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Physical Review B

Time-dependent density functional theory: Derivation of gradient-corrected dynamical exchange-correlational potentials

Jianmin Tao, Giovanni Vignale, I. V. Tokatly

Published Nov 30, 2007• 21 citations
Publisher

Abstract

We have recently proposed an approximation for the dynamical exchange-correlation (XC) potentials of time-dependent current-density functional theory beyond the local density approximation [Phys. Rev. Lett. 97, 036403 (2006)]. The novel feature of the approximation is that the dependence of the dynamical XC potentials upon the density gradient and other inhomogeneity parameters (e.g., the Laplacian of the density and the kinetic energy density) is introduced by applying the generalized gradient approximation (GGA) and meta-GGA to the calculation of the XC stress tensor. The scheme may allow a more accurate treatment of the dynamical properties of an inhomogeneous system, while reducing to the exact form for slowly varying densities and slowly varying external potentials. In this work, we present in detail the derivation of this XC potential, spell out the underlying assumptions, and explain their physical basis.

DOI
10.1103/physrevb.76.195126

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We have recently proposed an approximation for the dynamical exchange-correlation (XC) potentials of time-dependent current-density functional theory beyond the local density approximation [Phys. Rev. Lett. 97, 036403 (2006)]. The novel feature of the approximation is that the dependence of the dynamical XC potentials upon the density gradient and other inhomogeneity parameters (e.g., the Laplacian of the density and the kinetic energy density) is introduced by applying the generalized gradient approximation (GGA) and meta-GGA to the calculation of the XC stress tensor. The scheme may allow a more accurate treatment of the dynamical properties of an inhomogeneous system, while reducing to the exact form for slowly varying densities and slowly varying external potentials. In this work, we present in detail the derivation of this XC potential, spell out the underlying assumptions, and explain their physical basis.
Approximations for the ground-state exchange-correlation potential of density-functional theory have reached a high level of sophistication. By contrast, time- or frequency-dependent exchange-correlation potentials are still being treated in a local approximation. Here we propose a novel approximation scheme, which effectively brings the power of the generalized gradient approximation (GGA) and meta-GGA to time-dependent density-functional theory. The theory should allow a more accurate treatment of strongly inhomogeneous electronic systems (e.g. molecular junctions) while remaining essentially exact for slowly varying densities and slowly varying external potentials.
I review recent advances in understanding the physical character of the exchange-correlation (xc) potential in time-dependent density functional theory. I show that in an electron gas of slowly varying density the dynamical part of the xc potential is an extremely nonlocal functional of the density. This difficulty can be circumvented by introducing an xc vector potential that is a function of the local current density. The form of this vector potential is entirely specified by symmetry. Its physical effects are analogous to those of the viscous force in the Navier-Stokes equation of classical hydrodynamics. Recent applications of the xc vector potential to the calculation of infrared absorption linewidths in quantum wells are described.
Using Landau Fermi-liquid theory we derive a nonlinear nonadiabatic approximation for the exchange-correlation (xc) vector potential defined by the xc stress tensor. The stress tensor is a local nonlinear functional of two basic variables: the displacement vector and the second-rank tensor which describes the evolution of momentum in a local frame moving with Eulerian velocity. For irrotational motion and the equilibrium initial state the dependence on the tensor variable reduces to that on the metrics generated by dynamical deformation of the system.
The scalar f(xc) and tensor f(xc) exchange-correlation (xc) kernels are key ingredients of the time-dependent density functional theory and the time-dependent current density functional theory, respectively. We derive a comparatively simple relation between these two kernels under the assumption that the dynamic xc can be considered "weak." A calculation of the frequency-dependent dielectric function of silicon using this relation in conjunction with Vignale-Kohn f(xc) demonstrates a potential of our method to account for the dynamic many-body effects within the rigorous scheme of time-dependent density functional theory. Our formula provides a bridge between the scalar f(xc), which directly enters many applications, and the tensor f(xc) which, due to its locality in space, is much easier to approximate.
We propose a memory form of exchange-correlation potential vXC(r,t){v}_{\mathrm{XC}}(\mathbf{r},t)vXC​(r,t) for time-dependent interacting many-particle systems. Unlike previous memory-XC potentials, our vXC{v}_{\mathrm{XC}}vXC​ is not limited to the linear response regime. The proposed form of vXC{v}_{\mathrm{XC}}vXC​ is a generalized local-density approximation chosen so as to satisfy the nonlinear harmonic potential theorem and Newton's third law. For the case of the inhomogeneous electron gas, we give an explicit prescription for vXC{v}_{\mathrm{XC}}vXC​ based solely on an existing parametrization of the linear XC response kernel ${f}_{\mathrm{XC}}^{\mathrm{hom}}(n,\ensuremath{\omega})$ of the uniform gas. Application to quantum wells seems promising.
Time-dependent density-functional theory (TDDFT) treats dynamical exchange and correlation (xc) via a single-particle potential, Vxc(r,t){V}_{\mathrm{xc}}(\mathbf{r},t)Vxc​(r,t), defined as a nonlocal functional of the density $n({\mathbf{r}}^{\ensuremath{'}},{t}^{\ensuremath{'}})$. The popular adiabatic local-density approximation (ALDA) for Vxc(r,t){V}_{\mathrm{xc}}(\mathbf{r},t)Vxc​(r,t) uses only densities at the same space-time point (r,t)(\mathbf{r},t)(r,t). To go beyond the ALDA, two local approximations have been proposed based on quantum hydrodynamics and elasticity theory: (a) using the current as the basic variable (C-TDDFT) [G. Vignale, C. A. Ullrich, and S. Conti, Phys. Rev. Lett. 79, 4847 (1997)], (b) working in a comoving Lagrangian reference frame (L-TDDFT) [I. V. Tokatly, Phys. Rev. B 71, 165105 (2005)]. In this paper we illustrate, compare, and analyze both nonadiabatic theories for simple time-dependent model densities in the linear and nonlinear regime, for a broad range of time and frequency scales. C- and L-TDDFT are identical in certain limits, but, in general, exhibit qualitative and quantitative differences in their respective treatment of elastic and dissipative electron dynamics. In situations where the electronic density rapidly undergoes large deformations, it is found that nonadiabatic effects can become significant, causing the ALDA to break down.