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High-entropy oxychloride increasing the stability of Li–sulfur batteries

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    SYSNO ASEP0572779
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHigh-entropy oxychloride increasing the stability of Li–sulfur batteries
    Author(s) Zukalová, Markéta (UFCH-W) RID, SAI, ORCID
    Fabián, M. (SK)
    Porodko, O. (SK)
    Vinarčíková, Monika (UFCH-W)
    Pitňa Lásková, Barbora (UFCH-W) ORCID
    Kavan, Ladislav (UFCH-W) RID, ORCID
    Source TitleRSC Advances. - : Royal Society of Chemistry
    Roč. 13, č. 25 (2023), s. 17008-17016
    Number of pages9 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsTiO2 ; Li-sulfur batteries ; electrocatalysis ; cathode ; separator
    Subject RIVCG - Electrochemistry
    OECD categoryPhysical chemistry
    R&D ProjectsGA20-03564S GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportUFCH-W - RVO:61388955
    UT WOS001002193600001
    EID SCOPUS85162815942
    DOI10.1039/D3RA01496G
    AnnotationA novel lithiated high-entropy oxychloride Li0.5(Zn0.25Mg0.25Co0.25Cu0.25)0.5Fe2O3.5Cl0.5 (LiHEOFeCl) with spinel structure belonging to the cubic Fd[3 with combining macron]m space group is synthesized by a mechanochemical–thermal route. Cyclic voltammetry measurement of the pristine LiHEOFeCl sample confirms its excellent electrochemical stability and the initial charge capacity of 648 mA h g−1. The reduction of LiHEOFeCl starts at ca. 1.5 V vs. Li+/Li, which is outside the electrochemical window of the Li–S batteries (1.7/2.9 V). The addition of the LiHEOFeCl material to the composite of carbon with sulfur results in improved long-term electrochemical cycling stability and increased charge capacity of this cathode material in Li–S batteries. The carbon/LiHEOFeCl/sulfur cathode provides a charge capacity of 530 mA h g−1 after 100 galvanostatic cycles, which represents ca. 33% increase as compared to the charge capacity of the blank carbon/sulfur composite cathode after 100 cycles. This considerable effect of the LiHEOFeCl material is assigned to its excellent structural and electrochemical stability within the potential window of 1.7 V/2.9 V vs. Li+/Li. In this potential region, our LiHEOFeCl has no inherent electrochemical activity. Hence, it acts solely as an electrocatalyst accelerating the redox reactions of polysulfides. This can be beneficial for the performance of Li–S batteries, as evidenced by reference experiments with TiO2 (P90).
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2024
    Electronic addresshttps://hdl.handle.net/11104/0343347
Number of the records: 1  

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