On the structure of vanadium oxide supported on aluminas

UV and visible Raman spectroscopy, UV-visible diffuse reflectance spectroscopy, and temperature-programmed reduction studies

Zili Wu, Hack Sung Kim, Peter C Stair, Sreekala Rugmini, S. David Jackson

Research output: Contribution to journalArticle

116 Citations (Scopus)

Abstract

Vanadia species on aluminas (δ and γ-Al 2O 3) with surface VO x density in the range 0.01-14.2 V/nm 2 have been characterized by UV and visible Raman spectroscopy, UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), and temperature-programmed reduction in hydrogen. It is shown that the alumina phase has little influence on the structure and reducibility of surface VO x species under either dehydrated or hydrated conditions. Three similar types of dispersed VO x species, i.e., monovanadates, polyvanadates, and V 2O 5, are identified on both aluminas under dehydrated conditions. Upon hydration, polymerized VO x species dominate on the surfaces of the two aluminas. The broad Raman band at around 910 cm -1, observed on dehydrated V/δ, γ-Al 2O 3 at all V loadings (0.01-14.2 V/nm 2), is assigned to the interface mode (V-O-Al) instead of the conventionally assigned V-O-V bond. The direct observation of the interface bond is of significance for the understanding of redox catalysis because this bond has been considered to be the key site in oxidation reactions catalyzed by supported vanadia. Two types of frequency shifts of the V=O stretching band (1013-1035 cm -1) have been observed in the Raman spectra of V/Al 2O 3: a shift as a function of surface VO x density and a shift as a function of excitation wavelength. The shift of the V=O band to higher wavenumbers with increasing surface VO, density is due to the change of VO x structure. The V=O stretching band in dispersed vanadia always appears at lower wavenumber in UV Raman spectra than in visible Raman spectra for the same V/Al 2O 3 sample. This shift is explained by selective resonance enhancement according to the UV-Vis DRS results. It implies that UV Raman has higher sensitivity to isolated and less polymerized VO x species while visible Raman is more sensitive to highly polymerized VO x species and crystalline V 2O 5. These results show that a multiwavelength excitation approach provides a more complete structural characterization of supported VO x catalysts.

Original languageEnglish
Pages (from-to)2793-2800
Number of pages8
JournalJournal of Physical Chemistry B
Volume109
Issue number7
DOIs
Publication statusPublished - Feb 24 2005

Fingerprint

Vanadium
vanadium oxides
Aluminum Oxide
Oxides
Raman spectroscopy
Alumina
aluminum oxides
Spectroscopy
reflectance
Raman scattering
spectroscopy
shift
Raman spectra
Stretching
Temperature
temperature
Vanadates
visible spectrum
Hydration
Catalysis

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

On the structure of vanadium oxide supported on aluminas : UV and visible Raman spectroscopy, UV-visible diffuse reflectance spectroscopy, and temperature-programmed reduction studies. / Wu, Zili; Kim, Hack Sung; Stair, Peter C; Rugmini, Sreekala; Jackson, S. David.

In: Journal of Physical Chemistry B, Vol. 109, No. 7, 24.02.2005, p. 2793-2800.

Research output: Contribution to journalArticle

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