Electrosynthesis of Amino Acids from Biomass and Nitrate at Industrial Current Densities Using Porous PbBi Electrodes

Electrosynthesis is a rising and attractive method for efficient amino acid production. However, industrial-grade electrosynthesis of high-value amino acids from simple carbon and nitrogen substrates is confronted with a great challenge. Herein, we design a dual-site PbBi alloy catalyst for various amino acids' electrosynthesis from keto acids and nitrate. An alanine Faradaic efficiency of 59.7% is delivered at −1.5 V vs SCE, reaching the industrial current density of 570 mA cm–2 with high catalytic durability of the porous Pb1Bi0.1 catalyst. In the tandem reaction process, nitrate is first converted to NH2OH via electrochemical reduction mainly over the Bi site. Then the obtained NH2OH integrates with the α-keto acid to form the oxime intermediate. Lastly, the Pb site facilitates the electroreduction of oxime to the final amino acids. More importantly, over 10 kinds of α-amino acids can be successfully synthesized in excellent FE and high yield at high current density, indicating the superior catalytic activity and wide universality of our strategy. In short, this work opens up a novel approach to realize the one-pot electrosynthesis of various amino acids from renewable biomass feedstocks and nitrate waste industrially.