We present the results of a high-resolution inelastic neutron scattering experiment on three samples of ternary tetrahydrofuran clathrate hydrates, containing either H2 at different para/ortho concentrations, or HD. The spectrum due to the H2 molecule excitation shows spectral bands that are assigned unambiguously to rotational transitions, centre-of-mass translational transitions of either para- or ortho-H2, and to combinations of these. We demonstrate that the H2 molecule rotates almost freely, while performing a translational motion (rattling) in the cage, resulting in a paradigmatic example of the motion of a quantum particle in a non-harmonic three-dimensional potential well. Both the H2 rotational transition and the fundamental of the rattling transition split into triplets. This is a consequence of a significant anisotropy of the potential with respect to the orientation of the molecule in the cage, in the first case, or with respect to the centre-of-mass position inside the cage, in the second case. The comparison of our experimental values for the transition frequencies to a recent quantum mechanical calculation is discussed. Spectra obtained at different temperatures confirm an appreciable anharmonicity of the potential energy for the H2 molecule in the cage.
Inelastic neutron scattering from hydrogen clathrate hydrates
Ulivi L.;Celli M.;Giannasi A.;Zoppi M.
2008
Abstract
We present the results of a high-resolution inelastic neutron scattering experiment on three samples of ternary tetrahydrofuran clathrate hydrates, containing either H2 at different para/ortho concentrations, or HD. The spectrum due to the H2 molecule excitation shows spectral bands that are assigned unambiguously to rotational transitions, centre-of-mass translational transitions of either para- or ortho-H2, and to combinations of these. We demonstrate that the H2 molecule rotates almost freely, while performing a translational motion (rattling) in the cage, resulting in a paradigmatic example of the motion of a quantum particle in a non-harmonic three-dimensional potential well. Both the H2 rotational transition and the fundamental of the rattling transition split into triplets. This is a consequence of a significant anisotropy of the potential with respect to the orientation of the molecule in the cage, in the first case, or with respect to the centre-of-mass position inside the cage, in the second case. The comparison of our experimental values for the transition frequencies to a recent quantum mechanical calculation is discussed. Spectra obtained at different temperatures confirm an appreciable anharmonicity of the potential energy for the H2 molecule in the cage.| File | Dimensione | Formato | |
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