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Nitrogen Fixation by Ru Single-Atom Electrocatalytic Reduction

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TLDR
In this paper, single Ru sites supported on N-doped porous carbon greatly promoted electroreduction of aqueous N2 selectively to NH3, affording an NH3 formation rate of 3.665 m g N H 3 h − 1 m g Ru − 1 at −0.21 V versus the reversible hydrogen electrode.
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This article is published in Chem.The article was published on 2019-01-10 and is currently open access. It has received 661 citations till now. The article focuses on the topics: Reversible hydrogen electrode & Overpotential.

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Non‐metal Single‐Iodine‐Atom Electrocatalysts for the Hydrogen Evolution Reaction

TL;DR: The SANi-I exhibits robust structural stability and exceptional electrocatalytic activity for the hydrogen evolution reaction, and in-situ Raman spectroscopy reveals that the hydrogen adatom is adsorbed by a single iodine atom, forming the I-Hads intermediate, which promotes the HER process.
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Recent progress in the electrochemical ammonia synthesis under ambient conditions

TL;DR: In this paper, a review of the electrocatalytic N2 reduction reaction (NRR) is presented, with a particular focus on the improvement of the catalytic activity and selectivity toward ammonia production through optimizing the electrolyte, pH and the structure of the catalyst.
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Mechanochemical Kilogram-Scale Synthesis of Noble Metal Single-Atom Catalysts

TL;DR: In this paper, a mechanochemical approach for the mass production of noble metal SACs was reported, and the successful formation of atomically dispersed palladium species on zinc oxide (Pd1/ZnO) was verified by aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption spectroscopy.
References
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Journal ArticleDOI

Efficient Visible Light Nitrogen Fixation with BiOBr Nanosheets of Oxygen Vacancies on the Exposed {001} Facets

TL;DR: It is demonstrated that efficient fixation of N2 to NH3 can proceed under room temperature and atmospheric pressure in water using visible light illuminated BiOBr nanosheets of oxygen vacancies in the absence of any organic scavengers and precious-metal cocatalysts.
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A theoretical evaluation of possible transition metal electro-catalysts for N2 reduction

TL;DR: Density functional theory calculations were used in combination with the computational standard hydrogen electrode to calculate the free energy profile for the reduction of N(2) admolecules and N adatoms on several close-packed and stepped transition metal surfaces in contact with an acidic electrolyte.
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Ammonia synthesis from first-principles calculations.

TL;DR: The rate of ammonia synthesis over a nanoparticle ruthenium catalyst can be calculated directly on the basis of a quantum chemical treatment of the problem using density functional theory, and offers hope for computer-based methods in the search for catalysts.
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Electrochemical Reduction of N2 under Ambient Conditions for Artificial N2 Fixation and Renewable Energy Storage Using N2/NH3 Cycle

TL;DR: Using tetrahexahedral gold nanorods as a heterogeneous electrocatalyst, an electrocatalytic N2 reduction reaction was shown to be possible at room temperature and atmospheric pressure, with a high Faradic efficiency up to 4.02% at -0.2 V vs reversible hydrogen electrode.
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The Challenge of Electrochemical Ammonia Synthesis: A New Perspective on the Role of Nitrogen Scaling Relations.

TL;DR: In this work, insights from DFT calculations that describe limitations on the low-temperature electrocatalytic production of NH3 from N2 are presented and new strategies for catalyst design are proposed that may help guide the search for an electrocatalyst that can achieve selective N2 reduction.
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