Boosting Cobalt Porphyrin for Selective Nitrate Electroreduction

B Bulin Chen (State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China) J Jie Zao (State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China) Y Yirong Tang (State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China) X Xichen Zhou (Department of Chemistry) W Wentao Zhang P Peiyi Han (State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China) Y Yongye Liang (Southern University of Science and Technology , , ,) Z Zhan Jiang (State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China)

Abstract

ABSTRACT The electrocatalytic reduction of nitrate (NO 3 − ) to ammonia (NH 3 ) offers a sustainable pathway for NH 3 synthesis. Metal porphyrins are promising electrocatalysts for the NO 3 − reduction reactions (NO 3 RR) due to their tunable molecular structures, yet effective strategies for enhancing their performance are still lacking. Herein, we develop an efficient composite electrocatalyst based on cobalt tetraphenylporphyrin (CoTPP) for electrochemical NH 3 synthesis by mitigating hydroxide (OH − ) interference and optimizing active hydrogen supply. CoTPP is identified as a superior catalyst with a strong affinity for NO 3 − adsorption, and neutral condition is adopted to suppress the competitive OH − adsorption. Poly(benzodifurandione) (PBFDO) is further introduced as an active hydrogen support cocatalyst. The optimized composite catalyst of CoTPP+carbon nanotube (CNT)+PBFDO shows high Faradaic efficiencies (FEs) of NH 3 near 100% across a broad potential range, and a high NH 3 yield rate (5.3 mg h −1 cm −2 ) is achieved, increasing by fivefold when compared to the catalyst without PBFDO. This work provides mechanistic insights into enhancing the activity of molecular electrocatalysts for the conversion of NO 3 − to NH 3 .

Article Details

Volume / Issue Vol. 65, Issue 25
Published June 15, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

B

Bulin Chen

State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China

J

Jie Zao

State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China

Y

Yirong Tang

State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China

X

Xichen Zhou

Department of Chemistry

W

Wentao Zhang

P

Peiyi Han

State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China

Y

Yongye Liang

Southern University of Science and Technology , , ,

Z

Zhan Jiang

State Key Laboratory of Quantum Functional Materials Shenzhen Key Laboratory of Printed Organic Electronics Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China