The nonlinear dielectric relaxation ac stationary response of an assembly of rigid polar molecules acted on by strong superimposed external dc E0 and ac E1(t)=E(1) cos omegat electric fields is evaluated in the context of the noninertial rotational diffusion model. The calculation proceeds by expanding the relaxation functions f(n)(t) (the expectation value of the Legendre polynomials P(n)), which describe the nonlinear relaxation of the system, as a Fourier series in the time domain. Hence, an infinite hierarchy of recurrence equations for the Fourier components of f(n)(t) is obtained. The exact solution of this hierarchy can be obtained in terms of a matrix continued fraction, so allowing us to evaluate the ac nonlinear response. For a weak ac field our results are in complete agreement with previous solutions obtained by perturbation methods. Diagrams showing the behavior of the in-phase and out-of-phase components of the electric polarization are presented.
We address the issue of inter-particle dipolar interactions in the context of magnetic hyperthermia. More precisely, the main question dealt with here is concerned with the conditions under which the specific absorption rate is enhanced or reduced by dipolar interactions. For this purpose, we propose a theory for the calculation of the AC susceptibility, and thereby the specific absorption rate, for a monodisperse two-dimensional assembly of nanoparticles with oriented anisotropy, in the presence of a DC magnetic field, in addition to the AC magnetic field. We also study the competition between the dipolar interactions and the DC field, both in the transverse and longitudinal configurations. In both cases, we find that the specific absorption rate has a maximum at some critical DC field that depends on the inter-particle separation. In the longitudinal setup, this critical field falls well within the range of experiments.
Based on the temperature behavior of the entropy increment induced by the probing electric field in the isotropic phase of mesogenic compounds belonging to the homologous series C(n)H(2n+1)PhCOOPhCN ( n = 4-10), it is found that an ability to the dipolar aggregation of the molecules depends on the alkyl tail length, and, in particular, the ability is strongly reinforced when the number n changes from 7 to 8. The role of the molecular structure in the self-assembling process is discussed.
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