Abstract

We review the theory and application of adiabatic exchange–correlation (xc)-kernels for ab initio calculations of ground state energies and quasiparticle excitations within the frameworks of the adiabatic connection fluctuation dissipation theorem and Hedin’s equations, respectively. Various different xc-kernels, which are all rooted in the homogeneous electron gas, are introduced but hereafter we focus on the specific class of renormalized adiabatic kernels, in particular the rALDA and rAPBE. The kernels drastically improve the description of short-range correlations as compared to the random phase approximation (RPA), resulting in significantly better correlation energies. This effect greatly reduces the reliance on error cancellations, which is essential in RPA, and systematically improves covalent bond energies while preserving the good performance of the RPA for dispersive interactions. For quasiparticle energies, the xc-kernels account for vertex corrections that are missing in the GW self-energy. In this context, we show that the short-range correlations mainly correct the absolute band positions while the band gap is less affected in agreement with the known good performance of GW for the latter. The renormalized xc-kernels offer a rigorous extension of the RPA and GW methods with clear improvements in terms of accuracy at little extra computational cost.

Highlights

  • Density functional theory (DFT) has been the workhorse of first-principles materials science

  • We have already shown that the random phase approximation (RPA) underestimates the correlation energy of the homogeneous electron gas (HEG) by 0.6–0.3 eV/electron, whereas the ALDA overestimates the correlation energy by 0.3 eV/electron compared to the RPA

  • We have reviewed the theory of xc-kernels derived from the HEG and illustrated how they can be used to obtain ground state correlation energies and QP band structures beyond the RPA and GW methods, respectively

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Summary

INTRODUCTION

Density functional theory (DFT) has been the workhorse of first-principles materials science. We show that the use of non-local (but in practice and involves other problems such as overestimated frequency-independent) kernels largely fixes the erroneous RPA band gaps and smeared out spectral features in GW and technical correlation hole and provides a much better description of short- difficulties associated with the self-consistent determination of the range correlations—at least for weakly correlated materials. Noting that χÃðr; r0; iωÞ 1⁄4 χðr[0]; r; iωÞ, we obtain

Z1 dλ dω 2π hhv c χ λ ðiωÞ v c χ 0 ðiωÞii:
RESULTS
CONCLUSIONS AND OUTLOOK
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