arXiv subjects

Ion Mitxelena

Publications and source records attributed to Ion Mitxelena.

13 recordsLinked to original sources

arXiv2026

5- and 6-membered rings: A natural orbital functional study

The Global Natural Orbital Functional (GNOF) provides a straightforward approach to capture most electron correlation effects without needing perturbative corrections or limited active spaces selection. In this work, we evaluate both the original GNOF and its modified variant GNOFm on a set of twelve 5- and 6-membered molecular rings, systems characterized primarily by dynamic correlation. This reference set is vital as it comprises essential substructures of more complex molecules. We report complete-basis-set limit correlation energies for GNOF, GNOFm, and the benchmark CCSD(T) method. Across the Dunning basis sets, both functionals deliver a balanced and accurate description of the molecular set, with GNOFm showing small but systematic improvements while preserving the overall robustness of the original formulation. These results confirm the reliability of the GNOF family and its ability to capture dynamic correlation effects.

physics.chem-ph↗

arXiv2025

DoNOF 2.0: A modern Open-Source Electronic Structure Program for Natural Orbital Functionals

In this work, we present the second version of the Donostia Natural Orbital Functional Software, an open-source program for natural orbital functional calculations. The new release incorporates improved optimization algorithms, capabilities for excited-state computations, support for ab initio molecular dynamics, and integration with the libcint library. DoNOF 2.0 also extends its property toolbox by enabling the evaluation of nonlinear optical responses, including static polarizabilities and higher-order hyperpolarizabilities via a finite-field Romberg-Richardson scheme. Program Summary [Title: DoNOF; Developer's repository link: http://github.com/DoNOF/; Program's Manual link: https://donof.readthedocs.io/; Licensing provisions: GPLv3; Programming language: Fortran; additional implementations available in Python (PyNOF) and Julia (DoNOF.jl); Multinode capability: Support for distributed execution through a hybrid OpenMPI and OpenMP implementation]

physics.chem-ph↗

arXiv2024

Assessing the Global Natural Orbital Functional Approximation on Model Systems with Strong Correlation

In the past decade, natural orbital functional (NOF) approximations have emerged as prominent tools for characterizing electron correlation. Despite their effectiveness, these approaches, which rely on natural orbitals and their associated occupation numbers, often require hybridization with other methods to fully account for all correlation effects. Recently, a global NOF (GNOF) has been proposed [Phys. Rev. Lett. 127, 233001 (2021)] to comprehensively address both dynamic and static correlations. This study evaluates the performance of GNOF on strongly correlated model systems, including comparisons with highly accurate Full Configuration Interaction (FCI) calculations for hydrogen atom clusters in one, two, and three dimensions. Additionally, the investigation extends to a BeH2 reaction, involving the insertion of a beryllium atom into a hydrogen molecule along a C2v pathway. According to the results obtained using GNOF, consistent behavior is observed across various correlation regions, encompassing a range of occupation and orbital schemes. Furthermore, distinctive features are identified when varying the dimensionality of the system.

physics.chem-ph↗

arXiv2022

Benchmarking GNOF against FCI in challenging systems in one, two and three dimensions

This work assess the reliability of the recently proposed [Phys. Rev. Lett. 127, 233001, 2021] global natural orbital functional (GNOF) in the treatment of the strong electron correlation regime. We first use an H10 benchmark set of four hydrogen model systems of different dimensionalities and distinctive electronic structures: a 1D chain, a 2D ring, a 2D sheet, and a 3D close-packed pyramid. Second, we study two paradigmatic models for strongly correlated Mott insulators, namely a 1D H50 chain and a 4x4x4 3D H cube. We show that GNOF without hybridization to other electronic structure methods and free of tuned parameters succeeds in treating weak and strong correlation in a more balanced way than the functionals that have preceded it.

physics.chem-ph↗

arXiv2020

DoNOF: an open-source implementation of natural-orbital-functional-based methods for quantum chemistry

