Published September 15, 2015 | Version v1
Journal article

Plasma-induced formation of flower-like Ag2O nanostructures

Description

Graphical abstract: Flower-like Ag2O nanostructures. - Highlights: • Flower-like Ag2O nanostructures were synthesized from Ag colloids using plasma. • XPS was used to monitor plasma treatment effect on Ag colloids. • SERS of methyl orange was used to monitor the plasma oxidation–reduction processes. • Photocatalytic degradation of methylene blue was performed using Ag2O. • Ag2O is a more efficient visible light photocatalyst than Ag colloids. - Abstract: Plasma treatment effect on Ag colloids was investigated using X-ray photoelectron spectroscopy (XPS) and surface-enhanced Raman scattering (SERS) techniques. XPS showed that O2 plasma was critical in removing organic residues in Ag colloids synthesized using citric acid as a reducing agent. With O2 plasma treatment, Ag colloids were also oxidized to form flower-like Ag2O nanostructures. The formation mechanism is proposed. The SERS spectral intensity of methyl orange (MO) adsorbed on Ag surface became deteriorated with O2 plasma treatment. Followed by H2 plasma treatment, the SERS intensity of MO on Ag regained, which indicated that Ag2O has been reduced to Ag. Nonetheless, the reduction by H2 plasma could not bring Ag back to the original as-synthesized nanoparticle morphology. The flower-like nanostructure morphology still remained. The photocatalytic degradation reactions of methylene blue (MB) aqueous solutions were carried out using Ag colloids and Ag2O nanostructures. The results show that Ag2O is more efficient than Ag colloids and many other metal oxides for the photocatalytic degradation of MB in solution when utilizing visible light

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2015.05.055

Additional details

Identifiers

DOI
10.1016/j.apsusc.2015.05.055;
PII
S0169-4332(15)01173-3;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
349
Journal Page Range
p. 609-614
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.