Converting biomass-derived 5-hydroxymethylfurfural (HMF) into high-valued 2,5-dihydroxymethylfurfural (DHMF) via electrocatalytic hydrogenation (ECH) technology has been widely regarded as one of the most economical and eco-friendly routes. The high selectivity and activity depend on the reasonable regulation of the adsorption and activation of adsorbed hydrogen (H*) and HMF on the surface of the electrocatalyst. Herein, we report nanoflower-like CuFe-based electrocatalysts on copper foam (CF) substrates (CuFeO/CF). DHMF was achieved on the optimal CuFeO/CF with a selectivity of 93.3 % and a yield of 90.1 %. The H*, HMF and product were observed by in situ attuned total reflection Fourier transform infrared spectroscopy (ATR-FTIR). Moreover, in situ Raman spectra discloses the reconstruction of catalyst into CuFe-bimetal with low valence state. Density functional theory (DFT) calculations demonstrate that introducing Fe plays a role in regulating the electronic structure of Cu sites, which facilitate the generation of H* and adsorption of HMF, thus hampering the occurrence of dimerization. This study provides an innovative idea for the rational design of non-precious bimetallic electrocatalysts for ECH to produce high-valued chemicals.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11696196 | PMC |
http://dx.doi.org/10.1002/cssc.202401278 | DOI Listing |
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