TY - JOUR
T1 - Inelastic neutron scattering and raman light scattering from hydrogen-filled clathrates hydrates
AU - Ulivi, L.
AU - Celli, M.
AU - Giannasi, A.
AU - Ramirez-Cuesta, A. J.
AU - Zoppi, M.
PY - 2008
Y1 - 2008
N2 - Several samples of ternary tetrahydrofuran-H2O-H2 and binary H2O-H2 clathrate hydrates have been analysed by high-resolution inelastic neutron scattering and Raman light scattering. The neutron spectrum presents several intense bands due to H2 molecule excitations and in particular to rotational transitions, centre-of-mass translational transitions of either para-or ortho-H2, and to combinations of these. The H2 molecule behaves in the clathrate cage as an almost free rotor, and performs a translational motion (rattling), that is 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. Raman spectra show a similar splitting of the S0(0) rotational transition, due to a significant anisotropy of the potential with respect to the orientation of the molecule in the cage. The comparison of our experimental values for the transition frequencies to a recent quantum mechanical calculation is discussed.
AB - Several samples of ternary tetrahydrofuran-H2O-H2 and binary H2O-H2 clathrate hydrates have been analysed by high-resolution inelastic neutron scattering and Raman light scattering. The neutron spectrum presents several intense bands due to H2 molecule excitations and in particular to rotational transitions, centre-of-mass translational transitions of either para-or ortho-H2, and to combinations of these. The H2 molecule behaves in the clathrate cage as an almost free rotor, and performs a translational motion (rattling), that is 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. Raman spectra show a similar splitting of the S0(0) rotational transition, due to a significant anisotropy of the potential with respect to the orientation of the molecule in the cage. The comparison of our experimental values for the transition frequencies to a recent quantum mechanical calculation is discussed.
UR - http://www.scopus.com/inward/record.url?scp=84881230780&partnerID=8YFLogxK
U2 - 10.1088/1742-6596/121/4/042018
DO - 10.1088/1742-6596/121/4/042018
M3 - Conference article
AN - SCOPUS:84881230780
SN - 1742-6588
VL - 121
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
IS - PART 4
M1 - 042018
T2 - Joint 21st AIRAPT and 45th EHPRG International Conference on High Pressure Science and Technology
Y2 - 17 September 2007 through 21 September 2007
ER -