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Neutron Vibrational Spectroscopy of the H5O2+ Ion and Its Deuterated Analog in Phosphotungstic Acid Hexahydrate

Published online by Cambridge University Press:  10 February 2011

N. C. Maliszewskyj ,
T. J. Udovic  and
J. M. Nicol
N. C. Maliszewskyj
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA
T. J. Udovic*
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA
J. M. Nicol
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA
*
*To whom correspondence should be addressed
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Abstract

Heteropolyacid hydrates of the general form H3PM12O40. nH2O are of interest to researchers in areas such as proton conductivity and catalysis. The water molecules in these hydrated acids reside in the interstitial volume between the large Keggin anions and can, under certain conditions, complex with the acidic protons to form stable cations such as the “dioxonium” ion (H5O2+). We have used incoherent inelastic neutron scattering (IINS) measurements of dodecatungstophosphoric acid hexahydrate (H3PW12O40 · 6H2O) to obtain the vibrational density of states spectrum of H5O2+ stabilized by the PW12O403− Keggin anions. Spectra were measure for fully hydrogenated and fully deuterated ions in order to determine the relative merit of previous assignments of the normal mode vibrations.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 431: Symposium P – Microporous and Macroporous Materials , 1996 , 203
Copyright
Copyright © Materials Research Society 1996

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Footnotes

†

Present Address: MOLTECH Corp., Bldg. 061, 9000 South Rita Rd., Tucson, AZ 85747

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