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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Wu, Ling Fu, Xianzhi Li, Danzhen Chen, Yilin Wang, Xuxu Wang, Xinchen |
| Copyright Year | 2005 |
| Abstract | Superior photocatalytic activity and durability of Pt/TiO2 for decomposing volatile organic pollutants (typically aromatic compounds) have been obtained by adding trace H2 into an O2-rich photooxidation system. The order of photodegradation efficiencies for volatile organic compounds is cyclohexane < acetone < benzene < toluene < ethylbenzene. Exceptional stability of Pt/TiO2 for benzene photodegradation is still maintained after 22 h of testing, by the repeated use of the catalyst four times. The promoting effects of H2 in the photocatalysis were studied by infrared spectroscopy (IR), spin-trapping electron paramagnetic resonance (EPR) and surface photovoltage spectroscopy (SPS). Results demonstrated that the introduced H2 has several beneficial effects on heterogeneous photocatalysis, namely, a comparatively clean surface of Pt/TiO2 with no persistent aromatic intermediates, an increased number of surface hydroxyl radicals in the photocatalytic process, and an enhanced separation efficiency of photogenerated electron–hole pairs. A mechanism is proposed to elucidate the promoting effect of H2 on the photooxidation of volatile organic pollutants over Pt/TiO2. |
| Starting Page | 1514 |
| Ending Page | 1519 |
| Page Count | 6 |
| File Format | HTM / HTML PDF |
| ISSN | 11440546 |
| Volume Number | 29 |
| Issue Number | 12 |
| Journal | New Journal of Chemistry |
| DOI | 10.1039/b510953a |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Subscribed |
| Subject Keyword | Photodegradation Infrared spectroscopy Spectroscopy Oxygen EPR Toluene Photocatalysis Volatile organic compound Ethylbenzene Surface photovoltage Benzene Cyclohexane Electron paramagnetic resonance Hydroxyl radical Acetone |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Materials Chemistry Catalysis |
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