Alloying of Cu with Ru Enabling the Relay Catalysis for Reduction of Nitrate to Ammonia

Author:

Gao Wensheng1ORCID,Xie Kefeng2,Xie Jin1,Wang Xiaomei1,Zhang Hong3,Chen Shengqi1,Wang Hao1,Li Zelong1,Li Can14ORCID

Affiliation:

1. Key Laboratory of Advanced Catalysis Gansu Province State Key Laboratory of Applied Organic Chemistry College of Chemistry and Chemical Engineering Lanzhou University Lanzhou Gansu 730000 China

2. School of Chemistry and Chemical Engineering Lanzhou Jiaotong University Lanzhou 730070 China

3. Electron Microscopy Centre of Lanzhou University School of Materials and Energy Lanzhou University Lanzhou Gansu 730000 China

4. State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian National Laboratory for Clean Energy Dalian Liaoning 116023 China

Abstract

AbstractInvolving eight electron transfer process and multiple intermediates of nitrate (NO3) reduction reaction leads to a sluggish kinetic and low Faradaic efficiency, therefore, it is essential to get an insight into the reaction mechanism to develop highly efficient electrocatalyst. Herein, a series of reduced‐graphene‐oxide‐supported RuCu alloy catalysts (RuxCux/rGO) are fabricated and used for the direct reduction of NO3 to NH3. It is found that the Ru1Cu10/rGO shows the ammonia formation rate of 0.38 mmol cm−2 h−1 (loading 1 mg cm−2) and the ammonia Faradaic efficiency of 98% under an ultralow potential of −0.05 V versus Reversible Hydrogen Electode (RHE), which is comparable to Ru catalyst. The highly efficient activity of Ru1Cu10/rGO can be attributed to the synergetic effect between Ru and Cu sites via a relay catalysis, in which the Cu shows the exclusively efficient activity for the reduction of NO3 to NO2 and Ru exhibits the superior activity for NO2 to NH3. In addition, the doping of Ru into Cu tunes the d‐band center of alloy and effectively modulates the adsorption energy of the NO3 and NO2, which promotes the direct reduction of NO3 to NH3. This synergetic electrocatalysis strategy opens a new avenue for developing highly efficient multifunctional catalysts.

Funder

Fundamental Research Funds for the Central Universities

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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