The development of industry and the increase in population have caused energy shortages and environmental pollution problems. Developing clean and storable new energy is identified as a key way to solve the problems above. Hydrogen is viewed as th...
CO2 Reduction Mechanism on the Cu2O(110) Surface: A First‐Principles Study
Von Wiley-VCH zur Verfügung gestellt
The ideal Cu2O(110) surface is the most active and selective for CO2 reduction to methanol. The Cu(0) at O vacancy and Cu/Cu2O interface promotes the adsorption and activation of CO2, but the removal of residual O becomes potential-limiting. With increasing degrees of reduction, the activity and selectivity of the surface vary.
Cu2O is an attractive catalyst for the selective reduction of CO2 to methanol. However, the mechanism of the reaction and the role of the Cu species in different oxidation states are not well understood yet. In this work, by first-principles calculations, we investigate the mechanism of the reaction on the Cu2O(110) surface, which is the most selective for methanol, in different degrees of reduction: ideal surface, slightly reduced surface (SRS), and partially reduced surface (PRS). The most favorable reaction pathways on the three surfaces were identified. We found that Cu(I) on the ideal surface is not capable of chemisorbing CO2, but surface oxygen serves as the active site which selectively converts CO2 to CH3OH with a limiting potential of −0.77 V. The Cu(0) on the SRS and PRS promotes the adsorption and reduction of CO2, while the removal of the residue O* becomes potential/rate limiting with a more negative limiting potential than the ideal surface. The SRS is selective to methanol while the PRS becomes selective to methane. The result suggests that the key to high methanol selectivity is to avoid the reduction of Cu(I), which provides a new strategy for the design of more efficient catalysts for selective CO2 reduction to methanol.Zum Volltext
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