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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Efficient Electrochemical N2 Fixation over Donor-Acceptor FeEu─N4 Active Site
Zhiya Han1, Shiyu Zhang1, Yiting Xu2
1School of Materials, Shanghai Dianji University, No.300, Shuihua Road, Pudong New Area, Shanghai, 200245, China.
Abstract:
Electrocatalytic nitrogen reduction reaction (NRR) represents a promising approach to sustainable ammonia production, but the low Faradaic efficiency (FE) and poor ammonia yield rate limit its practical application. This work demonstrates an innovative FeEu─NC catalyst that leverages distinct donor-acceptor electron pairs between Fe and Eu atoms to significantly enhance the electrocatalytic NRR. The FeEu─NC catalyst demonstrates an outstanding ammonia yield of 221.6 µg h-1 mgcat -1 and a Faradaic efficiency of 61.1%, surpassing most previously reported NRR catalysts. Comprehensive experimental characterization indicates that electron transfer from Eu to Fe atoms weakens the N≡N bond, enhances N2 activation, and reduces the energy barrier of the potential-determining step, compared to Fe─NC. Furthermore, the difference in limiting potentials between the hydrogen evolution reaction (HER) and NRR suggests that the FeEu─NC catalyst prioritizes NRR over HER, enhancing its efficiency for ammonia synthesis. This work provides a blueprint for constructing highly active and selective electrocatalysts by exploiting intermetallic electron transfer, offering significant insights into the design of efficient electrochemical nitrogen fixation systems.
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