Articles producció científica> Química Física i Inorgànica

Molecular TiO2 Modifications of Supported PPh3-Capped Pd Nanocatalysts for CO2 Hydrogenation into Formates

  • Identification data

    Identifier: imarina:9380050
    Authors:
    Fernandez-Martinez, Maria DoloresGodard, Cyril
    Abstract:
    TiO2-supported Pd NPs-based materials were prepared following two distinct approaches: For the first set of materials 1-8, modification of the TiO2 support was performed prior to Pd NPs deposition, while the second set (9-15) was synthesized by deposition of modifiers over pre-synthesized Pd-PPh3/TiO2. These catalysts were applied in the hydrogenation of CO2 to formate, and their performance was compared with that of the unmodified Pd-PPh3/TiO2. Modification of the TiO2 support by organosilanes provided a beneficial effect in catalysis compared with the catalyst containing unmodified TiO2 or TiO2 modified by organophosphonic acids. In contrast, in most cases, the deposition of modifiers over previously synthesized Pd NPs supported on TiO2 was not beneficial to the activity of the catalyst. Interestingly, upon recycling, the first set of catalysts suffered a rapid decrease in activity, while the anchoring of modifiers over previously formed Pd NPs showed an improved stability (TON > 500 after the third recycling).
  • Others:

    Author, as appears in the article.: Fernandez-Martinez, Maria Dolores; Godard, Cyril
    Department: Química Física i Inorgànica
    URV's Author/s: Godard, Cyril
    Keywords: Amine groups At-silp Carbon-dioxide Catalyst modification Co2 hydrogenation Efficient synthesis Heterogeneous catalyst Ionic liquids Mesoporous silica Nanoparticle-silp catalysts Nanoparticles Palladium Palladium nanoparticles Surfac
    Abstract: TiO2-supported Pd NPs-based materials were prepared following two distinct approaches: For the first set of materials 1-8, modification of the TiO2 support was performed prior to Pd NPs deposition, while the second set (9-15) was synthesized by deposition of modifiers over pre-synthesized Pd-PPh3/TiO2. These catalysts were applied in the hydrogenation of CO2 to formate, and their performance was compared with that of the unmodified Pd-PPh3/TiO2. Modification of the TiO2 support by organosilanes provided a beneficial effect in catalysis compared with the catalyst containing unmodified TiO2 or TiO2 modified by organophosphonic acids. In contrast, in most cases, the deposition of modifiers over previously synthesized Pd NPs supported on TiO2 was not beneficial to the activity of the catalyst. Interestingly, upon recycling, the first set of catalysts suffered a rapid decrease in activity, while the anchoring of modifiers over previously formed Pd NPs showed an improved stability (TON > 500 after the third recycling).
    Thematic Areas: Astronomia / física Catalysis Chemistry, physical Ciências biológicas ii Engenharias ii Environmental science (all) Farmacia Physical and theoretical chemistry Química
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    Author's mail: cyril.godard@urv.cat
    Author identifier: 0000-0001-5762-4904
    Record's date: 2024-09-21
    Papper version: info:eu-repo/semantics/publishedVersion
    Papper original source: Catalysts. 14 (8): 487-
    APA: Fernandez-Martinez, Maria Dolores; Godard, Cyril (2024). Molecular TiO2 Modifications of Supported PPh3-Capped Pd Nanocatalysts for CO2 Hydrogenation into Formates. Catalysts, 14(8), 487-. DOI: 10.3390/catal14080487
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2024
    Publication Type: Journal Publications
  • Keywords:

    Catalysis,Chemistry, Physical,Physical and Theoretical Chemistry
    Amine groups
    At-silp
    Carbon-dioxide
    Catalyst modification
    Co2 hydrogenation
    Efficient synthesis
    Heterogeneous catalyst
    Ionic liquids
    Mesoporous silica
    Nanoparticle-silp catalysts
    Nanoparticles
    Palladium
    Palladium nanoparticles
    Surfac
    Astronomia / física
    Catalysis
    Chemistry, physical
    Ciências biológicas ii
    Engenharias ii
    Environmental science (all)
    Farmacia
    Physical and theoretical chemistry
    Química
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