Role of structure in the α and β dynamics of a simple glass-forming liquid

The elusive connection between dynamics and local structure in supercooled liquids is an important piece of the puzzle in the unsolved problem of the glass transition. The Johari-Goldstein β relaxation, ubiquitous in glass-forming liquids, exhibits mean properties that are strongly correlated to the long-time α dynamics. However, the former comprises simpler, more localized motion, and thus has perhaps a more straightforward connection to structure. Molecular dynamics simulations were carried out on a two-dimensional, rigid diatomic molecule (the simplest structure exhibiting a distinct β process) to assess the role of the local liquid structure on both the Johari-Goldstein β and the α relaxation. Although the average properties for these two relaxations are correlated, there is no connection between the β and α properties of a given (single) molecule. The propensity for motion at long times is independent of the rate or strength of a molecule's β relaxation. The mobility of a molecule averaged over many initial energies, a measure of the influence of structure, was found to be heterogeneous, with clustering at both the β and α time scales. This heterogeneity is less extended spatially for the β than for the α dynamics, as expected; however, the local structure is the more dominant control parameter for the β process. In the glassy state, the arrangement of neighboring molecules determines entirely the relaxation properties, with no discernible effect from the particle momenta.