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  Nitric Oxide Adsorption and Oxidation on SBA-15 Supported Molybdenum Oxide: A Transmission IR Study

Thielemann, J. P., Kröhnert, J., & Hess, C. (2010). Nitric Oxide Adsorption and Oxidation on SBA-15 Supported Molybdenum Oxide: A Transmission IR Study. Journal of Physical Chemistry C, 114(40), 17092-17098. doi:10.1021/jp1038046.

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 Creators:
Thielemann, Jörg P.1, Author           
Kröhnert, Jutta1, Author           
Hess, Christian, Author
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Free keywords: molybdenum oxide, supported; SBA-15; nitrate; nitric oxide; adsorption; IR Research Context: molybdenum oxide supported on silica SBA-15
 Abstract: The formation of NO and nitrate adsorbates on supported metal oxides is a valuable tool to gain insight into the coordination geometry and connectivity of surface metal oxide species. In this study, dispersed molybdenum oxide supported on silica SBA-15 with loadings of 5.9 wt % Mo (0.8 Mo/nm2) and 10.2 wt % Mo (2.2 Mo/nm2) has been investigated in detail by transmission IR spectroscopy using NO adsorption and oxidation. The treatment of the reduced 5.9 wt % Mo (0.8 Mo/nm2) MoxOy/SBA-15 with NO leads to the formation of molybdenum dinitrosyl complexes [Mo4+−(NO)2]. The use of isotopically labeled 15NO causes a shift of the 14NO dinitrosyl bands from 1806 and 1702 cm−1 to 1779 and 1682 cm−1, respectively. Higher oxidized nitrogen oxide species, which are formed in the presence of a 14NO/O2 mixture, have been studied on oxidized and reduced 5.9 wt % Mo (0.8 Mo/nm2) MoxOy/SBA-15. Two nitrogen oxide bands are stable toward evacuation and moderate temperature treatment. The presence of 15NO/O2 leads to shifts of these bands from 1618 to 1585 cm−1 and from 1573 to 1534 cm−1. A similar behavior is observed for the higher-loaded sample with 10.2 wt % Mo (2.2 Mo/nm2). As interference with other NO oxidation products and water can be excluded, the bands are assigned to bridging and bidentate surface nitrates, respectively.

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Language(s): eng - English
 Dates: 2010-08-25
 Publication Status: Issued
 Pages: -
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 Rev. Type: Peer
 Identifiers: eDoc: 498657
DOI: 10.1021/jp1038046
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Title: Journal of Physical Chemistry C
  Alternative Title : J. Phys. Chem. C
Source Genre: Journal
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Pages: - Volume / Issue: 114 (40) Sequence Number: - Start / End Page: 17092 - 17098 Identifier: -