Electrochemical Hydrogenation, Hydrogenolysis, and Dehydrogenation for Reductive and Oxidative Biomass Upgrading Using 5-Hydroxymethylfurfural as a Model System

Abstract

Ever increasing energy demands and concerns about the environment necessitate the discovery of methods for producing fuels and chemicals from renewable resources in an environmentally benign manner. Electrochemical biomass conversion is particularly promising due to the abundance of renewable biomass and the advantages of electrochemistry, including the use of renewable electricity to drive chemical reactions without consumption of additional reductants and oxidants. Biomass intermediates are chemically complex and contain multiple functional groups, requiring selective reduction or oxidation for effective biomass conversion. Reductively, controlling the selectivity between hydrogenation and hydrogenolysis is necessary for efficient reduction of oxygenated functional groups to produce desired fuels and chemicals. Oxidatively, selective dehydrogenation of a particular functional group (e.g., alcohol or aldehyde oxidation to carboxylic acid) while preventing complete oxidation to CO2 is required for conversion of biomass to value-added products. In this Perspective, we use biomass-derived 5-hydroxymethylfurfural (HMF) as an especially useful model molecule for discussing recent developments in electrochemical hydrogenation, hydrogenolysis, and dehydrogenation reactions for biomass conversion, as HMF, which contains multiple functional groups, can be transformed into various valuable chemicals by both reductive and oxidative processes. For each reaction, the electrocatalysts, reaction conditions, and mechanisms will be discussed. Through this discussion, this Perspective aims to provide researchers with a foundational understanding of electrochemical hydrogenation, hydrogenolysis, and dehydrogenation reactions that can be applied to a wide variety of organic transformations, including biomass conversion.

Halide Adsorption Enhances Electrochemical Hydrogenolysis of 5-Hydroxymethylfurfural by Suppressing Hydrogenation

“…As HAT enables only hydrogenation, suppressing HAT in acidic media can be an effective strategy to further enhance hydrogenolysis. Because Cu has been reported to be most effective for the conversion of HMF to DMF in acidic media, ,,, a special strategy that can suppress HAT on Cu in acidic media can be highly beneficial in enhancing the selectivity for DMF production.…”

Electrocatalytic Refinery of Biomass-Based 5-Hydroxymethylfurfural to Fine Chemicals

“…Biomass is a practically promising alternative to fossil fuels for the production of high-value chemicals and biofuels because it is renewable, widely distributed 4 and uses carbon feedstock from atmospheric CO 2 . 5 5-Hydroxymethylfurfural (HMF) is obtained through the dehydration of biomass-derived carbohydrates, 6 such as fructose, glucose, sucrose, cellobiose, inulin, starch, and cellulose.…”

Electrocatalytic amino acid synthesis from biomass-derivable keto acids over ball milled carbon nanotubes

“…In recent years, the electrochemical valorisation of biomass derivatives to value-added chemicals has emerged as a new frontier. [25][26][27][28][29][30][31] As an example, electrocatalytic reductive amination (ERA), occurring via the pathway shown in Scheme 1, has several advantages. Similar to other well studied electrocatalytic reactions including CO 2 /CO reduction, [32][33][34][35][36] N 2 reduction [37][38][39][40] and O 2 reduction [41][42][43] reactions, it proceeds under environmentally benign conditions, using electrons as reductants and water as the hydrogen source.…”