Ab-initio theory of superconductivity

A. Sanna, A. Linscheid, C. Bersier, H. Glawe, A. Davydov, K. Dewhurst, F. Essenberger</</span>

The success of density functional theory (DFT) for electronic structure calculations is at the basis of modern theoretical condensed matter physics. The original theorem of Hohenberg and Kohn (HK) and the reproducibility of the exact electronic density in a non-interacting Kohn Sham (KS) system both extend to, in principle, any electronic phase, including magnetism and superconductivity. However the practical applicability of KS-DFT depends on the availability of density functionals for the relevant observables of the system. As a matter of fact to derive density functionals able to describe the features of symmetry broken phases, in particular the order parameter (OP) of that phase, turns out to be a task of outstanding complexity.

A scheme to circumvent this problem is to generalize the HK theorem to include the OP as an additional density. The corresponding KS system then reproduces both the electronic and the additional density. In the case of superconductivity the original formulation of a DFT scheme (SCDFT) is due to Oliveira, Gross and Kohn^[1] where the additional density is the order parameter of superconductivity χ(r,r') = 〈Ψ↑(r)Ψ↓(r')〉. With a further development of DFT to include the nuclear degrees of freedom^[2] , in recent years an approximate exchange correlation potential F_xc for the KS Bogoliubov-de-Gennes system has been derived which features the electron-phonon (e-ph) and the electron-electron (e-e) interaction on the same footing^[3].

This leads to a self-consistent equation for the superconducting OP that depends on the phononic features and on the normal-state electronic structure. In the space of single particle KS orbitals it is formally equivalent to a BCS gap equation

where n and k , respectively, are the electronic band index and the wave vector inside the Brillouin zone. β is the inverse temperature and

are the excitation energies of the KS system, defined in terms of the gap function Δ_nk and the KS eigenvalues ξ_nk measured with respect to the Fermi energy. The kernel, K, consists of two contributions K=K^e-ph+K^e-e, representing the effects of the e-ph and of the e-e interactions, respectively. The gap function is related to the the OP in the KS basis by

Compared to many-body perturbation theory, SCDFT features two major achievements: 1) It is completely free of adjustable parameters. Coulomb and phonon mediated interactions are included without the need of introducing a phenomenological μ^∗. 2) all the frequency summations are performed analytically in the construction of F_xc. Retardation effects can be exactly included but at the same time the gap equation has still the form of a static BCS equation. The formal simplicity of eq. 1 then allows to account for the anisotropy of real systems at a low computational cost.

At the Fermi energy (ξ_nk = 0) the form of Δ_nk is determined mostly by the attractive phononic term K^e-ph. Beyond the phononic energy range the interaction becomes repulsive due the direct Coulomb interaction between electrons in K^e-e. The system then maximizes its condensation energy by including a sign change in Δ_nk. In accordance with Eq. 1, when both the interaction and Δ_nk change sign, then the overall contribution becomes once again attractive. This mechanism takes the name Coulomb renormalization.

The typical behavior of Δ_nk versus ξ_nk is plotted in In Fig. 1. for graphane (hydrogenated graphene C₂H₂). We use a logarithmic scale to enhance the behavior at the Fermi energy. This system shows a characteristic two gap structure, i.e. Δ_nk at the Fermi energy shows two distinctly different values corresponding to the presence of two Fermi surfaces. A similar behaviour, but with three distinct gap values at the Fermi energy, is found for hydrogen under pressure. We predict that this material has a critical temperature 242 K at 450 GPa^[4].

The more anisotropic the Fermi surface and the electron phonon coupling are the more structured becomes the gap function at the Fermi energy. An example is CaC₆ shown in Fig. 2 where the superconducting gap closely reflects the phononic anisotropy^[5].

To go beyond this reciprocal space description, we have recently implemented a transformation of the superconducting OP χ_nk back into real space.

This means to multiply the KS basis {φ_nk(r)} of the initial expansion:

(2)

where R=(r+r')/2 and s=(r-r') are respectively the center of mass and the relative coordinate of the cooper pair. We are thereby able to connect the chemical bonding properties with superconducting features in a very graphic and compact way.

As an example we show χ(R,0) of CaC₆ and C₂H_c in Fig. 3 and Fig. 4, respectively. The electronic bonds giving the largest contribution to superconductivity are clearly visible. In graphane the large positive values come from the sp² carbon bonds. In CaC₆ the dominant contribution arises from the π-states as well as d_z² Ca orbitals and interlayer states. The Coulomb renormalization contributions is provided by the C-H bonds in graphane and by the sp² states of CaC₆ (blue regions).

References

[1]

L.N. Oliveira, E.K.U. Gross and W. Kohn, Phys. Rev. Lett. 60, 2430 (1988)

[2]

T. Kreibich and E.K.U. Gross Phys. Rev. Lett. 86 2984 (2001)

[3]

M. Lueders et al., Phys. Rev. B 72, 024545 (2005), M.A.L.  Marques et al., Phys. Rev. B 72, 024546 (2005)

[4]

P. Cudazzo, G. Profeta, A. Sanna, A. Floris, A. Continenza, S. Massidda, and E. K. U. Gross, Phys. Rev. Lett. 100, 257001 (2008), Phys. Rev. B 81, 134505 (2010), Phys. Rev. B 81, 134506 (2010)

[5]

A. Sanna, G. Profeta, A. Floris, A. Marini, E.K.U. Gross and S. Massidda, Phys. Rev. B 75, 020511 (2007)