4.4 Article

Surface Plasmon Resonance Field-Enhanced Fluorescence Properties of Gold Quantum Dots on Polyelectrolyte Multilayers and Their H2O2 Sensor Application

期刊

PLASMONICS
卷 16, 期 4, 页码 1195-1202

出版社

SPRINGER
DOI: 10.1007/s11468-021-01388-8

关键词

Surface plasmon resonance; Layer-by-layer adsorption; Gold quantum dots; Fluorescence enhanced; Hydrogen peroxide detection; Silver nanoprisms

资金

  1. Japan Society for the Promotion of Science (JSPS) KAKENHI [JP20H02601, JP20K21140]
  2. Chiang Mai University
  3. Japanese Government (MEXT)
  4. Graduate School (Chiang Mai University)
  5. Research Center on Chemistry for Development of Health Promoting Products from Northern Resources, Center of Excellence for Innovation in Chemistry (PERCH-CIC)
  6. Center of Excellence in Materials Science and Technology, Chiang Mai University
  7. Department of Chemistry, Faculty of Science, Chiang Mai University

向作者/读者索取更多资源

The research focuses on studying surface plasmon field-enhanced fluorescence emission from gold quantum dots on an aluminum thin film coated with PDADMAC/PSS multilayers. The fluorescence intensity of the AuQDs increases as the number of PDADMAC/PSS bilayers increases, until the optimal distance between the AuQDs and the aluminum layers is reached. Additionally, the coating of silver nanoprisms onto the AuQDs allows for H2O2 sensing, with a decrease in fluorescence intensity observed due to energy transfer to the AgNPrs, and subsequent recovery upon injection of a H2O2 solution.
In this work, we investigate surface plasmon field-enhanced fluorescence (SPF) emission from gold quantum dots (AuQDs) on a polyelectrolyte multilayer ultrathin film deposited onto an Al thin film. Polyelectrolyte layers of poly(diallyl dimethyl ammonium chloride) (PDADMAC) and poly(sodium 4-styrenesulfonate) (PSS) are deposited onto the Al surface using a layer-by-layer (LbL) adsorption technique. AuQDs are subsequently deposited onto the PDADMAC/PSS ultrathin films to study their fluorescence enhancement/quenching phenomenon, as monitored by SPF spectroscopy. The distance between the AuQDs and the Al thin film is controlled by the number of deposited PDADMAC/PSS LbL films. With increasing number of the PDADMAC/PSS bilayers, the fluorescence intensity of the AuQDs increases until the optimum distance between the AuQDs and Al layers is achieved. Moreover, silver nanoprisms (AgNPrs) are coated onto the AuQDs for H2O2 sensing. When the AgNPrs are present, a decrease in the fluorescence intensity of the AuQDs due to energy transfer from the AuQDs to the AgNPrs is observed. Recovery of the fluorescence intensity of the AuQDs is observed upon injection of a H2O2 solution, where the recovery of the intensity is proportional to the H2O2 concentration in the range from 1 pM to 100 nM and results from the oxidation reaction or etching of the AgNPrs. The fluorescence recovery is attributed to weakening of the quenching effect by a reduction in concentration of the AgNPrs. The proposed system exhibits strong potential for the development of H2O2 sensors.

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