Loading…
Enhanced Photodegradation of Toxic Pollutants on Plasmonic Au–Ag–AgI/Al2O3 Under Visible Irradiation
Au–Ag–AgI nanoparticles (NPs) were uniformly dispersed onto mesoporous alumina by deposition–precipitation and photoreduction at low temperature. Compared with Ag–AgI/Al 2 O 3 , the catalyst showed higher photocatalytic activity under visible irradiation. In particular, the release of metal ions fro...
Saved in:
Published in: | Catalysis letters 2012-05, Vol.142 (5), p.646-654 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Au–Ag–AgI nanoparticles (NPs) were uniformly dispersed onto mesoporous alumina by deposition–precipitation and photoreduction at low temperature. Compared with Ag–AgI/Al
2
O
3
, the catalyst showed higher photocatalytic activity under visible irradiation. In particular, the release of metal ions from the catalyst was significantly inhibited during photodegradation of pollutants. Electron spin resonance and cyclic voltammograms studies under a variety of experimental conditions verified that the coupling of Au and Ag NPs increased the efficiency of light energy conversion and accelerated interfacial electron transfer processes. The main active species involved in the photoreaction of Au–Ag–AgI/Al
2
O
3
were O
2
•−
and excited h
+
on the metal NPs. The presence of several ubiquitous anions, including HCO
3
−
, SO
4
2−
, and NO
3
−
could act as electron donors trapping excited h
+
on the metal NPs to facilitate electron circulation. The results obtained herein indicated that coupled, noble, bimetal NPs exhibited high photosensitivity and photostability due to enhanced surface plasmon resonance and interfacial electron transfer.
Graphical Abstract
Addition of Au made Au–Ag–AgI nanoparticles (NPs) disperse more uniformly onto mesoporous Al
2
O
3
and showed higher photocatalytic activity under visible irradiation. |
---|---|
ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-012-0788-2 |