Highly Efficient Electrosynthesis of Glycine over an Atomically Dispersed Iron Catalyst

Abstract

Glycine is a nonessential amino acid that plays a vital role in various biological activities. However, the conventional synthesis of glycine requires sophisticated procedures or toxic feedstocks. Herein, we report an electrochemical pathway for glycine synthesis via the reductive coupling of oxalic acid and nitrate or nitrogen oxides over atomically dispersed Fe–N–C catalysts. A glycine selectivity of 70.7% is achieved over Fe–N–C-700 at −1.0 V versus RHE. Synergy between the FeN 3 C structure and pyrrolic nitrogen in Fe–N–C-700 facilitates the reduction of oxalic acid to glyoxylic acid, which is crucial for producing glyoxylic acid oxime and glycine, and the FeN 3 C structure could reduce the energy barrier of *HOOCCH 2 NH 2 intermediate formation thus accelerating the glyoxylic acid oxime conversion to glycine. This new synthesis approach for value-added chemicals using simple carbon and nitrogen sources could provide sustainable routes for organonitrogen compound production.