We present the results of a high-resolution neutron diffraction experiment with a fully deuterated methane hydrate type I at temperatures of 2, 100, and 150 K. Precise crystallographic parameters of the ice-like D2O lattice and the thermal parameters of the encaged methane molecules have been obtained. The parameters of the host lattice differ only slightly from values found for hydrates with asymmetric guests included, which leads to the conclusion that the host lattice of structure I is only a little adaptive. At low temperatures (2 K) the methane molecules in both types of cages present in structure I occupy positions in the center of the cages. At higher temperatures the thermal parameters in both types of cages reflect the surrounding cage geometries or more precisely the translational potentials of the cages. The orientational scattering length density of the CD4 molecules has been analyzed in terms of a multipole expansion with symmetry adapted functions [Press and Hüller, Acta Crystallogr., Sect. A: Cryst. Phys., Diffr., Theor. Gen. Crystallogr. A29, 252 (1972); Press, ibid. A29, 257 (1972)]. In both types of cages we found only small modulations of a spherically symmetric scattering density accounting for almost free rotations of the methane molecules. The large and asymmetric cage leads to a somewhat more pronounced modulation of the orientational density than in the small dodecahedral cage. The orientational probability distribution function (PDF) remains nearly unchanged from 2 to 150 K. At 200 K we observed the time-resolved decomposition of the hydrate structure I into hexagonal ice Ih.

In this paper it is shown that diffuse-scattering experiments within the region of total external reAection can be explained quantitatively using the distorted-wave Born approximation for layer systems. Three Si/Ge samples with different degrees of complexity were investigated. The simultaneous analysis of the specular rejected intensity and the diffuse scattering leads to one consistent set of interface and layer parameters, which is able to fit both the shapes and the locations of all dynamic peaks in the off-specular scans and the characteristics of the rejected intensity. Therefore the distorted-wave Born approximation seems to give a correct and complete description of the diffuse scattering in the region of total external reflection.

The thermal conductivity of a gas hydrate is much lower than that of ice and more intriguingly, in spite of the crystalline structure, the temperature profile resembles an amorphous solid. Here we present results from neutron incoherent inelastic scattering (IINS) experiments and theoretical relaxation time calculations to demonstrate unambiguously the coupling of guest and water framework vibrations. The coupling is the consequence of symmetry forbidden crossings of the localized guest motions with the acoustic branches of the lattice vibrations. This phonon interaction leads to an energy exchange mechanism that explains the anomalous thermal behaviour.

dR ~' d~ P({~,R.},{~,Rj};t) wi'~ E ~ E,Rj})Here P({m~;Rj},{m~;Rj}';t)dj is the density matrix of the molecular crystal. Again the prime in (2.5) means that integration over m~ for j = I should be omitted. 3 Usually it is impossible to handle the above expression and approximations are required, e.g., the replacement of P by a product of single particle density matrices (Hartree approximation /2.9/).

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Methane is the simplest organic molecule, and like many supposedly simple molecular materials it has a rich phase diagram. While crystal structures could be determined for two of the solid phases, that of the low temperature phase III remained unsolved. Using high-resolution neutron powder diffraction and a direct-space Monte Carlo simulated annealing approach, this fundamental structure has now finally been solved. It is orthorhombic with space group Cmca, and 16 molecules in the unit cell. The structure is closely related to that of phase II, yet is no subgroup of it.

The structure of succinonitrile in its orientationally disordered phase was reexamined through extended X-ray diffraction measurements. It was solved by using both the analytic procedures of symmetry-adapted functions and a Frenkel model assuming discrete orientations. A possible translation-rotation coupling was included in this latter case via an offset vector e. The study confirms that the nitrogen atoms are localised along the fourfold axis of the cubic cell but evidences a strong offset of the centre of mass for gauche conformations. It is shown that this can be explained by steric hindrance between some configurations of neighbouring molecules.

The anomalous glass-like thermal conductivity of crystalline clathrates has been suggested to be the result of the scattering of thermal phonons of the framework by 'rattling' motions of the guests in the clathrate cages. Using the site-specific (83)Kr nuclear resonant inelastic scattering spectroscopy in combination with conventional incoherent inelastic neutron scattering and molecular-dynamics simulations, we provide unambiguous evidence and characterization of the effects on these guest-host interactions in a structure-II Kr clathrate hydrate. The resonant scattering of phonons led to unprecedented large anharmonic motions of the guest atoms. The anharmonic interaction underlies the anomalous thermal transport in this system. Clathrates are prototypical models for a class of crystalline framework materials with glass-like thermal conductivity. The explanation of the unusual molecular dynamics has a wide implication for the understanding of the thermal properties of disordered solids and structural glasses.