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Unveiling binder-free hierarchically interlinked MoS2 nanosheet integrated Co9S8 nanosheet in a nanohybrid architecture framework coupled with in-situ anion exchange engineering from its corresponding oxygen counterparts for advanced supercapacitor

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23640%2F25%3A43976030" target="_blank" >RIV/49777513:23640/25:43976030 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.jallcom.2025.182283" target="_blank" >https://doi.org/10.1016/j.jallcom.2025.182283</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jallcom.2025.182283" target="_blank" >10.1016/j.jallcom.2025.182283</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Unveiling binder-free hierarchically interlinked MoS2 nanosheet integrated Co9S8 nanosheet in a nanohybrid architecture framework coupled with in-situ anion exchange engineering from its corresponding oxygen counterparts for advanced supercapacitor

  • Original language description

    Engineering hybrid nanoarchitecture materials, which feature meticulously designed hierarchical frameworks and components, represents a highly effective approach to meeting the demanding performance requirements of supercapacitors (SCs). Herein, we present a simple and affordable anion exchange strategy to tailor a unique, multifaceted transition metal chalcogenide of MoS2 integrated with Co9S8 (CMS) nanohybrid hierarchical framework grown on a porous Ni-foam substrate, serving as a free-standing electrode for SC. It examines the effect of anion exchange processes on electrochemical performance, demonstrating significant enhancements in various metrics. The CMS nanohybrid material exhibits a hierarchical architecture along with outstanding intrinsic conductivity, which collectively enhances its electrochemical performance and ion/charge transfer efficiency. This improvement is attributed to the synergistic effects of the component, which facilitate more efficient electrochemical reactions and mitigate the volume expansion associated with charging and discharging. Interestingly, the CMS nanohybrid electrode exhibits an impressive specific capacitance of ∼1325 F g−1 at a current density of 1 A g−1, along with a substantial rate capability of ∼63.6 % at 20 A/g, significantly surpassing those of their hybrid metal oxide counterparts. Additionally, the hybrid supercapacitor comprising CMS and activated carbon achieved a specific capacitance of ∼246 F g−1 at a current density of 1 A g−1, a maximum energy density of ∼76.73 Wh kg−1, and a power density of ∼19.06 kW kg−1, while maintaining ∼91.7 % cycling stability after 12,000 cycles. Thus, this work could provide a framework for integrating advanced bimetallic chalcogenides to enhance energy storage performance.

  • 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

    JOURNAL OF ALLOYS AND COMPOUNDS

  • ISSN

    0925-8388

  • e-ISSN

    1873-4669

  • Volume of the periodical

    1037

  • Issue of the periodical within the volume

    AUG 10 2025

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    13

  • Pages from-to

    nestránkováno

  • UT code for WoS article

    001541218100001

  • EID of the result in the Scopus database

    2-s2.0-105010558822