Uniting Synergistic Effect of Single‐Ni Site and Electric Field of B‐ Bridged‐N for Boosted Electrocatalytic Nitrate Reduction to Ammonia

Author:

Ajmal Saira1,Kumar Anuj2,Mushtaq Muhammad Asim1,Tabish Mohammad3,Zhao Yulin4,Zhang Wenbin1,Khan Abdul Sammed1,Saad Ali5,Yasin Ghulam1ORCID,Zhao Wei1ORCID

Affiliation:

1. Institute for Advanced Study Shenzhen University Shenzhen Guangdong 518060 China

2. Nano‐Technology Research Laboratory Department of Chemistry GLA University Mathura Uttar Pradesh 281406 India

3. College of Materials Science and Engineering Beijing University of Chemical Technology Beijing 100029 China

4. School of Materials and Chemistry Southwest University of Science and Technology Mianyang 621010 China

5. Centre for Water Technology (WATEC) & Department of Biological and Chemical Engineering Aarhus University Universitetsbyen 36 Aarhus C 8000 Denmark

Abstract

AbstractElectrochemical conversion of nitrate, a prevalent water pollutant, to ammonia (NH3) is a delocalized and green path for NH3 production. Despite the existence of different nitrate reduction pathways, selectively directing the reaction pathway on the road to NH3 is now hindered by the absence of efficient catalysts. Single‐atom catalysts (SACs) are extensively investigated in a wide range of catalytic processes. However, their application in electrocatalytic nitrate reduction reaction (NO3RR) to NH3 is infrequent, mostly due to their pronounced inclination toward hydrogen evolution reaction (HER). Here, Ni single atoms on the electrochemically active carrier boron, nitrogen doped‐graphene (BNG) matrix to modulate the atomic coordination structure through a boron‐spanning strategy to enhance the performance of NO3RR is designed. Density functional theory (DFT) study proposes that BNG supports with ionic characteristics, offer a surplus electric field effect as compared to N‐doped graphene, which can ease the nitrate adsorption. Consistent with the theoretical studies, the as‐obtained NiSA@BNG shows higher catalytic activity with a maximal NH3 yield rate of 168 µg h−1 cm−2 along with Faradaic efficiency of 95% and promising electrochemical stability. This study reveals novel ways to rationally fabricate SACs' atomic coordination structure with tunable electronic properties to enhance electrocatalytic performance.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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