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Infrared study of ozone adsorption on TiO2 (anatase). / Bulanin, K. M.; Lavalley, J. C.; Tsyganenko, A. A.

In: Journal of Physical Chemistry, Vol. 99, No. 25, 01.01.1995, p. 10294-10298.

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Harvard

Bulanin, KM, Lavalley, JC & Tsyganenko, AA 1995, 'Infrared study of ozone adsorption on TiO2 (anatase)', Journal of Physical Chemistry, vol. 99, no. 25, pp. 10294-10298. https://doi.org/10.1021/j100025a034

APA

Vancouver

Bulanin KM, Lavalley JC, Tsyganenko AA. Infrared study of ozone adsorption on TiO2 (anatase). Journal of Physical Chemistry. 1995 Jan 1;99(25):10294-10298. https://doi.org/10.1021/j100025a034

Author

Bulanin, K. M. ; Lavalley, J. C. ; Tsyganenko, A. A. / Infrared study of ozone adsorption on TiO2 (anatase). In: Journal of Physical Chemistry. 1995 ; Vol. 99, No. 25. pp. 10294-10298.

BibTeX

@article{b68769f57e554975a0c87fe8f112d953,
title = "Infrared study of ozone adsorption on TiO2 (anatase)",
abstract = "Ozone adsorption at 77 K on titania (anatase) surface dehydrated at different temperatures or preexposed to pyridine, acetonitrile, and CO has been studied by infrared spectroscopy in order to characterize ozone interaction with Lewis acid sites of different strength. With weaker sites, ozone molecules form coordinative complexes bound via the terminal oxygen atom. The observed vibrational frequencies (about 1145 and 990 cm-1), as well as the isotopic shifts observed for ozone enriched by 18O, reveal a strong distortion of the molecule in this complex. No molecular adsorption of ozone on strong Lewis sites was detected. Data obtained provide evidence for ozone dissociation on these sites. Formation of atomic oxygen is suggested. It participates in oxidation of CO on the TiO2 surface.",
author = "Bulanin, {K. M.} and Lavalley, {J. C.} and Tsyganenko, {A. A.}",
year = "1995",
month = jan,
day = "1",
doi = "10.1021/j100025a034",
language = "English",
volume = "99",
pages = "10294--10298",
journal = "Journal of Physical Chemistry",
issn = "0022-3654",
publisher = "American Chemical Society",
number = "25",

}

RIS

TY - JOUR

T1 - Infrared study of ozone adsorption on TiO2 (anatase)

AU - Bulanin, K. M.

AU - Lavalley, J. C.

AU - Tsyganenko, A. A.

PY - 1995/1/1

Y1 - 1995/1/1

N2 - Ozone adsorption at 77 K on titania (anatase) surface dehydrated at different temperatures or preexposed to pyridine, acetonitrile, and CO has been studied by infrared spectroscopy in order to characterize ozone interaction with Lewis acid sites of different strength. With weaker sites, ozone molecules form coordinative complexes bound via the terminal oxygen atom. The observed vibrational frequencies (about 1145 and 990 cm-1), as well as the isotopic shifts observed for ozone enriched by 18O, reveal a strong distortion of the molecule in this complex. No molecular adsorption of ozone on strong Lewis sites was detected. Data obtained provide evidence for ozone dissociation on these sites. Formation of atomic oxygen is suggested. It participates in oxidation of CO on the TiO2 surface.

AB - Ozone adsorption at 77 K on titania (anatase) surface dehydrated at different temperatures or preexposed to pyridine, acetonitrile, and CO has been studied by infrared spectroscopy in order to characterize ozone interaction with Lewis acid sites of different strength. With weaker sites, ozone molecules form coordinative complexes bound via the terminal oxygen atom. The observed vibrational frequencies (about 1145 and 990 cm-1), as well as the isotopic shifts observed for ozone enriched by 18O, reveal a strong distortion of the molecule in this complex. No molecular adsorption of ozone on strong Lewis sites was detected. Data obtained provide evidence for ozone dissociation on these sites. Formation of atomic oxygen is suggested. It participates in oxidation of CO on the TiO2 surface.

UR - http://www.scopus.com/inward/record.url?scp=33751155308&partnerID=8YFLogxK

U2 - 10.1021/j100025a034

DO - 10.1021/j100025a034

M3 - Article

AN - SCOPUS:33751155308

VL - 99

SP - 10294

EP - 10298

JO - Journal of Physical Chemistry

JF - Journal of Physical Chemistry

SN - 0022-3654

IS - 25

ER -

ID: 41684946