Stabilizing Ag Nanoparticles Using Anatase TiO2 and Cu on Al Surface

Asian Journal of Physical and Chemical Sciences

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Field Value
 
Title Stabilizing Ag Nanoparticles Using Anatase TiO2 and Cu on Al Surface
 
Creator Kaneko, Masayoshi
 
Description Chemical adsorption of anatase TiO2, silver nanoparticles (Ag NPs), and Cu particles (Cu Ps) on aluminum (Al) surface yielded an active surface-enhanced Raman scattering (SERS) substrate. TiO2 is known to reduce both silver (Ag) and copper (Cu). In an oxidizing environment, Ag NPs remain unoxidized since Cu has a more negative redox potential than Ag. Ag is therefore protected by Cu from getting oxidized. Although Ag NPs exhibit better SERS activity than Au NPs, Ag is relatively easier to oxidize, limiting the development of Ag-based nanomaterials. Therefore, despite the poor SERS activity of Au nanoparticles than that of Ag nanoparticles, Au nanoparticles have been widely used. Herein, the stabilization of Ag nanoparticles by incorporating a reductive process using anatase TiO2 is reported. The fabricated substrates bearing anatase, Ag NPs, and Cu Ps were stable, as seen by Raman spectra, and remained unchanged for more than 2 months.
 
Publisher SCIENCEDOMAIN international
 
Date 2020-11-12
 
Type info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
 
Format application/pdf
 
Identifier https://journalajopacs.com/index.php/AJOPACS/article/view/30123
10.9734/ajopacs/2020/v8i430123
 
Source Asian Journal of Physical and Chemical Sciences; 2020 - Volume 8 [Issue 4]; 22-30
2456-7779
 
Language eng
 
Relation https://journalajopacs.com/index.php/AJOPACS/article/view/30123/56518
https://journalajopacs.com/index.php/AJOPACS/article/view/30123/56519
 
Rights Copyright (c) 2020 © 2020 Kaneko; This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
 

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