Structure sensitivity of the electrochemical hydrogenation of cis,cis-muconic acid to hexenedioic acid and adipic acid

Abstract

The global market of fossil carbon-derived adipic acid (AA) was over 3 million tons in 2022, emitting 3.1 million tons of the potent greenhouse gas N₂O. Alternative biomass-derived feedstocks offer a sustainable option to replace fossil carbon, but alternative pathways for AA synthesis are also required to curb the substantial emissions associated with the process. A novel and sustainable approach to synthesize AA is by coupling biomanufacturing and electrocatalysis. Biologically-produced cis,cis-muconic acid (ccMA) from sugars and lignin monomers has recently gained significant attention as a precursor to AA, as it can be electrochemically hydrogenated to AA using water-derived (instead of fossil-derived) hydrogen and electricity generated from wind energy. For the first time in literature, we demonstrate appreciable electrochemical production of AA using supported palladium nanoparticles. The performance of this system contrasts with that of palladium foil or platinum-based catalysts, which produced little AA. Density functional theory calculations on model surfaces of palladium and platinum suggest that the reduction of ccMA to trans-3-hexenedioic acid occurs through an outer sphere proton-coupled electron transfer mechanism, while subsequent reduction to AA preferentially occurs on surface terrace sites. Our calculations also explain the exceptional performance of palladium nanoparticles compared to palladium- and platinum-based foils, attributing the more favorable activation energy barriers found on palladium terraces to the relatively moderate binding strength of adsorbed species. These results suggest structure-sensitive catalyst design strategies that maximize the exposure of terrace atoms for further improvement of the ccMA electrochemical hydrogenation process.