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dc.contributor.authorPetallidou, Klito C.en
dc.contributor.authorKalamaras, Christos M.en
dc.contributor.authorEfstathiou, Angelos M.en
dc.creatorPetallidou, Klito C.en
dc.creatorKalamaras, Christos M.en
dc.creatorEfstathiou, Angelos M.en
dc.date.accessioned2019-11-21T06:22:14Z
dc.date.available2019-11-21T06:22:14Z
dc.date.issued2014
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/56008
dc.description.abstractPlatinum nanoparticles supported on single CeO2 and TiO 2 metal oxides and Ce0.8Ti0.2O 2-δ solid solution were prepared to investigate the effect of Ti4+-doping of ceria on important mechanistic and kinetic aspects of the Water-Gas Shift (WGS) reaction in the 200-300 °C range, namely: (i) the concentration and chemical structure of active adsorbed reaction intermediates present in the C-path and H-path of WGS, and (ii) the prevailing mechanistic path among "redox" and "associative" both proposed in the literature. The relationship between the chemical nature of dopant (Zr 4+, Ti4+ and La3+) and the concentration of active C-pool and H-pool of reaction intermediates as well as that of specific rate per gram basis (rCO, μmol g-1 s-1) for the ceria-doped supported Pt is illustrated for the first time based on relevant results previously reported (Zr4+ and La3+-doped ceria). The 0.5 wt% Pt supported on Ce0.8Ti0.2O 2-δ (Ti4+-doped CeO2) exhibits significantly higher WGS activity in terms of CO conversion (%) and specific kinetic rate (μmol CO g-1 s-1 or μmol CO cm -1 s-1) compared to Pt/CeO2, Pt/TiO 2, Pt/Ce0.8La0.2O2-δ and Pt/Ce0.5Zr0.5O2-δ catalysts. This was explained mainly by: (i) the larger concentration of active C-pool of reaction intermediates formed around each Pt nanoparticle, and (ii) the higher reactivity of sites (k, s-1) along the Pt-support interface responsible for CO2 and H2 formation. A very good correlation between the concentration of active C-pool and the specific reaction rate, rCO (μmol g-1 s-1) as a function of the dopant (Zr 4+, La3+ and Ti4+) was found. The concentration of labile surface oxygen and its mobility in Ce0.8Ti 0.2O2-δ compared to CeO2 (undoped), La3+ or Zr4+-doped ceria are also important factors. It is proposed that on Pt/CeO2-doped catalysts the WGS reaction follows both the "redox" and "associative formate" mechanisms, where the extent of participation of each mechanism depends on the chemical nature of the dopant (Zr4+, La3+ and Ti4+). © 2013 Elsevier B.V. All rights reserved.en
dc.sourceCatalysis Todayen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84896920519&doi=10.1016%2fj.cattod.2013.10.081&partnerID=40&md5=c909ef3569ab658a42b867d6ebcf0ac3
dc.subjectCarbon dioxideen
dc.subjectPlatinumen
dc.subjectLakesen
dc.subjectDoping (additives)en
dc.subjectNanoparticlesen
dc.subjectTitaniumen
dc.subjectCatalystsen
dc.subjectZirconiumen
dc.subjectOperandoen
dc.subjectWater gas shiften
dc.subjectWGS reactionsen
dc.subjectReaction intermediatesen
dc.subjectSSITKA-DRIFTSen
dc.subjectSSITKA-MSen
dc.subjectSupported Pten
dc.subjectWGS reaction mechanismen
dc.subjectOperando studiesen
dc.subjectCeria-doped supported Pten
dc.subjectTransient isotopic techniquesen
dc.titleThe effect of La3+, Ti4+ and Zr4+ dopants on the mechanism of WGS on ceria-doped supported Pt catalystsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.cattod.2013.10.081
dc.description.volume228
dc.description.startingpage183
dc.description.endingpage193
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :16</p>en
dc.source.abbreviationCatal Todayen
dc.contributor.orcidEfstathiou, Angelos M. [0000-0001-8393-8800]
dc.contributor.orcidKalamaras, Christos M. [0000-0001-6809-5948]
dc.gnosis.orcid0000-0001-8393-8800
dc.gnosis.orcid0000-0001-6809-5948


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