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Raman spectroscopy of monolayer-type oxide catalysts: Supported Mo oxides

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TLDR
In this paper, a monolayer catalysts based on a structural model which assumed spreading of the active oxide over the support surface were investigated by a variety of techniques, conventional bulk sampling techniques as well as by surface-sensitive electron and ion spectroscopies, in an attempt to elucidate the nature of the catalyst surface species, and to study the coordination environment of active metal center(s).
Abstract
Oxides of the group VIb metals (Cr, Mo, W) and oxides of vanadium, rhenium, and niobium supported on a second high-surface-area metal oxide such as Al2O3, TiO2, Si02, ZrO2, and so forth are recognized as industrially important catalysts or catalyst precursors for various reactions [1–11], These materials frequently have been described as so-called monolayer catalysts based on a structural model which assumed spreading of the active oxide over the support surface. These catalysts have been investigated by a variety of techniques, conventional bulk sampling techniques as well as by surface-sensitive electron and ion spectroscopies, in an attempt to elucidate the nature of the catalyst surface species, and to study the coordination environment of the active metal center(s). Electronic spectroscopy gives rise to broad bands and the spectra are less informative than vibrational spectra. In addition, although techniques such as Auger electron spectroscopy (AES) and x-ray photoelectron spectroscopy (XPS...

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Citations
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Journal ArticleDOI

Raman spectroscopy of molybdenum oxides

TL;DR: In this paper, the resonance Raman detection of reduced molybdenum oxide phases is discussed in the above mentioned context of their active role in catalytic partial oxidation reactions. But this work was performed with a special sample of MoO2, which contained MoO 2, Mo4O11 and MoO3.
Journal ArticleDOI

Molecular structures of supported metal oxide catalysts under different environments

TL;DR: In this paper, the use of in situ Raman spectroscopy to study the molecular structures of supported metal oxide catalysts under different environments is reviewed and the effect of moisture at elevated temperatures is also discussed with regard to its implications for catalytic phenomena.
Journal ArticleDOI

Structure and properties of oxidative dehydrogenation catalysts based on MoO3/Al2O3

TL;DR: In this paper, the effects of MoOx structure on propane oxidative dehydrogenation (ODH) rates and selectivity were examined on Al2O3-supported molybdenum oxide catalysts with a wide range of Mo surface density (0.4-12 Mo/nm2).
Journal ArticleDOI

Micro-Raman study of the m-MoO2 to α-MoO3 transformation induced by cw-laser irradiation

TL;DR: In this paper, the authors report the monoclinic-MoO2 to orthorhombic -MoO3 transformation induced by continuous wave-laser irradiation.
Journal ArticleDOI

Characterization of Various Oxygen Species on an Oxide Surface: RuO2(110) †

TL;DR: The stoichiometric RuO2(110) surface is terminated by bridge-coordinated oxygen atoms (Oβ) and by coordinatively unsaturated Ru (Rucus) atoms Exposure to gaseous O2 leads to the formation of two additional surface species: a molecularly chemisorbed state (Oδ) bridging two neighboring Rucus atoms and weakly held Oγ) in terminal position above the RUCus atoms as discussed by the authors.
References
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Book

Infrared and Raman Spectra of Inorganic and Coordination Compounds

TL;DR: In this article, the normal modes of vibration are illustrated and corresponding vibrational frequencies are listed for each type, including diatomic, triatomic, fouratomic, five-atomic, six-atomic and seven-atomic types.
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TL;DR: In this article, the transition elements involving metal-metal bonds are defined and an introductory essay is given, along with a discussion of homogeneous catalysis and transition metal chemistry, B L Shaw & N I Tucker.
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Catalysis: Science and Technology

TL;DR: In early spring 1996, this article published a complete handbook on science and technology of catalysis, which is available as a set for a reduced price for all scientists working in the fields of kinetics and homogenous or heterogenous catalysis.
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