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Vanadium oxide surfaces and supported vanadium oxide nanoparticles

MPS-Authors
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Guimond,  Sebastien
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Abu Haija,  Mohammad
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Kaya,  Sarp
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Lu,  Junling
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Weissenrieder,  Jonas
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Shaikhutdinov,  Shamil
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Kuhlenbeck,  Helmut
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Freund,  Hans-Joachim
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Citation

Guimond, S., Abu Haija, M., Kaya, S., Lu, J., Weissenrieder, J., Shaikhutdinov, S., et al. (2006). Vanadium oxide surfaces and supported vanadium oxide nanoparticles. Topics in Catalysis, 38, 117-125. doi:10.1007/s11244-006-0076-8.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-03CC-5
Abstract
The information obtained from the characterization of vanadium oxide single crystal surfaces is related to the study of vanadia nanoparticles supported on silica and alumina thin films, model systems for the so-called “supported monolayer vanadia catalysts”. It is found that these particles have properties similar to V2O3 surfaces, where the topmost V ions are involved in vanadyl groups and have a 5+ oxidation state. A vibrational spectroscopy investigation combined with DFT calculations show that the accepted interpretation of vibrational spectra from vanadia catalysts must be revised.