Journal
APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 215, Issue -, Pages 28-35Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2017.05.028
Keywords
Reduced TiO2; Magnesiothermic reduction; Visible light absorption; CO2 photoreduction; Stable performance
Funding
- DGIST RAMP
- D Program of the Ministry of Science, ICT AMP
- Future Planning [17-BD-0404, 17-01-HRLA-01]
- Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT AMP
- Future Planning [NRF-2015M1A2A2074670]
- Global Frontier RAMP
- D Program on Centre for Multiscale Energy System - Ministry of Education, Science and Technology of Korea [NRF-2011-0031571]
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Elevated atmospheric CO2 levels are recognized as a key driver of global warming. Making use of sunlight to photoreduce CO2, in turn fabricating hydrocarbon fuels compatible with the current energy infrastructure, is a compelling strategy to minimize atmospheric CO2 concentrations. However, practical application of such a photocatalytic system requires significant efforts for improved photoreduction performance and product selectivity. Herein, we investigate the performance of our newly developed reduced TiO2, prepared by a reduction process using Mg in 5% H-2/Ar, for photoconversion of CO2 and water vapor to hydrocarbons, primarily CH4. Using Pt nanoparticles as a co-catalyst, under simulated solar light irradiation the reduced anatase TiO2 exhibits a relatively stable performance with a threefold increase in the rate of CH4 production (1640.58 ppm g 1 h(-1), 1.13 mu mol g 1 h(-1)) as compared to anatase TiO2 nanoparticles (546.98 ppm g 1 h(-1), 0.38 mu mol g 1 h(-1)). The improved photocatalytic performance is attributed to enhanced light absorption, suitable band edge alignment with respect to the CO2/CH4 redox potential, and efficient separation of photogenerated charges. Our results suggest that the Pt-sensitized reduced TiO2 can serve as an efficient photocatalyst for solar light CO2 photoreduction. (C) 2017 Elsevier B.V. All rights reserved.
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