We present an in-depth description of the methodology for accurate quantum calculation of the inelastic neutron scattering (INS) spectra of an H 2 molecule confined inside a nanosize cavity of an arbitrary shape. This methodology was introduced in a recent work, where the INS spectra of para- and ortho-H2 in the small cage of the structure II clathrate hydrate were simulated and compared with the measured spectra. The key distinctive feature of our approach, and its main strength and advantage, is the use of the coupled quantum 5D translation-rotation (TR) energy levels and wave functions of the entrapped H2 molecule, rigorously calculated on the 5D intermolecular potential energy surface (PES), as the initial and the final states of the INS transitions. In this work, we describe the implementation of the 5D TR wave functions within the quantum INS formalism, and obtain the working expressions for the matrix elements required to compute the INS spectra of the nanoconfined H2 molecule. The computational approach devised for efficient calculation of the 5D TR eigenstates in the compact contracted basis, indispensable for our quantum simulation of the INS spectra, is presented as well. Since the TR coupling is fully taken into account, the computed INS spectra exhibit a uniquely high degree of realism and faithfully reflect the quantum dynamics of H2 on the PES of the host environment.
|Original language||English (US)|
|Journal||Physical Review B - Condensed Matter and Materials Physics|
|State||Published - Nov 18 2011|
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Condensed Matter Physics