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L. A. Constantin

Publications and source records attributed to L. A. Constantin.

22 records · Page 2Linked to original sources

Meta-GGA exchange-correlation functional with a balanced treatment of nonlocality

We construct a meta-generalized-gradient approximation which properly balances the nonlocality contributions to the exchange and correlation at the semilocal level. This non-empirical functional shows good accuracy for a broad palette of properties (thermochemistry, structural properties) and systems (molecules, metal clusters, surfaces and bulk solids). The accuracy for several well known problems in electronic structure calculations, such as the bending potential of the silver trimer and the dimensional crossover of anionic gold clusters, is also demonstrated. The inclusion of empirical dispersion corrections is finally discussed and analyzed.

physics.chem-ph↗

Spin-dependent gradient correction for more accurate atomization energies of molecules

We discuss, simplify, and improve the spin-dependent correction of L.A. Constantin et al., Phys. Rev. B 84, 233103, for atomization energies, and develop a density parameter of the form $v\propto |\nabla n|/n^{10/9}$, found from the statistical ensemble of one-electron densities. The here constructed exchange-correlation generalized gradient approximations (GGAs), named zvPBEsol and zvPBEint, show a broad applicability, and a good accuracy for many applications, because these corrected functionals significantly improve the atomization and binding energies of molecular systems, without worsening the behavior of the original functionals (PBEsol and PBEint) for other properties. This spin-dependent correction is also applied to meta-GGA dynamical correlation functionals combined with exact-exchange; in this case a significant (about 30%) improvement in atomization energies of small molecules is found.

physics.chem-ph↗

Testing the broad applicability of the PBEint GGA functional and its one-parameter hybrid form

We review the performance of the PBEint GGA functional (Phys. Rev. B 2010, 82, 113104) recently proposed to improve the description of hybrid interfaces, and we introduce its one-parameter hybrid form (hPBEint). We consider different well established benchmarks for energetic and structural properties of molecular and solid-state systems as well as model systems and newly developed benchmark sets for dipole moments and metal-molecule interactions. We find that PBEint and hPBEint (with 16.67% Hartree-Fock exchange) yield the overall best performance, working well for most of the considered properties and systems and showing a balanced behavior for different problems. In particular, due to their well-balanced accuracy, they perform well for the description of hybrid metal-molecule interfaces.

physics.chem-ph↗

Position-dependent exact-exchange energy for slabs and semi-infinite jellium

The position-dependent exact-exchange energy per particle $\varepsilon_x(z)$ (defined as the interaction between a given electron at $z$ and its exact-exchange hole) at metal surfaces is investigated, by using either jellium slabs or the semi-infinite (SI) jellium model. For jellium slabs, we prove analytically and numerically that in the vacuum region far away from the surface $\varepsilon_{x}^{\text{Slab}}(z \to \infty) \to - e^{2}/2z$, {\it independent} of the bulk electron density, which is exactly half the corresponding exact-exchange potential $V_{x}(z \to \infty) \to - e^2/z$ [Phys. Rev. Lett. {\bf 97}, 026802 (2006)] of density-functional theory, as occurs in the case of finite systems. The fitting of $\varepsilon_{x}^{\text{Slab}}(z)$ to a physically motivated image-like expression is feasible, but the resulting location of the image plane shows strong finite-size oscillations every time a slab discrete energy level becomes occupied. For a semi-infinite jellium, the asymptotic behavior of $\varepsilon_{x}^{\text{SI}}(z)$ is somehow different. As in the case of jellium slabs $\varepsilon_{x}^{\text{SI}}(z \to \infty)$ has an image-like behavior of the form $\propto - e^2/z$, but now with a density-dependent coefficient that in general differs from the slab universal coefficient 1/2. Our numerical estimates for this coefficient agree with two previous analytical estimates for the same. For an arbitrary finite thickness of a jellium slab, we find that the asymptotic limits of $\varepsilon_{x}^{\text{Slab}}(z)$ and $\varepsilon_{x}^{\text{SI}}(z)$ only coincide in the low-density limit ($r_s \to \infty$), where the density-dependent coefficient of the semi-infinite jellium approaches the slab {\it universal} coefficient 1/2.

cond-mat.other↗