“…There remains a debate, however, as to whether these steps occur through an electrochemical hydrogenation (ECH) pathway or through a proton-coupled electron transfer (PCET) pathway . While the first report on the electrocatalytic reduction of FAL dates back to 1939, it has gained a renewed and rapidly growing interest over the past decade and has been the object of several recent perspective and review articles. − Early studies described the electrochemical reduction of FAL in aqueous media (sometimes containing methanol) inside H-cell setups, on a range of metal electrodes – Pt, Ni, Cu, Al, and stainless steel. − Conversely, in more recent studies, Cu has been mostly favored due to its superior activity and selectivity. ,− These works collectively show that, on bare copper, FAL is preferentially converted to FOH under neutral conditions, at applied potentials more negative than −0.5 V vs RHE, while 2-MF is the main product under highly acidic conditions at potentials more negative than −0.45 V vs RHE (see Table S3 for a collection of recent data from the literature). In these studies, the concentration of FAL was in the 0.01–0.1 M range, with the appearance of hydrofuroin as a secondary product at higher concentrations.…”