arXiv subjects

Felix Hummel

Publications and source records attributed to Felix Hummel.

28 records · Page 2Linked to original sources

arXiv2019

Finite temperature coupled cluster theories for extended systems

At zero temperature coupled cluster theory is widely used to predict total energies, ground state expectation values and even excited states for molecules and extended systems. Generalizations to finite temperature exist, however, they are in practice several orders of magnitude more demanding compared to the zero temperature case since the amplitudes must be computed and stored for many Matsubara frequencies to yield sufficiently accurate results. Instead of using Matsubara frequencies one can also work directly in the imaginary time domain on the compact interval [0, beta]. The arising imaginary time dependent coupled cluster amplitude integral equations are solved numerically on a non-uniform grid. About a dozen grid points provide sufficient accuracy if the Hamiltonian is repartitioned to include particle/hole interactions in the non-perturbative part. In this framework the transition from finite to zero temperature is uniform and comes at no extra costs, allowing, for instance, to benchmark fractional occupancy formulations of coupled cluster theories. Finite temperature direct ring coupled cluster doubles free energies are calculated for various temperatures for solid lithium, a metallic system, and for solid silicon, a semiconductor.

cond-mat.mtrl-sci↗

arXiv2019

On the duality of ring and ladder diagrams and its importance for many-electron perturbation theories

We present a diagrammatic decomposition of the transition pair correlation function for the uniform electron gas. We demonstrate explicitly that ring and ladder diagrams are dual counterparts that capture significant long- and short-ranged interelectronic correlation effects, respectively. Our findings help to guide the further development of approximate many-electron theories and reveal that the contribution of the ladder diagrams to the electronic correlation energy can be approximated in an effective manner using second-order perturbation theory. We employ the latter approximation to reduce the computational cost of coupled cluster theory calculations for insulators and semiconductors by two orders of magnitude without compromising accuracy.

cond-mat.mtrl-sci↗

arXiv2018

Screened exchange corrections to the random phase approximation from many-body perturbation theory

The random phase approximation (RPA) systematically overestimates the magnitude of the correlation energy and generally underestimates cohesive energies. This originates in part from the complete lack of exchange terms, which would otherwise cancel Pauli exclusion principle violating (EPV) contributions. The uncanceled EPV contributions also manifest themselves in form of an unphysical negative pair density of spin-parallel electrons close to electron-electron coalescence. We follow considerations of many-body perturbation theory to propose an exchange correction that corrects the largest set of EPV contributions while having the lowest possible computational complexity. The proposed method exchanges adjacent particle/hole pairs in the RPA diagrams, considerably improving the pair density of spin-parallel electrons close to coalescence in the uniform electron gas (UEG). The accuracy of the correlation energy is comparable to other variants of Second Order Screened Exchange (SOSEX) corrections although it is slightly more accurate for the spin-polarized UEG. Its computational complexity scales as $\mathcal O(N^5)$ or $\mathcal O(N^4)$ in orbital space or real space, respectively. Its memory requirement scales as $\mathcal O(N^2)$.

cond-mat.mtrl-sci↗

arXiv2018

Dispersive mixed-order systems in $L^p$-Sobolev spaces and application to the thermoelastic plate equation

We study dispersive mixed-order systems of pseudodifferential operators in the setting of $L^p$-Sobolev spaces. Under the weak condition of quasi-hyperbolicity, these operators generate a semigroup in the space of tempered distributions. However, if the basic space is a tuple of $L^p$-Sobolev spaces, a strongly continuous semigroup is in many cases only generated if $p=2$ or $n=1$. The results are applied to the linear thermoelastic plate equation inertial term and with Fourier's or Maxwell-Cattaneo's law of heat conduction.

math.AP↗

arXiv2017

A comparison between quantum chemistry and quantum Monte Carlo techniques for the adsorption of water on the (001) LiH surface

We present a comprehensive benchmark study of the adsorption energy of a single water molecule on the (001) LiH surface using periodic coupled cluster and quantum Monte Carlo theories. We benchmark and compare different implementations of quantum chemical wave function based theories in order to verify the reliability of the predicted adsorption energies and the employed approximations. Furthermore we compare the predicted adsorption energies to those obtained employing widely-used van der Waals density-functionals. Our findings show that quantum chemical approaches are becoming a robust and reliable tool for condensed phase electronic structure calculations, providing an additional tool that can also help in potentially improving currently available van der Waals density-functionals.

physics.chem-ph↗

arXiv2016

Low rank factorization of the Coulomb integrals for periodic coupled cluster theory

