Počet záznamů: 1
Cyclohexane Oxidative Dehydrogenation on Graphene-Oxide-Supported Cobalt Ferrite Nanohybrids: Effect of Dynamic Nature of Active Sites on Reaction Selectivity
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SYSNO ASEP 0577175 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Cyclohexane Oxidative Dehydrogenation on Graphene-Oxide-Supported Cobalt Ferrite Nanohybrids: Effect of Dynamic Nature of Active Sites on Reaction Selectivity Tvůrce(i) Kadam, Shashikant Arun (UFCH-W)
Sandoval, S. (ES)
Bastl, Zdeněk (UFCH-W) RID, ORCID
Simkovičová, Karolína (UFCH-W) ORCID
Kvítek, L. (CZ)
Jašík, Juraj (UFCH-W) ORCID, RID
Olszówka, Joanna Elżbieta (UFCH-W) ORCID
Valtera, Stanislav (UFCH-W) ORCID, RID
Vaidulych, Mykhailo (UFCH-W) ORCID, RID
Morávková, Jaroslava (UFCH-W) RID, ORCID
Sazama, Petr (UFCH-W) RID, ORCID
Kubička, D. (CZ)
Travert, A. (FR)
van Bokhoven, J. A. (CH)
Fortunelli, A. (IT)
Kleibert, A. (CH)
Kalbáč, Martin (UFCH-W) RID, ORCID
Vajda, Štefan (UFCH-W) RID, ORCIDZdroj.dok. ACS Catalysis. - : American Chemical Society - ISSN 2155-5435
Roč. 13, č. 20 (2023), s. 13484-13505Poč.str. 22 s. Jazyk dok. eng - angličtina Země vyd. US - Spojené státy americké Klíč. slova spinel ; CoFe2O4 ; rgo ; cyclohexane ; oxidativedehydrogenation ; xpeem ; support effects in catalysis ; dynamic active sites Vědní obor RIV CF - Fyzikální chemie a teoretická chemie Obor OECD Physical chemistry CEP 8J22FR025 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy EF16_013/0001821 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy LM2023066 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy GX20-08633X GA ČR - Grantová agentura ČR Způsob publikování Open access Institucionální podpora UFCH-W - RVO:61388955 UT WOS 001079423700001 EID SCOPUS 85176120698 DOI https://doi.org/10.1021/acscatal.3c02592 Anotace In this work, we investigated cyclohexane oxidative dehydrogenation (ODH) catalyzed by cobalt ferrite nanoparticles supported on reduced graphene oxide (RGO). We aim to identify the active sites that are specifically responsible for full and partial dehydrogenation using advanced spectroscopic techniques such as X-ray photoelectron emission microscopy (XPEEM) and X-ray photoelectron spectroscopy (XPS) along with kinetic analysis. Spectroscopically, we propose that Fe3+/T(d )sites could exclusively produce benzene through full cyclohexane dehydrogenation, while kinetic analysis shows that oxygen-derived species (O*) are responsible for partial dehydrogenation to form cyclohexene in a single catalytic sojourn. We unravel the dynamic cooperativity between octahedral and tetrahedral sites and the unique role of the support in masking undesired active (Fe3+/T-d) sites. This phenomenon was strategically used to control the abundance of these species on the catalyst surface by varying the particle size and the wt % content of the nanoparticles on the RGO support in order to control the reaction selectivity without compromising reaction rates which are otherwise extremely challenging due to the much favorable thermodynamics for complete dehydrogenation and complete combustion under oxidative conditions. Pracoviště Ústav fyzikální chemie J.Heyrovského Kontakt Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Rok sběru 2024 Elektronická adresa https://hdl.handle.net/11104/0346399
Počet záznamů: 1