Abstract
The electrocatalytic reduction of 5-hydroxymethylfurfural (HMF) is highly selective to 2,5-bishydroxymethylfuran (BHMF) at pH=9.2, diluted HMF solutions, and low current densities. In this work, the electrochemical reduction of 0.05 m HMF solutions was investigated in the 5-50 mA cm-2 current density range over an AgCu foam electrocatalyst. The selectivity towards the formation of BHMF or the dimerization depended on the current density, likely due to differences in the electrode potential, and on the reaction time. Operating at current densities of 40-50 mA cm-2 allowed to find a trade-off between HMF and H2 O activation, achieving 85 % BHMF selectivity and fostering the productivity (0.567 mmol cm-2 h-1 ), though co-producing H2 . The electrochemical characterization by Tafel slopes and electrochemical impedance spectroscopy indicated that the HMF reduction was kinetically favored in comparison to the hydrogen evolution reaction and that the process was limited by charge transfer.