We study the decomposition of the Coulomb integrals of periodic systems into a tensor contraction of six matrices of which only two are distinct. We find that the Coulomb integrals can be well approximated in this form already with small matrices compared to the number of real space grid points. The cost of computing the matrices scales as O(N^4) using a regularized form of the alternating least squares algorithm. The studied factorization of the Coulomb integrals can be exploited to reduce the scaling of the computational cost of expensive tensor contractions appearing in the amplitude equations of coupled cluster methods with respect to system size. We apply the developed methodologies to calculate the adsorption energy of a single water molecule on a hexagonal boron nitride monolayer in a plane wave basis set and periodic boundary conditions.

physics.chem-ph↗

arXiv2015

Hidden scale invariance of metals

Density functional theory (DFT) calculations of 58 liquid elements at their triple point show that most metals exhibit near proportionality between thermal fluctuations between virial and potential-energy in the isochoric ensemble. This demonstrates a general "hidden" scale invariance of metals making the dense part of the thermodynamic phase diagram effectively one dimensional with respect to structure and dynamics. DFT computed density scaling exponents, related to the Gr{ü}neisen parameter, are in good agreement with experimental values for 16 elements where reliable data were available. Hidden scale invariance is demonstrated in detail for magnesium by showing invariance of structure and dynamics. Computed melting curves of period three metals follow curves with invariance (isomorphs). The experimental structure factor of magnesium is predicted by assuming scale invariant inverse power-law (IPL) pair interactions. However, crystal packings of several transition metals (V, Cr, Mn, Fe, Nb, Mo, Ta, W and Hg), most post-transition metals (Ga, In, Sn, and Tl) and the metalloids Si and Ge cannot be explained by the IPL assumption. Thus, hidden scale invariance can be present even when the IPL-approximation is inadequate. The virial-energy correlation coefficient of iron and phosphorous is shown to increase at elevated pressures. Finally, we discuss how scale invariance explains the Gr{ü}neisen equation of state and a number of well-known empirical melting and freezing rules.

cond-mat.stat-mech↗

arXiv2015

Adjacent Pairs Exchange correction to the Random Phase Approximation

The Random Phase Approximation (RPA) is a widely employed post Hartree-Fock or DFT method, capable of capturing van der Waal interactions and other dynamic correlation effects at relatively low costs of $\mathcal O(N^3)$ in time and $\mathcal O(N^2)$ in memory, if calculated from imaginary time propagators. However, since it neglects anti-symmetrization RPA is biased, overestimating the correlation energy and bond lengths in general. The Second Order Screened Exchange offers amelioration by anti-symmetrizing one Coulomb interaction but it comes at considerable costs of $\mathcal O(N^5)$ in time and $\mathcal O(N^4)$ in memory, since it has to be calculated from the direct ring Coupled Cluster Doubles (drCCD) amplitudes. We propose a diagrammatic method, exchanging adjacent pairs in the RPA diagrams - hence its name - offering similar accuracy but with memory requirement of only $\mathcal O(N^2)$. The correction is calculated from imaginary time propagators similar to efficient RPA implementations. It can be calculated in $\mathcal O(N^5)$ steps in momentum space or $\mathcal O(N^4)$ steps in real space. It improves on SOSEX in the uniform electron gas for low densities, where correlation effects are stronger, and first calculations of lattice constants in solids are in excellent agreement with experiment.

cond-mat.mtrl-sci↗

arXiv2014

Computing the crystal growth rate by the interface pinning method

An essential parameter for crystal growth is the kinetic coefficient given by the proportionality between super-cooling and average growth velocity. Here we show that this coefficient can be computed in a single equilibrium simulation using the interface pinning method where two-phase configurations are stabilized by adding an spring-like bias field coupling to an order-parameter that discriminates between the two phases. Crystal growth is a Smoluchowski process and the crystal growth rate can therefore be computed from the terminal exponential relaxation of the order parameter. The approach is investigated in detail for the Lennard-Jones model. We find that the kinetic coefficient scales as the inverse square-root of temperature along the high temperature part of the melting line. The practical usability of the method is demonstrated by computing the kinetic coefficient of the elements Na, Mg, Al and Si from first principles. It is briefly discussed how a generalized version of the method is an alternative to forward flux sampling methods for computing rates along trajectories of rare events.

cond-mat.stat-mech↗

arXiv2013

Computing Gibbs free energy differences by interface pinning

We propose an approach for computing the Gibbs free energy difference between phases of a material. The method is based on the determination of the average force acting on interfaces that separate the two phases of interest. This force, which depends on the Gibbs free energy difference between the phases, is computed by applying an external harmonic field that couples to a parameter which specifies the two phases. Validated first for the Lennard-Jones model, we demonstrate the flexibility, efficiency and practical applicability of this approach by computing the melting temperatures of sodium, magnesium, aluminum and silicon at ambient pressure using density functional theory. Excellent agreement with experiment is found for all four elements, except for silicon, for which the melting temperature is, in agreement with previous simulations, seriously underestimated.

cond-mat.stat-mech↗