First-principles wavevector- and frequency-dependent exchange-correlation kernel for jellium at all densities
Aaron D. Kaplan (1), Niraj K. Nepal (1), Adrienn Ruzsinszky (1),, Pietro Ballone (2), John P. Perdew (1) ((1) Temple University, (2) University, College, Dublin)

TL;DR
This paper develops a nonlocal exchange-correlation kernel for jellium that accurately captures correlation energies across all densities and satisfies known physical constraints, improving upon previous models.
Contribution
The authors introduce a revised MCP07 kernel that incorporates frequency dependence and satisfies additional exact constraints for jellium at all densities.
Findings
Kernel accurately describes correlation energies across densities.
Frequency dependence is crucial only at very low densities.
Predicted ultranonlocality coefficient is negligible for Al and Na.
Abstract
We propose a spatially and temporally nonlocal exchange-correlation (xc) kernel for the spin-unpolarized fluid phase of ground-state jellium, for use in time-dependent density functional and linear response calculations. The kernel is constructed to satisfy known properties of the exact xc kernel, to accurately describe the correlation energies of bulk jellium, and to satisfy frequency-moment sum rules at a wide range of bulk jellium densities, including those low densities that display strong correlation and symmetry breaking. These effects are easier to understand in the simple jellium model than in real systems. All exact constraints satisfied by the recent MCP07 kernel [A. Ruzsinszky, et al., Phys. Rev. B 101, 245135 (2020)] are maintained in the new revised MCP07 (rMCP07) kernel, while others are added. The revision differs from MCP07 only…
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