Diatomic molecule

Engineering

Faraday efficiency

Coupling (piping)

Yield (engineering)

Physical chemistry

Embedded system

Adsorption

Catalysis

Electrode

Organic chemistry

Inorganic chemistry

Chemistry

Metallurgy

Materials science

Urea

Molecule

Computer science

Chemical engineering

Electrochemistry

Atom (system on chip)

Nature Communications

Electrocatalytic urea synthesis emerged as the promising alternative of Haber–Bosch process and industrial urea synthetic protocol. Here, we report that a diatomic catalyst with bonded Fe–Ni pairs can significantly improve the efficiency of electrochemical urea synthesis. Compared with isolated diatomic and single-atom catalysts, the bonded Fe–Ni pairs act as the efficient sites for coordinated adsorption and activation of multiple reactants, enhancing the crucial C–N coupling thermodynamically and kinetically. The performance for urea synthesis up to an order of magnitude higher than those of single-atom and isolated diatomic electrocatalysts, a high urea yield rate of 20.2 mmol h−1 g−1 with corresponding Faradaic efficiency of 17.8% has been successfully achieved. A total Faradaic efficiency of about 100% for the formation of value-added urea, CO, and NH3 was realized. This work presents an insight into synergistic catalysis towards sustainable urea synthesis via identifying and tailoring the atomic site configurations. The direct electrocatalytic synthesis of urea via C–N coupling is of great significance. The authors report a diatomic catalyst with bonded Fe–Ni pairs to improve the efficiency of electrochemical urea synthesis from nitrate and CO2.

Identifying and tailoring C–N coupling site for efficient urea synthesis over diatomic Fe–Ni catalyst