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Chemolithotrophs are microorganisms that obtain energy by oxidizing inorganic molecules such as hydrogen gas (H₂), ammonia (NH₃), reduced sulfur compounds (H₂S, S²⁻), and ferrous iron (Fe²⁺). Unlike heterotrophic organisms that rely on organic carbon, chemolithotrophs transfer electrons from these inorganic donors to the electron transport chain (ETC), generating a proton motive force (PMF) that drives ATP synthesis through oxidative phosphorylation.
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Ladder diagrams are useful tools for understanding redox equilibrium reactions, especially the effects of concentration changes on the electrochemical potential of the reaction. The vertical axis in the redox ladder diagrams represents the electrochemical potential, E. The area of predominance is demarcated using the Nernst equation.
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Electrodeposition is a technique used to separate an analyte from interferents by electrochemical processes. Here, the analyte is a metal ion that can be deposited on an electrode immersed in the sample solution. The electrochemical setup consists of an anode and a cathode. When an electric current is applied to the setup, oxidation occurs at the anode. At the cathode, which consists of a large metal surface, metal ions undergo reduction and deposit onto the surface.
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Updated: Sep 12, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
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pH-Dependent Electroreduction of Nitrate on Fe Single-Atom Catalyst.

Zhen Meng1, Adyasa Priyadarsini2, Kaige Shi3

  • 1Department of Chemistry, University of Central Florida, Orlando, Florida, 32816, US.

Chemsuschem
|August 7, 2025
PubMed
Summary

Fe-N-C single-atom catalysts efficiently convert nitrate to ammonia across various pH levels. This study reveals the NHO*-mediated pathway and pH-dependent mechanisms, guiding the design of versatile nitrate reduction electrocatalysts.

Keywords:
Fe−N−Cammonia synthesiselectrocatalysisnitrate electroreductionselectivity

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Area of Science:

  • Electrochemistry
  • Materials Science
  • Catalysis

Background:

  • Electrochemical nitrate reduction reaction (NO3RR) is crucial for wastewater denitrification and ammonia (NH3) synthesis.
  • Fe-N-C single-atom catalysts offer well-defined active sites and stability for NO3RR.
  • Understanding pH dependence is key to optimizing catalyst performance.

Purpose of the Study:

  • Investigate the pH dependence of NO3RR on Fe-N-C catalysts.
  • Elucidate the reaction mechanism and selectivity origins.
  • Guide the development of broad pH-range electrocatalysts.

Main Methods:

  • Experimental electrochemical studies.
  • Density Functional Theory (DFT) calculations.
  • Analysis of Faradaic efficiency and reaction pathways.

Main Results:

  • Fe-N-C catalysts show high activity and >80% NH3 selectivity across acidic, neutral, and alkaline conditions.
  • Hydrogen evolution reaction (HER) competes most strongly in alkaline media.
  • DFT identified NHO*-mediated pathway as dominant for NO3RR and revealed pH-dependent potential-determining steps.

Conclusions:

  • Fe-N-C catalysts are effective for broad pH nitrate reduction.
  • Mechanistic insights explain pH-dependent selectivity.
  • This work provides a foundation for designing efficient, versatile nitrate recycling electrocatalysts.