Metal-Nitrogen-Carbon Catalysts for Electrochemical CO₂ Reduction: From Design to Industrial Applications

Abstract

Electrochemical CO₂ reduction reaction (eCO₂RR) offers a promising route for converting CO₂ into value-added chemicals and fuels using renewable electricity. Developing efficient, stable, and scalable catalysts is key to advancing this technology for commercialization. As non-precious metal catalysts, transition metal-nitrogen-doped carbon (M-N-C) materials have demonstrated excellent catalytic performance due to their tunable electronic structure, high activity, and structural stability. Herein, we provide a comprehensive overview of our group’s work in designing and optimizing M-N-C catalysts for eCO₂RR, focusing on metal site engineering, carbon substrate modification, and heteroatom doping strategies to enhance electrocatalytic efficiency and selectivity. We have also discussed the challenges and progresses in scaling up M-N-C catalysts synthesis, integrating M-N-C materials into membrane electrode assembly (MEA) electrolyzers, and employing tandem electrocatalytic systems to achieve multi-carbon products. Comparisons between tandem catalysts and tandem electrolyzers based on M-N-C materials are presented. The potential of coupling eCO₂RR with thermocatalysis for producing other high-value products is also briefly discussed. We envision that M-N-C catalysts based eCO₂RR will offer a viable pathway for cost-effective CO₂ utilization, while future research may focus on demonstrating long-term stability in large-scale electrolyzers and development of efficient tandem reactor systems to further validate the commercialization potential.

Article information

Article type
Feature Article
Submitted
24 apr 2025
Accepted
09 jun 2025
First published
12 jun 2025
This article is Open Access
Creative Commons BY license

Chem. Commun., 2025, Accepted Manuscript

Metal-Nitrogen-Carbon Catalysts for Electrochemical CO₂ Reduction: From Design to Industrial Applications

S. Wang, A. Badreldin and Y. Li, Chem. Commun., 2025, Accepted Manuscript , DOI: 10.1039/D5CC02297E

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