The natural orbital functional theory (NOFT) has emerged as an alternative formalism to both density functional (DF) and wavefunction methods. In NOFT, the electronic structure is described in terms of the natural orbitals (NOs) and their occupation numbers (ONs). The approximate NOFs have proven to be more accurate than those of the density for systems with a significant multiconfigurational character, on one side, and scale better with the number of basis functions than correlated wavefunction methods, on the other side. A challenging task in NOFT is to efficiently perform orbital optimization. In this article we present DoNOF, our open source implementation based on diagonalizations that allows to obtain the resulting orbitals automatically orthogonal. The one-particle reduced-density matrix (1RDM) of the ensemble of pure-spin states provides the proper description of spin multiplets. The capabilities of the code are tested on the water molecule, namely, geometry optimization, natural and canonical representations of molecular orbitals, ionization potential, and electric moments. In DoNOF, the electron-pair-based NOFs developed in our group PNOF5, PNOF7 and PNOF7s are implemented. These JKL-only NOFs take into account most non-dynamic effects plus intrapair-dynamic electron correlation, but lack a significant part of interpair-dynamic correlation. Correlation corrections are estimated by the single-reference NOF-MP2 method that simultaneously calculates static and dynamic electron correlations taking as a reference the Slater determinant formed with the NOs of a previous PNOF calculation. The NOF-MP2 method is used to analyze the potential energy surface (PES) and the binding energy for the symmetric dissociation of the water molecule, and compare it with accurate wavefunction-based methods.

physics.comp-ph↗

arXiv2020

Analytic gradients for spin multiplets in natural orbital functional theory

Analytic energy gradients with respect to nuclear motion are derived for non-singlet compounds in the natural orbital functional theory. We exploit the formulation for multiplets in order to obtain a simple formula valid for any many-electron system in its ground mixed state with a total spin S and all possible spin projection Sz values. We demonstrate that the analytic gradients can be obtained without resorting to linear response theory or involving iterative procedures. It is required a single evaluation, so integral derivatives can be computed on-the-fly along the calculation and thus improve the effectiveness of screening by the Schwarz inequality. Results for small and medium size molecules with many spin multiplicities are shown. Our results are compared with experimental data and accurate theoretical equilibrium geometries.

physics.chem-ph↗

arXiv2020

An efficient method for strongly correlated electrons in two-dimensions

This work deals with the problem of strongly correlated electrons in two-dimensions (2D). We give a reduced density matrix (RDM) based tool through which the ground-state energy is given as a functional of the natural orbitals and their occupation numbers. Specifically, the Piris Natural Orbital Functional 7 (PNOF7) is used for studying the 2D Hubbard model and hydrogen square lattices. The singlet ground-state is studied, as well as the doublet mixed quantum state obtained by extracting an electron from the system. Our method satisfies two-index necessary N-representability conditions of the two-particle RDM (2RDM) and guarantees the conservation of the total spin. We show the ability of PNOF7 to describe strong correlation effects in these 2D systems by comparing our results with exact diagonalization, density matrix renormalization group (DMRG), and auxiliary-field quantum Monte Carlo calculations. PNOF7 overcomes variational 2RDM methods with two- and three-index positivity N-representability conditions, reducing computational cost to mean-field scaling. Consistent results are obtained for small and large systems up to 144 electrons, weak and strong correlation regimes, and many filling situations. Unlike other methods, there is no dependence on dimensionality in the results obtained with PNOF7, and no particular difficulties have been observed to converge PNOF7 away from half-filling. Smooth double occupancy of sites is obtained regardless of the filling. Symmetric dissociation of 2D hydrogen lattices shows that long-range nondynamic correlation drammatically affects electron detachment energies. PNOF7 compares well with DMRG along the dissociation curve.

cond-mat.str-el↗

arXiv2019

An efficient method for strongly correlated electrons in one dimension

The one-particle reduced density matrix functional theory in its natural orbital functional (NOF) version is used to study strongly correlated electrons. We show the ability of the Piris NOF 7 (PNOF7) to describe non-dynamic correlation effects in one-dimensional (1D) systems. An extensive study of 1D systems that includes Hydrogen (H) chains and the 1D Hubbard model with periodic boundary conditions is provided. Different filling situations and large sizes with up to 122 electrons are considered. Compared to quasi-exact results, PNOF7 is accurate in different correlation regimes for the 1D Hubbard model even away from the half-filling, and maintains its accuracy when the system size increases. The symmetric and asymmetric dissociations of the linear H chain composed of 50 atoms are described to remark the importance of long-range interactions in presence of strong correlation effects. Our results compare remarkably well with those obtained at the density-matrix renormalization group level of theory.

