Dynamic arrest in a liquid of symmetric dumbbells: reorientational hopping for small molecular elongations.
نویسندگان
چکیده
We present extensive equilibrium and out-of-equilibrium molecular-dynamics simulations of a liquid of symmetric dumbbell molecules, for constant packing fraction, as a function of temperature and molecular elongation. We compute diffusion constants as well as odd and even orientational correlators. The notations odd and even refer to the parity of the order l of the corresponding Legendre l polynomial, evaluated for the orientation of the molecular axis relative to its initial position. Rotational degrees of freedom of order l are arrested if, in the long-time limit, the corresponding orientational l correlator does not decay to zero. It is found that for large elongations translational and rotational degrees of freedom freeze at the same temperature. For small elongations only the even rotational degrees of freedom remain coupled to translational motions and arrest at a finite common temperature. On the contrary, the odd rotational degrees of freedom remain ergodic at all investigated temperatures. Hence, in the translationally arrested state, each molecule remains trapped in the cage formed by its neighboring molecules, but is able to perform 180 degrees rotations, which lead to relaxation only for the odd orientational correlators. The temperature dependence of the characteristic time of these residual rotations is well described by an Arrhenius law. Finally, we discuss the evidence in favor of the presence of the type-A transition for the odd rotational degrees of freedom, as predicted by mode-coupling theory for small molecular elongations. This transition is distinct from the type-B transition, associated with the arrest of the translational and even rotational degrees of freedom for small elongations, and with all degrees of freedom for large elongations. Odd orientational correlators are computed for small elongations at very low temperatures in the translationally arrested state. The obtained results suggest that hopping events restore the ergodicity of the odd rotational degrees of freedom at temperatures far below the A transition.
منابع مشابه
Reorientational relaxation of a linear probe molecule in a simple glassy liquid.
Within the mode-coupling theory (MCT) for the evolution of structural relaxation in glass-forming liquids, correlation functions and susceptibility spectra are calculated characterizing the rotational dynamics of a top-down symmetric dumbbell molecule, consisting of two fused hard spheres immersed in a hard-sphere system. It is found that for sufficiently large dumbbell elongations, the dynamic...
متن کاملRotational dynamics of axially symmetric solutes in isotropic liquids. I. A collective cage description from molecular dynamics simulations
An operational definition of collective cage variables previously introduced for liquid argon is extended, via a molecular dynamics study, to the rotational properties of axially symmetric molecules. Quantitative measures of the static and dynamic cage properties are extracted for liquid Cl2 near the triple point. The collective cage variables are well described by the potential acting on an ar...
متن کاملTheory for the reorientational dynamics in glass-forming liquids
The mode-coupling theory for ideal liquid-glass transitions is extended so that the structural relaxation for the reorientational degrees of freedom of a linear molecule, which is immersed in a system of spherical particles, can be described. Closed equations of motion for the correlation functions formed with tensor density fluctuations are derived, which deal with the molecule’s translational...
متن کاملThermo-molecular orientation effects in fluids of dipolar dumbbells.
We use molecular dynamics simulations in applied thermal gradients to study thermomolecular orientation (TMO) of size-asymmetric dipolar dumbbells with different molecular dipole moments. We find that the direction of the TMO is the same as in apolar dumbbells of the same size, i.e. the smaller atom in the dumbbell tends to orient towards the colder temperature. The ratio of the electrical pola...
متن کاملEffect of the local hydrogen bonding network on the reorientational and translational dynamics in supercritical water.
Molecular dynamics simulations have been performed in a wide range of densities along a near critical isotherm of supercritical water in order to reveal the interconnection between the local hydrogen bonding (HB) network and several related dynamic properties. The results obtained have revealed a significant slowing down of reorientational dynamics of the water molecules as the value of the num...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The Journal of chemical physics
دوره 123 20 شماره
صفحات -
تاریخ انتشار 2005