). N1: 0.21 mM; N2: 0.42 mM; N3: 0.84 mM; N4: 1.5 mM; N5: 4.2 mM.
Figure 5
Figure 5
Pictures of SiO2, SiO2@PEI, AuNPs, and SiO2@Au synthesized under optimal conditions (a). UV-Vis spectra of SiO2, SiO2@PEI, AuNPs, and SiO2@Au synthesized under optimal conditions (b) and their UV-Vis baseline spectra (c).
Figure 6
Figure 6
SEM images of SiO2 (a), SiO2@PEI (b), and SiO2@Au (c).
Figure 6
Figure 6
SEM images of SiO2 (a), SiO2@PEI (b), and SiO2@Au (c).
Figure 7
Figure 7
Dynamic Light Scattering results of SiO2 (a) and SiO2@Au (b).
Figure 8
Figure 8
Raman spectra of methylene blue solution deposited on SiO2 and SiO2@Au.

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