Fabrication of Gold Nanoparticles/Graphene-PDDA Nanohybrids for Bio-detection by SERS Nanotechnology

In this research, graphene nanosheets were functionalized with cationic poly (diallyldimethylammonium chloride) (PDDA) and citrate-capped gold nanoparticles (AuNPs) for surface-enhanced Raman scattering (SERS) bio-detection application. AuNPs were synthesized by the traditional citrate thermal reduc...

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Bibliographic Details
Published inNanoscale research letters Vol. 10; no. 1; p. 397
Main Authors Mevold, Andreas H H, Hsu, Wei-Wu, Hardiansyah, Andri, Huang, Li-Ying, Yang, Ming-Chien, Liu, Ting-Yu, Chan, Tzu-Yi, Wang, Kuan-Syun, Su, Yu-An, Jeng, Ru-Jong, Wang, Juen-Kai, Wang, Yuh-Lin
Format Journal Article
LanguageEnglish
Published New York Springer US 01.12.2015
Springer Nature B.V
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Summary:In this research, graphene nanosheets were functionalized with cationic poly (diallyldimethylammonium chloride) (PDDA) and citrate-capped gold nanoparticles (AuNPs) for surface-enhanced Raman scattering (SERS) bio-detection application. AuNPs were synthesized by the traditional citrate thermal reduction method and then adsorbed onto graphene-PDDA nanohybrid sheets with electrostatic interaction. The nanohybrids were subject to characterization including X-ray diffraction (XRD), transmission electron microscopy (TEM), zeta potential, and X-ray photoelectron spectroscopy (XPS). The results showed that the diameter of AuNPs is about 15–20 nm immobilized on the graphene-PDDA sheets, and the zeta potential of various AuNPs/graphene-PDDA ratio is 7.7–38.4 mV. Furthermore, the resulting nanohybrids of AuNPs/graphene-PDDA were used for SERS detection of small molecules (adenine) and microorganisms ( Staphylococcus aureus ), by varying the ratios between AuNPs and graphene-PDDA. AuNPs/graphene-PDDA in the ratio of AuNPs/graphene-PDDA = 4:1 exhibited the strongest SERS signal in SERS detection of adenine and S. aureus . Thus, it is promising in the application of rapid and label-free bio-detection of bacteria or tumor cells.
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ISSN:1931-7573
1556-276X
DOI:10.1186/s11671-015-1101-2