Plasmon-Assisted Degradation of Toxic Pollutants with Ag−AgBr/Al2O3 under Visible-Light Irradiation

• Published in: Journal of physical chemistry. C 2010-02, Vol.114 (6), p.2746-2750
• Main Authors: Zhou, Xuefeng, Hu, Chun, Hu, Xuexiang, Peng, Tianwei, Qu, Jiuhui
• Format: Article
• Language: English
• Subjects: C: Electron Transport, Optical and Electronic Devices, Hard Matter
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/jp909697k

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 highly efficient degradation of pollutants came from both photoexcited AgBr and plasmon-excited Ag NPs. Accordingly, the plasmon-induced electron-transfer processes elucidated the photostability of Ag−AgBr/MAP. These findings indicate potential applications of noble metal NPs in the fields of developing visible-light-sensitive photocatalysts and photovoltaic fuel cells.