All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

A survey of Earth-abundant metal oxides as oxygen evolution electrocatalysts in acidic media (pH < 1)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F23%3A10477106" target="_blank" >RIV/00216208:11320/23:10477106 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=5M5oMxvHNN" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=5M5oMxvHNN</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/D3EY00101F" target="_blank" >10.1039/D3EY00101F</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A survey of Earth-abundant metal oxides as oxygen evolution electrocatalysts in acidic media (pH < 1)

  • Original language description

    Electrolytic hydrogen appears as one of the most promising options to store renewable energy. In this water splitting process, the sluggish kinetics of the 4-electron oxygen evolution reaction (OER) with its high overpotentials have been widely regarded as the bottleneck to facilitate a fast, energy-efficient process. In alkaline media, numerous earth-abundant metal oxides are efficient OER catalysts, stabilized by the high concentration of hydroxide anions in the electrolyte. However, under acidic conditions, where the hydrogen evolution reaction (HER) is technologically preferred, only noble metal-based oxides (RuO2 and IrO2) are suitable OER catalysts, putting into question the scalability to wide-spread applications due to their scarcity and high cost. Most earth abundant metal oxides dissolve at high proton concentrations. A promising strategy to avoid this drawback consists of incorporating these catalysts into partially hydrophobic composite electrodes. Following this strategy, we have been able to conduct an extensive survey of the activity and stability of mono-, bi- and trimetallic earth-abundant transition metal oxides during the electrocatalytic OER under strongly acidic conditions. Our results confirm the general validity of the strategy by using a hydrophobic electrode to confer high stability to common metal oxides under these harsh conditions. Among all OER catalysts investigated, we found that simple manganese oxides appeared as the most active also exhibiting high, long-term stability. In particular, the stability of Mn2O3 oxide in the OER in acidic media was well confirmed by post-electrolysis characterization data.

  • 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

    10305 - Fluids and plasma physics (including surface physics)

Result continuities

  • Project

    <a href="/en/project/GN22-18079O" target="_blank" >GN22-18079O: POLAR-PEC: Unveiling the (photo/electro) catalytic properties of polar metal oxide surfaces</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EES Catalysis

  • ISSN

    2753-801X

  • e-ISSN

    2753-801X

  • Volume of the periodical

    1

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    765-773

  • UT code for WoS article

    001363337100001

  • EID of the result in the Scopus database

    2-s2.0-85189979654