cond-mat.str-el↗

arXiv2019

Natural orbital functional for spin-polarized periodic systems

Natural orbital functional theory is considered for systems with one or more unpaired electrons. An extension of the Piris natural orbital functional (PNOF) based on electron pairing approach is presented, specifically, we extend the independent pair model, PNOF5, and the interactive pair model PNOF7 to describe spin-uncompensated systems. An explicit form for the two-electron cumulant of high-spin cases is only taken into account, so that singly occupied orbitals with the same spin are solely considered. The rest of electron pairs with opposite spins remain paired. The reconstructed two-particle reduced density matrix fulfills certain N-representability necessary conditions, as well as guarantees the conservation of the total spin. The theory is applied to model systems with strong non-dynamic (static) electron correlation, namely, the one-dimensional Hubbard model with periodic boundary conditions and hydrogen rings. For the latter, PNOF7 compares well with exact diagonalization results so the model presented here is able to provide a correct description of the strong-correlation effects.

physics.chem-ph↗

arXiv2018

Phase Dilemma in Natural Orbital Functional Theory from the N-representability Perspective

Any rigorous approach to first-order reduced density (1RDM) matrix functional theory faces the phase dilemma, that is, having to deal with a large number of possible combinations of signs in terms of the electron-electron interaction energy. This problem was discovered by reducing a ground-state energy generated from an approximate N-particle wavefunction into a functional of the 1RDM, known as the top-down method. Here, we show that the phase dilemma also appears in the bottom-up method, in which the functional E[1RDM] is generated by progressive inclusion of N-representability conditions on the reconstructed two-particle reduced density matrix. It is shown that an adequate choice of signs is essential to accurately describe model systems with strong non-dynamic (static) electron correlation, specifically, the one-dimensional Hubbard model with periodic boundary conditions and hydrogen rings. For the latter, the Piris natural orbital functional 7 (PNOF7), with phases equal to -1 for the inter-pair energy terms containing the exchange-time-inversion integrals, agrees with exact diagonalization results.

physics.chem-ph↗

arXiv2018

Analytic second-order energy derivatives in natural orbital functional theory

The analytic energy gradients in the atomic orbital representation have recently been published (J. Chem. Phys. 146, 014102, 2017) within the framework of the natural orbital functional theory (NOFT). We provide here an alternative expression for them in terms of natural orbitals, and use it to derive the analytic second-order energy derivatives with respect to nuclear displacements in the NOFT. The computational burden is shifted to the calculation of perturbed natural orbitals and occupancies, since a set of linear coupled-perturbed equations obtained from the variational Euler equations must be solved to attain the analytic Hessian at the perturbed geometry. The linear response of both natural orbitals and occupation numbers to nuclear geometry displacements need only specify the reconstruction of the second-order reduced density matrix in terms of occupation numbers.

physics.chem-ph↗

arXiv2016

Analytic gradients for natural orbital functional theory

The analytic energy gradients with respect to nuclear motion are derived for natural orbital functional (NOF) theory. The resulting equations do not require to resort to linear-response theory, so the computation of NOF energy gradients is analogous to gradient calculations at the Hartree-Fock level of theory. The structures of 15 spin-compensated systems, composed by first- and second-row atoms, are optimized employing the conjugate gradient algorithm. As functionals, two orbital-pairing approaches were used, namely, the fifth and sixth Piris NOFs (PNOF5 and PNOF6). For the latter, the obtained equilibrium geometries are compared with coupled cluster singles and doubles (CCSD) calculations and accurate empirical data.

physics.chem-ph↗

arXiv2016

Molecular electric moments calculated by using natural orbital functional theory

The molecular electric dipole, quadrupole and octupole moments of a selected set of 21 spin-compensated molecules are determined employing the extended version of the Piris natural orbital functional 6 (PNOF6), using the triple-$ζ$ Gaussian basis set with polarization functions developed by Sadlej, at the experimental geometries. The performance of the PNOF6 is established by carrying out a statistical analysis of the mean absolute errors with respect to the experiment. The calculated PNOF6 electric moments agree satisfactorily with the corresponding experimental data, and are in good agreement with the values obtained by accurate ab initio methods, namely, the coupled-cluster single and doubles (CCSD) and multi-reference single and double excitation configuration interaction (MRSD-CI) methods.

physics.chem-ph↗