arXiv subjects

Michael E. Fisher

Publications and source records attributed to Michael E. Fisher.

40 records · Page 3Linked to original sources

arXiv1997

Critique of Primitive Model Electrolyte Theories

Approximate theories for the restricted primitive model electrolyte are compared in the light of Totsuji's lower bound for the energy (an improvement over Onsager's), Gillan's upper bound for the free energy, and thermal stability requirements. Theories based on the Debye-Hueckel (DH) approach and the mean spherical approximation (MSA), including extensions due to Bjerrum, Ebeling, Fisher and Levin, and Stell, Zhou, and Yeh (PMSA1,2,3) are tested. In the range T* = (k_B T)Da/q^2 \lesssim 10 T*_c \simeq 0.5, all DH-based theories satisfy Totsuji's bound, while the MSA possesses a significant region of violation. Both DH and MSA theories violate Gillan's bound in the critical region and below unless ion pairing and the consequent free-ion depletion are incorporated. However, the PMSA theories, which recognize pairing but not depletion, fail to meet the bound. The inclusion of excluded-volume terms has only small effects in this respect. Finally, all the pairing theories exhibit negative constant-volume specific heats when T* \gtrsim 2T*_c \simeq 0.1; this is attributable to the treatment of the association constant.

cond-mat.stat-mech↗

arXiv1997

Charge Oscillations in Debye-Hueckel Theory

The recent generalized Debye-Hueckel (GDH) theory is applied to the calculation of the charge-charge correlation function G_{ZZ}(r). The resulting expression satisfies both (i) the charge neutrality condition and (ii) the Stillinger-Lovett second-moment condition for all T and rho_N, the overall ion density, and (iii) exhibits charge oscillations for densities above a "Kirkwood line" in the (rho_N,T) plane. This corrects the normally assumed DH correlations, and, when combined with the GDH analysis of the density correlations, leaves the GDH theory as the only complete description of ionic correlation functions, as judged by (i)-(iii), (iv) exact low-density (rho_N,T) variation, and (v) reasonable behavior near criticality.

cond-mat.stat-mech↗

arXiv1996

Ginzburg Criterion for Coulombic Criticality

To understand the range of close-to-classical critical behavior seen in various electrolytes, generalized Debye-Hueckel theories (that yield density correlation functions) are applied to the restricted primitive model of equisized hard spheres. The results yield a Landau-Ginzburg free-energy functional for which the Ginzburg criterion can be explicitly evaluated. The predicted scale of crossover from classical to Ising character is found to be similar in magnitude to that derived for simple fluids in comparable fashion. The consequences in relation to experiments are discussed briefly.

cond-mat↗

arXiv1996

Density Fluctuations in an Electrolyte from Generalized Debye-Hueckel Theory

Near-critical thermodynamics in the hard-sphere (1,1) electrolyte is well described, at a classical level, by Debye-Hueckel (DH) theory with (+,-) ion pairing and dipolar-pair-ionic-fluid coupling. But DH-based theories do not address density fluctuations. Here density correlations are obtained by functional differentiation of DH theory generalized to {\it non}-uniform densities of various species. The correlation length $ξ$ diverges universally at low density $ρ$ as $(Tρ)^{-1/4}$ (correcting GMSA theory). When $ρ=ρ_c$ one has $ξ\approxξ_0^+/t^{1/2}$ as $t\equiv(T-T_c)/T_c\to 0+$ where the amplitudes $ξ_0^+$ compare informatively with experimental data.

cond-mat↗