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Regulating protonation paths for enhanced photocatalytic CO2 methanation by coupling Pt sites on WO2.9/TiO2

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15640%2F25%3A73631169" target="_blank" >RIV/61989592:15640/25:73631169 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2025/cy/d5cy00167f" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2025/cy/d5cy00167f</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d5cy00167f" target="_blank" >10.1039/d5cy00167f</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Regulating protonation paths for enhanced photocatalytic CO2 methanation by coupling Pt sites on WO2.9/TiO2

  • Original language description

    CO2 methanation via photocatalysis with water vapor is a sustainable technique for reducing CO2 emission but is challenged by the high energy barrier associated with the initial adsorption, activation and protonation of CO2 molecules. In this work, a substoichiometric WO2.9 thin film with strong Lewis acidity was coated on TiO2 microspheres, followed by the deposition of Pt cocatalysts on WO2.9 with controlled Pt single atoms and clusters (Pt-WO2.9/TiO2). The methane production rate reached 10.74 mu mol h-1 g-1 with a selectivity of 99.8%, which was similar to 40 times higher than that of bare TiO2 (0.27 mu mol h-1 g-1). The high methane production rate was attributed to the synergy of Pt sites on the WO2.9/TiO2 heterojunction, where the Pt clusters facilitated water dissociation, thereby providing H* through hydrogen spillover on the surface, and the presence of a substoichiometric WO2.9 surface further enhanced the spillover process. The high density of active H* promoted the protonation pathway for CO2 activation (CO2 -&gt; COOH+ -&gt; *COOH), which improved the adsorption of the essential intermediate *CO on Pt single atoms and displayed a significantly reduced energy barrier for the protonation reaction of C1 intermediates, resulting in a mixed reaction pathway. This work provides new insights into a mechanism to regulate the reaction path to facilitate efficient photocatalytic CO2 methanation.

  • 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

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Catalysis Science &amp; Technology

  • ISSN

    2044-4753

  • e-ISSN

    2044-4761

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    13

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    4002-4011

  • UT code for WoS article

    001501454100001

  • EID of the result in the Scopus database

    2-s2.0-105007861479