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Enhanced dual atomic Fe-Ni sites in N-doped carbon for bifunctional oxygen electrocatalysis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27710%2F22%3A10251028" target="_blank" >RIV/61989100:27710/22:10251028 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.webofscience.com/wos/woscc/full-record/WOS:000882774500004" target="_blank" >https://www.webofscience.com/wos/woscc/full-record/WOS:000882774500004</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.mtener.2022.101171" target="_blank" >10.1016/j.mtener.2022.101171</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Enhanced dual atomic Fe-Ni sites in N-doped carbon for bifunctional oxygen electrocatalysis

  • Original language description

    Atomically dispersed catalysts with high electrocatalytic performance are emerging as promising elec-trocatalysts for energy conversion and storage devices. Nevertheless, achieving superior bifunctional catalytic activity with single-atom catalysts toward reactions involving multi-intermediates is still facing great challenges. Herein, dual-atomic Fe-Ni pairs dispersed in hierarchical porous nitrogen-doped carbon (FeNi-HPNC) catalysts were successfully synthesized using a facile mechanochemical strategy. By virtue of the engineered electronic structure of Fe coordinated with Ni, the as-synthesized FeNi-HPNC with atomically dispersed dual-metal active sites and pore-rich structure exhibits remarkable bifunctional activities. A high half-wave potential of 0.868 V for oxygen reduction reaction and a low potential of 1.59 V at 10 mA/cm2 for oxygen evolution reaction have been obtained for FeNi-HPNC, which are superior to the single-atom catalysts of Fe-HPNC and Ni-HPNC, respectively, and are even greater than the precious metal catalysts. Combined experimental and theoretical results have revealed that the enhanced bifunctional catalytic activity of FeNi-HPNC is ascribed to the electronic interaction of Fe-Ni sites, which decreases the adsorption energy of oxygen intermediates during oxygen reduction reac-tion/oxygen evolution reaction. Furthermore, the practical application of FeNi-HPNC catalysts in Zn-air batteries has been demonstrated; a high peak power density and long-term durability are delivered.(c) 2022 Elsevier Ltd. All rights reserved.

  • 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

    20400 - Chemical engineering

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Materials Today Energy

  • ISSN

    2468-6069

  • e-ISSN

  • Volume of the periodical

    30

  • Issue of the periodical within the volume

    December 2022

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    nestrankovano

  • UT code for WoS article

    000882774500004

  • EID of the result in the Scopus database