# Graphene Oxide-Anchored Cu–Co Catalysts for Efficient Electrochemical Nitrate Reduction

**Authors:** Haosheng Lan, Yi Zhang, Le Ding, Xin Li, Zhanhong Zhao, Yansen Qu, Yingjie Xia, Xinghua Chang

PMC · DOI: 10.3390/ma18112495 · Materials · 2025-05-26

## TL;DR

This paper presents a new bimetallic catalyst for efficiently converting nitrate to ammonia, offering environmental and industrial benefits.

## Contribution

The study introduces a Cu–Co bimetallic catalyst on graphene oxide with high selectivity and efficiency for nitrate reduction.

## Key findings

- Cu6Co4/RGO achieved 99.86% ammonia selectivity and 96.54% Faradaic efficiency at −0.6 V.
- The catalyst maintained over 90% efficiency for 20 hours, showing excellent durability.
- Co enhanced water dissociation, promoting hydrogen generation and nitrate transformation.

## Abstract

Electrocatalytic nitrate reduction to ammonia (ENRA) presents a promising strategy for simultaneous environmental remediation and sustainable ammonia synthesis. In this work, a Cu–Co bimetallic catalyst supported on functionalized reduced graphene oxide (RGO) was systematically designed to achieve efficient and selective ammonia production. Surface oxygen functional groups on graphene oxide (GO) were optimized through alkaline hydrothermal treatments, enhancing the anchoring capacity for metal active sites. Characterization indicated the successful formation of uniform Cu–Co bimetallic heterointerfaces comprising metallic and oxide phases, which significantly improved catalyst stability and performance. Among the studied compositions, Cu6Co4/RGO exhibited superior catalytic activity, achieving a remarkable ammonia selectivity of 99.86% and a Faradaic efficiency of 96.54% at −0.6 V (vs. RHE). Long-term electrocatalysis demonstrated excellent durability, with over 90% Faradaic efficiency maintained for ammonia production after 20 h of operation. In situ FTIR analysis revealed that introducing Co effectively promoted water dissociation, facilitating hydrogen generation (*H) and accelerating the transformation of nitrate intermediates. This work offers valuable mechanistic insights and paves the way for the design of highly efficient bimetallic electrocatalysts for nitrate reduction and ammonia electrosynthesis.

## Linked entities

- **Chemicals:** ammonia (PubChem CID 222), nitrate (PubChem CID 943)

## Full-text entities

- **Chemicals:** H (MESH:D006859), GO (MESH:C000628730), ammonia (MESH:D000641), Cu-Co (-), water (MESH:D014867), oxygen (MESH:D010100), Co (MESH:D003035), oxide (MESH:D010087), Nitrate (MESH:D009566), Cu (MESH:D003300)

## Full text

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## Figures

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## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12156831/full.md

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Source: https://tomesphere.com/paper/PMC12156831