2004
DOI: 10.1016/j.jcat.2004.04.005
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Nature of the vanadia?ceria interface in V5+/CeO2 catalysts and its relevance for the solid-state reaction toward CeVO4 and catalytic properties

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Cited by 147 publications
(49 citation statements)
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“…This represents the first direct structure-spectroscopy relation for those materials, and disagrees with previous assumptions on those relations [20][21][22][23][24][25][26]. The photoelectron spectra recorded for the same set of preparations exhibits further interesting structure-property relations: The V2p spectra of the vanadia deposits reveal an oxidation state of V 5+ [27], compatible with a fourfold coordinated vanadyl containing species and indicating that the support is actively involved in determining the electronic structure through redox processes.…”
Section: Resultscontrasting
confidence: 86%
“…This represents the first direct structure-spectroscopy relation for those materials, and disagrees with previous assumptions on those relations [20][21][22][23][24][25][26]. The photoelectron spectra recorded for the same set of preparations exhibits further interesting structure-property relations: The V2p spectra of the vanadia deposits reveal an oxidation state of V 5+ [27], compatible with a fourfold coordinated vanadyl containing species and indicating that the support is actively involved in determining the electronic structure through redox processes.…”
Section: Resultscontrasting
confidence: 86%
“…The theoretical value for monolayer coverage of dehydrated VO x /TiO 2 catalysts is 7.9 atom/nm 2 [29]. Due to stronger interactions between vanadium and ceria, vanadium oxide species disperse on ceria up to 9 V atom/nm 2 of support determined by Raman Spectroscopy [31]. Vanadia reacts with cerium oxide to form CeVO 4 phase, so two types of vanadium species (VO x and CeVO 4 ) are dispersed on the surface of cerium dioxide.…”
Section: Performance Improvement Of Vanadium Based Catalystsmentioning
confidence: 99%
“…11 Vanadium-based oxides have been studied for catalytic conversion of hydrocarbons into H 2 and hydrocarbon commodities at temperatures lower than those of typical thermochemical processes. [12][13][14][15][16] For instance, partial oxidation of methane to formaldehyde has been reported at temperatures 500-640 C with insights into the mechanism of sequential oxidation of methane. [17][18][19] Recently, Fu et al reported thermodynamic analysis of vanadia redox materials for thermochemical ammonia production with high fuel selectivity and a high solar-to-fuel efficiency of up to 38.1% is achieved.…”
Section: Introductionmentioning
confidence: 99%