The local field factor $G(q)$ of the HEG describes how exchange and correlation modify the response to a static perturbation, and enters dielectric screening, effective electron--electron interactions, and the xc kernel of TDDFT. Accurate zero-temperature data for $G(q)$, however, remain limited to metallic densities, $r_s\leq10$. In this work, we present diffusion Monte Carlo calculations of the static density response function $\chi(q)$ and of $G(q)$ for $2\leq r_s\leq100$, and describe and discuss the methodological steps that enabled these calculations. We show how optimization of the perturbing potential in the trial wave function has an important effect, as a poor choice can reverse the sign of the response. A closed-form expression is provided for its optimal value, together with the density dependence of the linear-response window. We further show that backflow correlations leave $\chi(q)$ unchanged and that $G(q)$ depends only weakly on system size even at very low density, so that Slater--Jastrow wave functions and modest system sizes suffice. Together, these results provide a practical guide for future QMC calculations of response properties of the electron gas and real materials. Our results agree with previous DMC data at metallic densities for $q>k_F$, and extend them below $k_F$. They also agree with diagrammatic QMC at $r_s=2$. At lower densities, our results show that $G(q)$ develops a nonmonotonic structure at intermediate-$q$, where the response approaches that of the noninteracting gas. Quantitative agreement is seen with finite-temperature path integral Monte Carlo, suggesting that the previously reported finite-temperature structure is inherited from the ground state. Using a parametrization of $G(q)$ that reproduces our data throughout the liquid phase, we relate this structure to short-range order in the pair correlation function and the static structure factor.
The three-dimensional electron gas is a fundamental model in condensed matter physics and quantum chemistry, and the exchange-correlation energy derived from it serves as the starting point of \textit{ab initio} computations of materials. However, the wave-vector-dependent response, and hence the static local field fac...
Muhammed H. Güneş, Y. Yang, V. Gorelov et al.· 1 citation· ⚡1
We develop and implement the quadratic density response function of non-interacting fermions at arbitrary temperature, frequencies, and wave vectors. Starting from a Green's function formulation, we derive the quadratic response and demonstrate its equivalence to the result obtained from the Wigner equation. We further...
Pontus Svensson, J. Vorberger, Z. Moldabekov et al.· 0 citations
An old but recurring question in ground-state density functional theory, relevant to the construction of density functional approximations, is the existence of a second-order gradient expansion for the exchange energy that is exact for densities that vary slowly over space. Here we will argue that there is such an expa...
J. Perdew, Timo Lebeda, R. Maniar et al.· 1 citation· ⚡1
First-principles studies of materials with strong electronic correlations introduce additional theoretical complexities and computational costs, even more so if lattice degrees of freedom also play a role. To address these challenges, we show how direct and phonon-mediated electron-electron interactions can be treated...
J. Berges, Samuel Poncé, Mario Caserta et al.· 1 citation
Electronic spectra provide direct insight into the excitations and correlations of condensed matter systems. Their description requires electron correlations beyond mean field. In equilibrium, the $GW$ approximation has become the method of choice for many materials. Extending this approximation to nonequilibrium, howe...
Erik Schroedter, Jan-Philip Joost, Michael Bonitz et al.· 1 citation
Diffusion quantum Monte Carlo (DMC) and coupled cluster theory [CCSD(T)] are widely used benchmark methods for noncovalent interactions (NCIs). However, recent studies have reported notable discrepancies for several hydrogen-bonded and dispersion-dominated systems, raising questions about the accuracy of the approximat...
Kousuke Nakano, B. X. Shi, D. Alfé et al.· Journal of Chemical Physics· 1 citation
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.