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Peroxide-Driven Nitrogen Fixation Reactions for Energy Storage Applications

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23640%2F25%3A43976439" target="_blank" >RIV/49777513:23640/25:43976439 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/aenm.202501583" target="_blank" >https://doi.org/10.1002/aenm.202501583</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/aenm.202501583" target="_blank" >10.1002/aenm.202501583</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Peroxide-Driven Nitrogen Fixation Reactions for Energy Storage Applications

  • Original language description

    Electrochemical nitrogen fixation offers a sustainable and environmentally friendly alternative to conventional ammonia synthesis, yet it currently faces significant challenges in terms of energy efficiency, catalytic activity, and economic feasibility. Here, this work presents a novel peroxide-mediated dual-step strategy designed to efficiently address these challenges using advanced energy materials. Ruthenium oxide and cobalt phthalocyanine catalysts facilitate simultaneous hydrogen peroxide formation and nitrogen oxidation to nitrate (NO3-$rm{NO}_{3}&lt;^&gt;{-}$) at an exceptionally low potential of 0.1 V versus RHE, achieving a nitrate yield of 71.1 +/- 4.2 mu g h-(1) cm-2 and a Faradaic efficiency (FE) of 2.1 +/- 0.4%. Subsequently, the in situ generated NO3-$rm{NO}_{3}&lt;^&gt;{-}$ is electrochemically reduced to ammonia (NH3) at -0.35 V, delivering an impressive NH3 yield of 147.2 +/- 13.7 mu g h-(1) cm-2 with 13.8 +/- 1.7% FE. This combined approach significantly outperforms traditional direct electrochemical nitrogen reduction methods, enhancing ammonia yield approximate to 30-fold. Furthermore, a detailed techno-economic analysis demonstrates substantial economic advantages, significantly reducing ammonia production costs compared to direct nitrogen reduction. Although this system remains somewhat more expensive than direct nitrate reduction, the latter faces inherent challenges such as limited substrate availability and preprocessing requirements. This work advances sustainable ammonia synthesis by introducing a highly effective catalytic strategy integrated with meaningful energy and economic considerations.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/EH22_008%2F0004572" target="_blank" >EH22_008/0004572: Quantum materials for applications in sustainable technologies</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Advanced Energy Materials

  • ISSN

    1614-6832

  • e-ISSN

    1614-6840

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    32

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    15

  • Pages from-to

    nestránkováno

  • UT code for WoS article

    001506206600001

  • EID of the result in the Scopus database

    2-s2.0-105007784017