Efficient photocatalytic hydrogen generation by silica supported and platinum promoted titanium dioxide
- 1. Environmental Materials Division, National Environmental Engineering Research Institute (NEERI, C.S.I.R.), Nagpur 440020 (India)
- 2. Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur 440010 (India)
Description
Graphical abstract: Titanium dioxide was supported on mesoporous silica and promoted with Pt and Ru. The supported photocatalysts show high surface area and better photocatalytic activity in visible light as compared to the benchmark Degussa P25. These photocatalysts were characterized using XRD, BET-SA, and UV-DRS techniques. The surface area of supported photocatalyst was 140.6 m2/g which is higher than Degussa P-25. Supported photocatalyst was evaluated for hydrogen evolution via water splitting reaction using ethanol as a sacrificial donor. Hydrogen yield observed is 4791.43 μmol/h/g of TiO2 and that for P-25 is 161 μmol/h/g of TiO2 under visible light irradiation. The value is 30 times higher than benchmark material Degussa P-25. This photocatalyst is also found stable up to 24 h without replenishing with sacrificial donor ethanol. - Highlights: • Semiconductor titanium dioxide has been supported on silica gel and promoted with Pt by simple wet impregnation route. • This synthesized photocatalyst is showing high surface area of 140.6 m2/g with crystallite size in the range of 15.44 Å. • This photocatalyst is showing enhanced hydrogen yield of about 4791.43 μmol/h/g of TiO2. • This photocatalyst is also found stable up to 24 h without replenishing with sacrificial donor ethanol. • The effect of various operating parameters on supported photocatalyst also has been studied. - Abstract: Titanium dioxide was supported on mesoporous silica and promoted with Pt and Ru. The supported photocatalysts show high surface area and better photocatalytic activity in visible light as compared to the benchmark Degussa P25. These photocatalysts were characterized using XRD, BET-SA, and UV-DRS techniques. The surface area of supported photocatalyst was 140.6 m2/g which is higher than Degussa P-25. Supported photocatalyst was evaluated for hydrogen evolution via water splitting reaction using ethanol as a sacrificial donor. Hydrogen yield observed is 4791.43 μmol/h/g of TiO2 and that for P-25 is 161 μmol/h/g of TiO2 under visible light irradiation. The value is 30 times higher than benchmark material Degussa P-25. This photocatalyst is also found stable up to 24 h without replenishing with sacrificial donor ethanol. However silica gel/TiO2/Ru does not show any exciting result for hydrogen generation. The effect of various operating parameters like photocatalyst loading, Illumination time and intensity of light on supported photocatalyst also has been studied
Availability note (English)
Available from http://dx.doi.org/10.1016/j.materresbull.2013.05.057Additional details
Identifiers
- DOI
- 10.1016/j.materresbull.2013.05.057;
- PII
- S0025-5408(13)00436-4;
Publishing Information
- Journal Title
- Materials Research Bulletin
- Journal Volume
- 48
- Journal Issue
- 9
- Journal Page Range
- p. 3545-3552
- ISSN
- 0025-5408
- CODEN
- MRBUAC
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46048118
- Subject category
- S36: MATERIALS SCIENCE; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- ETHANOL; HYDROGEN; INTERSTITIAL HYDROGEN GENERATION; IRRADIATION; NANOSTRUCTURES; PHOTOCATALYSIS; PLATINUM; SILICA; SILICA GEL; SOL-GEL PROCESS; TITANIUM OXIDES; X-RAY DIFFRACTION
- Descriptors DEC
- ADSORBENTS; ALCOHOLS; CATALYSIS; CHALCOGENIDES; COHERENT SCATTERING; DIFFRACTION; ELEMENTS; HYDROXY COMPOUNDS; METALS; MINERALS; NONMETALS; ORGANIC COMPOUNDS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHYSICAL RADIATION EFFECTS; PLATINUM METALS; RADIATION EFFECTS; SCATTERING; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.