4.7 Article

Bimetallic AgNPs@dopamine modified-halloysite nanotubes-AuNPs for adenine determination using surface-enhanced Raman scattering

期刊

MICROCHIMICA ACTA
卷 188, 期 4, 页码 -

出版社

SPRINGER WIEN
DOI: 10.1007/s00604-021-04778-1

关键词

Halloysitenanotube; Surface-enhanced Raman scattering (SERS); Rapid analysis; Adenine; Complex sample matrix

资金

  1. Research and Development Plan for Key Areas of Food Safety in Guangdong Province of China [2019B020211001]
  2. National Key Research and Development Program of China [2019YFC1606101]
  3. National Natural Science Foundation of China [21775167, 21976213]

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A bimetallic nanoparticles modified halloysite nanotubes hybrid with enhanced surface-enhanced Raman scattering (SERS) ability was prepared by embedding AgNPs and modifying AuNPs on dopamine-modified HNTs, leading to a sensitive and reproducible substrate for adenine determination.
A bimetallic nanoparticles modified halloysite nanotubes (HNTs) hybrid was prepared by embedding AgNPs and modifying AuNPs on the inner or outer wall of dopamine-modified HNTs (DHNTs) in sequence. The resulting bimetallic AgNPs@DHNTs-AuNPs hybrid as surface-enhanced Raman scattering (SERS) substrate exhibited improved enhancement ability over monometallic AgNPs@DHNTs, and DHNTs-AuNPs substrates, with intensity ratios of about 48:1:9 (crystal violet) and 11:1:2 (p-phenylenediamine). The giant SERS effect of AgNPs@DHNTs-AuNPs substrate is probably attributed to the synergetic enhancement of the electromagnetic field (Au/Ag), optical plasmon force, molecular enrichment (HNTs), and charge transfer (NPs-dopamine-molecules). The sensitive and reproductive AgNPs@DHNTs-AuNPs substrate was applied for SERS determination of adenine with a linear range of 0.010-0.50 mg.L-1 and a detection limit of 2.2 mu g.L-1. The SERS method enables the rapid determination of adenine in fish, chicken kidney and heart, and serum samples, with recoveries of 83.5-121.6% and relative standard deviations of 2.5-7.9%. The SERS substrate has high value for rapid analysis of food and biomarker determinations.

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