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Visible-light-driven conversion of CO to CO and high-value-added carbon products is a promising strategy for mitigating CO emissions and reserving solar energy in chemical form. We report an efficient system for CO transformation to CO catalyzed by bare CoP, hybrid CoP/carbon nanotubes (CNTs), and CoP/reduced graphene oxide (rGO) in mixed aqueous solutions containing a Ru-based photosensitizer, under visible-light irradiation. The in situ prepared hybrid catalysts CoP/CNT and CoP/rGO show excellent catalytic activities in CO reduction to CO, with a catalytic rates of up to 39 510 and 47 330 μmol h g in the first 2 h of reaction, respectively; a high CO selectivity of 73.1 % for the former was achieved in parallel competing reactions in the photoreduction of CO and H O. A combination of experimental and computational studies clearly shows that strong interactions between CoP and carbon-supported materials and partially adsorbed H O molecules on the catalyst surface significantly improve CO-generating rates.
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http://dx.doi.org/10.1002/chem.201800335 | DOI Listing |
Chemistry
March 2018
Key Laboratory of Photochemical Conversion and Optoelectronic, Materials and HKU-CAS Joint Laboratory on New Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
Visible-light-driven conversion of CO to CO and high-value-added carbon products is a promising strategy for mitigating CO emissions and reserving solar energy in chemical form. We report an efficient system for CO transformation to CO catalyzed by bare CoP, hybrid CoP/carbon nanotubes (CNTs), and CoP/reduced graphene oxide (rGO) in mixed aqueous solutions containing a Ru-based photosensitizer, under visible-light irradiation. The in situ prepared hybrid catalysts CoP/CNT and CoP/rGO show excellent catalytic activities in CO reduction to CO, with a catalytic rates of up to 39 510 and 47 330 μmol h g in the first 2 h of reaction, respectively; a high CO selectivity of 73.
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