Boosting Electrocatalytic
Nitrate Reduction to Ammonia
on a Hierarchical Nanoporous Ag,Ni-Codoped Cu Catalyst via Trimetallic
Synergistic and Nanopore Enrichment Effects
The electrochemical nitrate (NO<sub>3</sub><sup>–</sup>)
reduction reaction (NO<sub>3</sub><sup>–</sup>RR) offers a
promising route for NO<sub>3</sub><sup>–</sup> wastewater treatment
and sustainable ammonia (NH<sub>3</sub>) synthesis. However, the reaction
still faces the challenges of unsatisfactory productivity and selectivity.
Herein, we report a hierarchical nanoporous Ag,Ni-codoped Cu (np Ag,Ni-Cu)
catalyst that exhibits a high NH<sub>3</sub> Faradaic efficiency of
98.5% with an attractive NH<sub>3</sub> yield rate of 41.1 mg h<sup>–1</sup> mg<sub>cat</sub><sup>–1</sup> at −0.2
V vs RHE for the NO<sub>3</sub><sup>–</sup>RR. Density functional
theory calculations and molecular dynamics simulations suggest that
the excellent performance of np Ag,Ni-Cu results from a trimetallic
synergistic effect and nanopore enrichment/confinement effect, in
which the codoping of Ni and Ag into Cu can enhance NO<sub>3</sub><sup>–</sup> adsorption, prevent *NO<sub>2</sub> desorption,
and suppress the hydrogen evolution reaction, while nanopores can
promote NO<sub>3</sub><sup>–</sup> accumulation on the internal
surface of nanopores and confine the reaction intermediates within
the nanopores for a deeper NO<sub>3</sub><sup>–</sup> electroreduction.