Diverging correlation lengths in electrolytes: Exact results at low densities

Abstract
The restricted primitive model of an electrolyte (equisized hard spheres carrying charges ±q0) is studied using Meeron’s expressions [J. Chem. Phys. 28, 630 (1958)] for the multicomponent radial distribution functions gστ(r;T,ρ), that are correct through terms of relative order ρ, the overall density. The exact second and fourth moment density-density correlation lengths ξN,1(T,ρ) and ξN,2(T,ρ), respectively, are thereby derived for low densities: in contrast to the Debye length ξD=(kBT/4πq02ρ)1/2, these diverge when ρ0 as (Tρ)1/4 and (T/ρ3)1/8, respectively, with universal amplitudes. The asymptotic expressions agree precisely with those obtained by Lee and Fisher [Phys. Rev. Lett. 76, 2906 (1996)] from a generalization of Debye-Hückel (GDH) theory to nonuniform ion densities. Other aspects of this GDH theory are checked and found to be exact at low densities. Specifically, with the further aid of the hypernetted-chain resummation, the corresponding charge-charge correlation lengths ξZ,1 and ξZ,2 and the Lebowitz length, ξL (which restricts charge fluctuations in large domains), are calculated up to nonuniversal terms of orders ρlnρ and ρ. In accord with the Stillinger-Lovett condition, one finds ξZ,1=ξD although the ratios ξZ,2/ξD and ξL/ξD deviate from unity at nonzero ρ.