Universiti Teknologi Malaysia Institutional Repository

Direct in situ activation of Ag-0 nanoparticles in synthesis of Ag/TiO2 and its photoactivity

Jaafar, N. F. and Jalil, A. A. and Triwahyono, Sugeng and Efendi, J. and Mukti, R. R. and Jusoh, R. and Che Jusoh, N. W. and Karim, A. F. and M. Salleh, N. F. and Suendo, V. (2015) Direct in situ activation of Ag-0 nanoparticles in synthesis of Ag/TiO2 and its photoactivity. Applied Surface Science, 338 . pp. 75-84. ISSN 0169-4332

Full text not available from this repository.

Official URL: http://doi.org/10.1016/j.apsusc.2015.02.106


Metallic Ag nanoparticles (Ag0) were successfully activated using a direct in situ electrochemical method before being supported on TiO2. Catalytic testing showed that 5 wt% Ag–TiO2 gave the highest photodegradation (94%) of 50 mg L-1 2-chlorophenol (2-CP) at pH 5 using 0.375 g L-1 catalyst within 6 h, while under similar conditions, 1 wt% and 10 wt% Ag–TiO2 only gave 75% and 78% degradation, respectively. Characterization results illustrated that the photoactivity was affected by the amount of Ag0 and oxygen vacancies which act as an electrons trap to enhance the electron–hole separation. While, the Agsingle bondOsingle bondTi bonds formation reduced the photoactivity. The degradation followed a pseudo-first order Langmuir–Hinshelwood model where adsorption was the controlling step. Study on the effect of scavengers showed that the hole (H+) and hydroxyl radical (OHradical dot) play important roles in the photodegradation. The regenerated photocatalyst was still stable after five cycling runs.

Item Type:Article
Uncontrolled Keywords:ag–tio2 catalyst, electrochemical, electron–hole pairs separation, photodegradation, 2-chlorophenol
Subjects:A General Works
ID Code:58313
Deposited By: Haliza Zainal
Deposited On:04 Dec 2016 12:07
Last Modified:18 Apr 2017 09:39

Repository Staff Only: item control page