Atomic Co─P Catalytic Pair Drives Efficient Electrochemical Nitrate Reduction to Ammonia

Author:

Ni Jiaqi1,Yan Jing1,Li Fuhua2,Qi Haifeng3,Xu Qingzhu1,Su Chenliang1,Sun Like1,Sun Hongli1,Ding Jie2,Liu Bin24ORCID

Affiliation:

1. International Collaboration Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education Institute of Microscale Optoelectronics Shenzhen University Shenzhen 518060 China

2. Department of Materials Science and Engineering City University of Hong Kong Hong Kong SAR 999077 China

3. Department of Renewable Resources Leibniz‐Institute for Catalysis Albert Einstein Street 29a 18059 Rostock Germany

4. Department of Chemistry & Center of Super‐Diamond and Advanced Films (COSDAF) City University of Hong Kong Hong Kong SAR 999077 China

Abstract

AbstractElectrochemically reducing nitrate (NO3), a common water pollutant, to valuable ammonia (NH3) offers a green, sustainable, and decentralized route for ammonia synthesis. Electrochemical nitrate reduction reaction (NO3RR) involves two crucial reaction steps: nitrate deoxygenation followed by nitrite hydrogenation; in particular, the nitrite hydrogenation reaction is the rate‐determining step (RDS) for NO3RR. In this work, an atomically dispersed cobalt‐phosphorus (Co─P) catalytic pair (CP) with strong electronic coupling is reported. The Co site in Co─P CP effectively activates NO3, while the P site in Co─P CP facilitates water dissociation to release H+, synergistically enhancing the thermodynamic and kinetic performance of electrochemical nitrate reduction to ammonia.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Department of Education of Guangdong Province

China Postdoctoral Science Foundation

Publisher

Wiley

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