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Matthias Ernzerhof

Publications and source records attributed to Matthias Ernzerhof.

4 recordsLinked to original sources

The uncharted space of non-Hermitian solutions to the Hartree-Fock and Kohn-Sham equations

Many problems in physical chemistry involve systems that are coupled to an environment, such as a molecule interacting with an adjacent surface, possibly resulting in meta-stable molecular states where electron density is transferred to the surface. Such systems can be described by non-Hermitian quantum mechanics (NHQM), where the Hamiltonian includes dissipative terms. Within NHQM, one can also formulate the Hartree-Fock (HF) and Kohn-Sham (KS) methods and, as in the conventional theory, an effective independent-particle picture is employed. The crucial observation of the present work is that even for systems that are not coupled to an environment, in the HF or KS equation a single electron is coupled to a bath of the remaining electrons which can act as an environment, opening up the possibility for the exchange of current density between the one-electron and the remaining N-1 electron system. The corresponding self-consistent states represent a new uncharted space of solutions to the HF and KS equations. We show that the additional solutions can have a physical interpretation and thus extend the range of problems HF and KS can be applied to. If open-system HF and KS calculations are performed, the new class of solutions is always encountered but this has also not been noted previously.

quant-ph

Peierls Instability in Carbon Nanotubes

We present a first-principles study of Peierls distortions in \emph{trans}-polyacetylene, polyacene, and armchair $(n,n)$ carbon nanotubes. Our findings suggest that the ground-state geometries of armchair $(n,n)$ carbon nanotubes, with $n$ up to 6, exhibit a Peierls distortion as it is found for \emph{trans}-polyactetylene. In contrast to previous studies in which no Peierls distortion is found with conventional local and semi-local density functionals, we use a hybrid functional whose exact-exchange admixture has been specifically optimized for the problem at hand.

cond-mat.mtrl-sci

Strong correlation effects in diatomic molecular electronic devices

We present a qualitative model for a fundamental process in molecular electronics: the change in conductance upon bond breaking. In our model a diatomic molecule is attached to spin-polarized contacts. Employing a Hubbard Hamiltonian, electron interaction is neglected in the contacts and explicitly considered in the molecule, enabling us to study the impact of electron interaction on the molecular conductance. In the limit where the electron repulsion is strong compared to the binding energy (as it becomes the case upon dissociation) electron transmission in strongly suppressed compared to the non-interacting case. However, the spin-polarized nature of the contacts introduces a coupling between the molecular singlet and triplet states. This coupling in turn yields additional resonances in the transmission probability that significantly reduce the energetic separation appear between resonances. The ramifications of our results on transport experiments performed on nanowires with inclusions $H_2$ are discussed.

cond-mat.mtrl-sci

Ab initio study of ladder-type polymers polythiophene and polypyrrole

This article presents an \textit{ab initio} study of four polymers, polythiophene, polypyrrole, ladder-type polythiophene, and ladder-type polypyrrole. Upon an analysis of the variation of the band gap when comparing the unconstrained and the ladder-type polymers, a discrepancy was found between the thiophene and the pyrrole polymer families. For polythiophene, the ladder-type polymer has a larger gap than the unconstrained polymer whereas the opposite is found for the pyrrole polymers. The structural properties and the charge densities using the Bader charge analysis of these four compounds are investigated. The different band gap behaviors in thiophene and pyrrole polymers can be explained in terms of the competition between the bond length alternation and the effect of the charge density in the carbon backbone.

cond-mat.mtrl-sci