Journal
SCIENCE CHINA-CHEMISTRY
Volume 65, Issue 12, Pages 2588-2595Publisher
SCIENCE PRESS
DOI: 10.1007/s11426-022-1407-0
Keywords
biomass conversion; electrocatalytic hydrogenation; furfural; CuO; synergistic effect
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Funding
- National Key R&D Program of China [2020YFA0710000]
- National Natural Science Foundation of China [22122901, 21902047, 21825201, U19A2017]
- Provincial Natural Science Foundation of Hunan [2020JJ5045, 2021JJ20024, 2021RC3054]
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This study reveals the active oxidation state of Cu-based catalysts for the electrochemical hydrogenation of furfural and confirms the co-existence of Cu+ and Cu-0 on the catalyst surface. Furthermore, it demonstrates the crucial role of Cu+ in the reaction, and the density functional theory calculations suggest that the synergistic effect of Cu-0 and Cu+ is beneficial for both kinetics and thermodynamics.
Electrochemical hydrogenation (ECH) of furfural, which uses the proton from water and avoids the usage of gaseous hydrogen and high pressure, is an efficient way to utilize biomass energy. Cu-based catalysts are promising catalysts for the ECH of furfural. However, their active sites and reaction mechanism have not been fully understood yet. This work unveils the active oxidation state of Cu-based electrocatalysts for the ECH of furfural. The co-existence of Cu+ and Cu-0 on the CuO surface under the working potential is confirmed by a series of in situ characterizations. The poisoning experiment shows that the performance decreased heavily after the Cu+ was complexed with SCN-, indicating the decisive role of Cu+. Finally, the density functional theory (DFT) calculation suggests that the Cu-0-Cu+ synergistic effect is beneficial to both kinetics and thermodynamics: Cu+ accelerates the second step hydrogenation process of furfural, and Cu-0 reduces the energy barrier for the desorption of furfuryl alcohol. This work demonstrates the synergistic effect of Cu-0 and Cu+ states for the electrochemical hydrogenation of furfural and provides a deeper understanding of the furfural hydrogenation mechanism.
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