Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/84455
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dc.contributor.authorRaston, P.-
dc.contributor.authorKnapp, C.-
dc.contributor.authorJager, W.-
dc.date.issued2011-
dc.identifier.citationPhysical Chemistry Chemical Physics, 2011; 13(42):18789-18798-
dc.identifier.issn1463-9076-
dc.identifier.issn1463-9084-
dc.identifier.urihttp://hdl.handle.net/2440/84455-
dc.description.abstractWe report the infrared depletion spectrum of para- and ortho-hydrogen peroxide embedded in superfluid helium nanodroplets in the OH stretching region. Six transitions were observed in the antisymmetric stretching band (v5) of H2O2, and three in the weaker symmetric stretching band (v1). While rotations about the b- and c-axes are slowed by a factor of [similar]0.4 relative to the gas phase, rotations about the a-axis are not significantly affected; this relates to the rotational speed about the a-axis being too fast for helium density to adiabatically follow. The trans tunneling splitting does not appear to be considerably affected by the helium droplet environment, and is reduced by only 6% relative to the gas phase, under the assumption that the vibrational shifts of the v5 and v1 torsional subbands are the same. The linewidths increase with increasing rotorsional energies, and are significantly narrower for energies which fall within the “phonon gap” of superfluid helium. These narrower lines are asymmetrically broadened, indicative of a dynamical coupling between the H2O2 rotor and surrounding helium density.-
dc.description.statementofresponsibilityPaul L. Raston, Chrissy J. Knapp and Wolfgang Jäger-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsCopyright status unknown-
dc.source.urihttp://dx.doi.org/10.1039/c1cp21348b-
dc.titleRotovibrational spectroscopy of hydrogen peroxide embedded in superfluid helium nanodroplets-
dc.typeJournal article-
dc.identifier.doi10.1039/C1CP21348B-
pubs.publication-statusPublished-
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