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Solar Hydrogen Production Coupled with the Degradation of a Dye Pollutant Using TiO2 Modified with Platinum and Nafion

Title
Solar Hydrogen Production Coupled with the Degradation of a Dye Pollutant Using TiO2 Modified with Platinum and Nafion
Author(s)
Kim, JungwonPark, YiseulPark, Hyunwoong
Issued Date
2014-10
Citation
International Journal of Photoenergy, v.2014
Type
Article
Keywords
ESTROGENIC ACTIVITY REMOVALVISIBLE-LIGHT IRRADIATIONLOW-COST ADSORBENTSEOSIN YSENSITIZED TIO2COATED TIO2RHODAMINE-BNANOPARTICLESEVOLUTIONACID
ISSN
1110-662X
Abstract
The simultaneous production of molecular hydrogen (H2) and degradation of rhodamine B (RhB) was successfully achieved using TiO2 modified with platinum and nafion (Pt/TiO2/Nf) under visible light ( > 420 nm). Pt/TiO2/Nf exhibited high activity for H2 production in the presence of RhB and EDTA as a photosensitizer (also an organic dye pollutant) and an electron donor, respectively. However, the activity of TiO2 modified with either platinum or nafion for H2 production was negligible under the same experimental conditions. The negatively charged nafion layer enhances the adsorption of cationic RhB and pulls protons, a source of hydrogen, to the surface of TiO2 through electrostatic attraction. On the other hand, platinum deposits on TiO2 can act as an electron sink and a temporary electron reservoir for the reduction of protons. With the production of H2, RhB was gradually degraded through N -deethylation, which was confirmed by the spectral blue shift of the maximum absorption wavelength ( m a x) from 556 to 499 nm (corresponding to the m a x of rhodamine 110). With Pt/TiO2/Nf employed at [ RhB ] = 20 M (0.6 mol), approximately 70 mol of H2 was produced and RhB and its intermediates were completely removed over a 12 h period. A detailed reaction mechanism was discussed. © 2014 Jungwon Kim et al.
URI
http://hdl.handle.net/20.500.11750/2407
DOI
10.1155/2014/324859
Publisher
Hindawi Publishing Corporation
Files in This Item:
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Appears in Collections:
Smart Textile Convergence Research Group 1. Journal Articles

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