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All-Electrochem-Active Graphite Electrode Enabled by Manipulating Li+ Activity of Inactive Components for High-Energy Batteries

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27640%2F25%3A10258333" target="_blank" >RIV/61989100:27640/25:10258333 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.acs.org/doi/10.1021/acsaem.5c00794" target="_blank" >https://pubs.acs.org/doi/10.1021/acsaem.5c00794</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acsaem.5c00794" target="_blank" >10.1021/acsaem.5c00794</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    All-Electrochem-Active Graphite Electrode Enabled by Manipulating Li+ Activity of Inactive Components for High-Energy Batteries

  • Original language description

    Graphite anodes have approached their theoretical specific capacity of 372 mA h g–1, which becomes an obstacle for further increasing the energy density of commercial lithium-ion batteries. Various strategies have been proposed to enhance the energy density of graphite-based full batteries, such as decreasing the usage of inactive binders and conductive additives and exploring graphite/SiOx composite anodes. Nevertheless, the anodes cannot balance energy density, power density, and cycling stability. In this study, we designed an all-electrochem-active graphite electrode by manipulating the Li+ activity of the inactive components to improve the energy density of the entire electrode. In our study, colloidal two-dimensional titanium carbide nanosheets (MXene) were employed as binders, and carbon-coated titanium dioxide nanoparticles with oxygen defects (TiO2–x@C) acted as conductive additives in the electrode configurations. Both MXene and TiO2–x@C can function as active materials to store lithium ions by reversible insertion and extraction with little electrochemical degradation. As a result, the all-electrochem-active graphite electrodes demonstrated a superior specific capacity of 394 mA h g–1 at a current density of 0.2C after 300 cycles. This concept of all-electrochem-active electrodes is anticipated to inspire future research on high-energy-density batteries by activating the Li+ affinities of binders and conductive additives.

  • 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

    21000 - Nano-technology

Result continuities

  • Project

  • Continuities

    O - Projekt operacniho programu

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

    ACS Applied Energy Materials

  • ISSN

    2574-0962

  • e-ISSN

  • Volume of the periodical

    8

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    8277-8287

  • UT code for WoS article

    001506459000001

  • EID of the result in the Scopus database

    2-s2.0-105007880815