Plasmon-Assisted Degradation of Toxic Pollutants with Ag−AgBr/Al2O3 under Visible-Light Irradiation
Author(s) -
Xuefeng Zhou,
Chun Hu,
Xuexiang Hu,
Tianwei Peng,
Jiuhui Qu
Publication year - 2010
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/jp909697k
Subject(s) - photocatalysis , photochemistry , surface plasmon resonance , visible spectrum , excited state , materials science , mesoporous material , plasmon , nanoparticle , silver nanoparticle , chemistry , nanotechnology , catalysis , optoelectronics , organic chemistry , nuclear physics , physics
AgBr coated with silver (Ag) nanoparticles (NPs) were highly dispersed on ordered mesoporous γ-Al2O3 (MA) by the deposition−precipitation method with surfactant (Ag−AgBr/MAP). The catalyst showed high and stable photocatalytic activity for the degradation and mineralization of toxic persistent organic pollutants, as demonstrated with 2-chlorophenol (2-CP), 2,4-dichlorophenol, and trichlorophenol under visible light or simulated solar light irradiation. The dispersion of Ag−AgBr NPs on MA strongly affected their photoactivity. On the basis of electron spin resonance and cyclic voltammetry analyses under a variety of experimental conditions, two plasmon-induced electron-transfer processes were verified from the excited Ag NPs to AgBr and from 2-CP to the Ag NPs, resulting in O2•− and excited h+ on Ag NPs. Also, •OH and O2•− were formed by photoexcited AgBr. Both •OH and O2•− radicals were primary active species, whereas the excited h+ on Ag NPs was involved in the photoreaction system of Ag−AgBr/MAP. The hi...
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