Search

The orientational dynamics of supercooled glycerol using molecular dynamics simulations for temperatures ranging from 323 K to 253 K, is probed through correlation functions of first and second ranks of Legendre polynomials, pertaining respectively to dielectric spectroscopy (DS) and depolarized dynamic light scattering (DDLS). The self, cross, and total correlation functions are compared with relevant experimental data. The computations reveal the low sensitivity of DDLS to cross-correlations, in agreement with what is found in experimental work, and strengthen the idea of directly comparing DS and DDLS data to evaluate the effect of cross-correlations in polar liquids. The analysis of the net static cross-correlations and their spatial decomposition shows that, although cross-correlations extend over nanometric distances, their net magnitude originates, in the case of glycerol, from the first shell of neighbouring molecules. Accessing the angular dependence of the static correlation allows us to get a microscopic understanding of why the rank-1 correlation function is more sensitive to cross-correlation than its rank-2 counterpart., Comment: 9 pages, 6 figures

An exact integral formula for the Kirkwood correlation factor of isotropic polar fluids $g_K$ is derived from the equilibrium averaged rotational Dean equation, which as compared to previous approaches easily lends itself to further approximations. The static linear permittivity of polar fluids $\epsilon$ is calculated as a function of temperature, density and molecular dipole moment in vacuo for arbitrary pair interaction potentials. Then, using the Kirkwood superposition approximation for the three-body orientational distribution function, we suggest a simple way to construct model potentials of mean torques considering permanent and induced dipole moments. We successfully compare the theory with the experimental temperature dependence of the static linear permittivity of various polar fluids such as a series of linear monohydroxy alcohols, water, tributyl phosphate, acetonitrile, acetone, nitrobenzene and dimethyl sulfoxide, by fitting only one single parameter, which describes the induction to dipole-dipole energy strength ratio. We demonstrate that comparing the value of $g_K$ with unity in order to deduce the alignment state of permanent dipole pairs, as is currently done is in many situations, is a misleading oversimplification, while the correct alignment state is revealed when considering the proper interaction potential. Moreover we show, that picturing H-bonding polar fluids as polar molecules with permanent and induced dipole moments without invoking any specific H-bonding mechanism is in many cases sufficient to explain experimental data of the static dielectric constant. In this light, the failure of the theory to describe the experimental temperature dependence of the static dielectric constant of glycerol, a non-rigid polyalcohol, is not due to the lack of specific H-bonding mechanisms, but rather to an oversimplified model potential for that particular molecule.

An analytical formula for the linear complex susceptibility of dipolar assemblies subjected to thermal agitation, long range interactions and an externally applied uniform sinusoidal field of weak amplitude is derived using the forced rotational diffusion equation of Cugliandolo et al. [Phys. Rev. E 91, 032139 (2015)] in the virial approximation. If the Kirkwood correlation factor of the dipolar assembly gK exceeds unity, a thermally activated process arising from the interaction-specific component arises while for gK<1, the susceptibility spectrum normalized by its static value is practically unaltered with respect to that of the ideal gas phase.

The Kirchhoff-Helmholtz principle of least heat dissipation is applied in order to derive the stationary state of the spin-Hall effect. Spin-accumulation due to spin-orbit interaction, spin-flip relaxation, and electrostatic interaction due to charge accumulation are treated on an equal footing. A nonlinear differential equation is derived, that describes both surface and bulk currents and spin-dependent chemical potentials. It is shown that if the ratio of the spin-flip relaxation length over the Debye-Fermi length is small, the stationary state is defined by a linear spin-accumulation potential and zero pure spin-current., Comment: 10 pages, 1 figure

The individual motion of a colloidal particle is described by an overdamped Langevin equation. When rotational degrees of freedom are relevant, these are described by a corresponding Langevin process. Our purpose is to show that the microscopic local density of colloids, in terms of a space and rotation state, also evolves according to a Langevin equation. The latter can then be used as the starting point of a variety of approaches, ranging from dynamical density functional theory to mode-coupling approximations.

The effect of long range dipole-dipole interactions on the thermal fluctuations of the magnetization of an assembly of single-domain ferromagnetic particles is considered. If orientational correlations between the particles are neglected, the evolution of the magnetization orientations may be described by a nonlinear Fokker-Planck equation (FPE) reducing to the usual linear one in the limit of infinite dilution [W.F. Brown Jr, Phys. Rev. 130, 1677 (1963)]. The thermally activated relaxation time scale of the assembly is estimated, leading to a simple modification of the axially symmetric asymptotes for the superparamagnetic relaxation time., Comment: 31 pages, 3 figures, regular article