Self-consistent Overhauser model for the pair distribution function of an electron gas in dimensionalities D=3 and D=2

Details Self-consistent Overhauser model for the pair distribution function of an electron gas in dimensionalities D=3 and D=2 Self-consistent Overhauser model for the pair distribution function of an electron gas in dimensionalities D=3 and D=2

2002-01-23

arxiv.org/abs/cond-mat/0201423v2

Phys. Rev. B 66, 075110 (2002)

Physics

Condensed Matter

Strongly Correlated Electrons

14 pages, 7 figuers, to apear in Physical Review B

Scientific paper

10.1103/PhysRevB.66.075110

We present self-consistent calculations of the spin-averaged pair distribution function $g(r)$ for a homogeneous electron gas in the paramagnetic state in both three and two dimensions, based on an extension of a model that was originally proposed by A. W. Overhauser [Can. J. Phys. {\bf 73}, 683 (1995)] and further evaluated by P. Gori-Giorgi and J. P. Perdew [Phys. Rev. B {\bf 64}, 155102 (2001)]. The model involves the solution of a two-electron scattering problem via an effective Coulombic potential, that we determine within a self-consistent Hartree approximation. We find numerical results for $g(r)$ that are in excellent agreement with Quantum Monte Carlo data at low and intermediate coupling strength $r_s$, extending up to $r_s\approx 10$ in dimensionality D=3. However, the Hartree approximation does not properly account for the emergence of a first-neighbor peak at stronger coupling, such as at $r_s=5$ in D=2, and has limited accuracy in regard to the spin-resolved components $g_{\uparrow\uparrow}(r)$ and $g_{\uparrow\downarrow}(r)$. We also report calculations of the electron-electron s-wave scattering length, to test an analytical expression proposed by Overhauser in D=3 and to present new results in D=2 at moderate coupling strength. Finally, we indicate how this approach can be extended to evaluate the pair distribution functions in inhomogeneous electron systems and hence to obtain improved exchange-correlation energy functionals.

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