Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 43, Pages 21596-21604Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta08091g
Keywords
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Funding
- NSFC of China [21671034, 21471027]
- Fundamental Research Funds for the Central Universities [2412016KJ041]
- Changbai Mountain Scholars of Jilin Province
- Foundation of Jilin Educational Committee [2016498]
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The photoreduction of CO2 to CO offers a promising sustainable and clean approach for a global new energy program. Coupling this reductive process with a matched water photo-oxidation pathway is an attractive avenue to accelerate the half-reaction of CO2 reduction. Herein, we propose a three-component photocatalyst design strategy for reducing CO2 to CO coupled with water oxidation via a two-electron/two-step pathway. Employing polyoxotitanium ([Ti17O24(OPri)(20)]) as a titanium source, ultrasmall TiO2-x nanoparticles coated with ultrathin carbon layers (C-TiO2-x) were fabricated and loaded on to a g-C3N4 matrix through chemical bonding (C-TiO2-x@g-C3N4) for the first time. The optimized C-TiO2-x@g-C3N4 photocatalyst showed a very high activity of 12.30 mmol g(-1) (204.96 mmol g(TiO2)(-1)) CO generation within 60 h visible-light irradiation, which represents the highest CO production rate to date among the reported TiO2-based materials under similar conditions. The excellent adsorption capability of C-TiO2-x@g-C3N4 for photons, H+ protons, and CO2 molecules together with efficient charge separation and the two-electron/two-step oxidative pathway lead to the high reactivity.
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