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Electrocatalytic activity of layered MAX phases for the hydrogen evolution reaction

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62156489%3A43210%2F21%3A43919665" target="_blank" >RIV/62156489:43210/21:43919665 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216305:26620/21:PU140737

  • Result on the web

    <a href="https://doi.org/10.1016/j.elecom.2021.106977" target="_blank" >https://doi.org/10.1016/j.elecom.2021.106977</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.elecom.2021.106977" target="_blank" >10.1016/j.elecom.2021.106977</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Electrocatalytic activity of layered MAX phases for the hydrogen evolution reaction

  • Original language description

    The hydrogen evolution reaction (HER) is important for the advancement of next-generation electrochemical energy devices. The search for an alternative inexpensive catalyst for energy conversion to replace expensive and rare noble metals is of high priority. There has been a significant push to investigate electrocatalysis of various layered materials for hydrogen evolution. However, the electrocatalytic activity of layered MAX phases remains largely unexplored. Herein, electrocatalytic activity studies of MAX (Ti2AlC, Ta2AlC, Ti2SnC, Ti3SiC2, V2AlC, Mo2TiAlC2, and Cr2AlC) phases are conducted. Material and electrochemical characterization are carried out to understand the morphology and catalytic activity, respectively. From Tafel slope analysis, it was found that proton adsorption is the rate-limiting step for all the MAX phases studied. Double transition-metal MAX carbides (Mo2TiAlC2) showed better catalytic activity for HER than single transition-metal MAX carbides.

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Electrochemistry Communications

  • ISSN

    1388-2481

  • e-ISSN

  • Volume of the periodical

    125

  • Issue of the periodical within the volume

    April

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    4

  • Pages from-to

    106977

  • UT code for WoS article

    000641414900002

  • EID of the result in the Scopus database

    2-s2.0-85102778248