Related Experiment Video
Updated: Aug 19, 2026

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Advances in Carbon-Nitrogen Bond Formation From CO2 and Nitrogenous Small Molecules Through Tandem Electrocatalysis
Arthur C Gibson1, Zhenmeng Peng2, Junhua Jiang1
1Environmental and Legacy Management Directorate, Savannah River National Laboratory, Aiken, South Carolina, USA.
Abstract:
The electrocatalytic conversion of waste product molecules to valorized chemicals and fuels driven by clean energy is a promising approach to improving environmental health and alleviating the energy crisis. Historically, emphasis has been placed on CO2 sequestration and electroreduction, as it makes up most greenhouse gas emissions, however, products obtained from CO2 reduction are limited in variety. Coupling CO2 reduction with nitrogenous small molecules (N2, NO3 -, NO2 -, etc.) would expand the variety of valorized products while simultaneously increasing the removal of harmful environmental contaminants. In this review, the benefits of tandem catalysis promoting C─N bond coupling of CO2 and nitrogenous small molecules are compared to traditional single site catalysis. Various tandem catalytic systems have been reported toward the electrosynthesis of urea, exhibiting high yield rates and extended catalytic stability. Innovative approaches have also facilitated the electrosynthesis of other organonitrogen compounds, including acetamide, methylamine, and formamide. Overall, advancements in tandem electrocatalysis signify considerable progress toward sustainable chemical synthesis, energy conservation, and emission reduction.
Related Concept Videos
Catalysis
Electrophilic Aromatic Substitution: Nitration of Benzene
Aldehydes and Ketones with Amines: Enamine Formation Mechanism
Nitrosation of Enols
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
Thermal and Photochemical Electrocyclic Reactions: Overview

