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Matthias Ernzerhof

Publications and source records attributed to Matthias Ernzerhof.

5 recordsLinked to original sources

Density functional theory of complex transition densities.

We present an extension of Hohenberg-Kohn-Sham density functional theory to the domain of complex local potentials and complex electron densities. The approach is applicable to resonance (Siegert) [Phys. Rev. 56, 750 (1939)] states and other scattering and transport problems that can be described by a normalized state of a Hamiltonian containing a complex local potential. Such Hamiltonians are non-Hermitian and their eigenvalues are in general complex, the imaginary part being inversely proportional to the lifetime of the system. The one-to-one correspondence between complex local potentials nu and complex electron densities rho is established provided that the complex variables are sufficiently close to real local potentials and densities of nondegenerate ground states. We show that the exchange-correlation functionals, contributing to the complex energy, are determined through analytic continuation of their ground-state-theory counterparts. This implies that the exchange-correlation effects on the lifetime of a resonance are, under appropriate conditions, already determined by the functionals of the ground-state theory.

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Side-chain effects in molecular electronic devices.

We discuss the effect of an abundant structural element of molecules on the transmission probabilities of molecular electronic devices. We show that an attachment of side chains to a molecular conductor may lead to zero transmission probabilities. The gaps in the transmission-probability appear approximately at the eigenvalues of the isolated side chains, provided that the corresponding eigenstates are not localized away from the molecular conductor. Simple Hückel-type calculations serve to illustrate the described effect. Furthermore, we show that complex transmission-probability curves, obtained with Kohn-Sham density-functional theory, also exhibit the described side-chain effect.

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Approximate density functionals applied to molecular quantum dots.

Recently, molecular quantum dots (MQDs) have been investigated experimentally and found to exhibit the Kondo effect. The Kondo effect leads to an enhancement of the zero-voltage conductance. Here, we study a finite cluster model of a MQD by means of Kohn-Sham density functional theory. Furthermore, employing an implementation of Landauer's formula, we calculate the conductance of the dot. We find that the electronic structure and the molecular conductance depend strongly on the exchange-correlation functional employed. While the local spin density approximation and the Perdew-Burke-Ernzerhof (PBE) generalized gradient approximation qualitatively reproduce certain features of the Kondo effect, PBE hybrid does not. Based on the MQD, we discuss the limitations of using density functional theory to model molecular electronic devices.

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Zero-voltage conductance of short gold nanowires.

Using the Landauer formula, the conductance of short gold wires is studied. The required electronic structure calculations are performed with a self-consistent tight-binding method. We consider gold wires of single-atom diameter with a variable number (N=1, em leader,5) of atoms. Depending on N, we find considerable conductance variations with one conductance quantum being the upper limit. The results are confirmed by means of Friedel's sum rule. Tip-shaped clusters are used to provide the contact-wire interfaces and the relation between various tip structures and the conductance is discussed. Our predictions about the conductance variations agree qualitatively with new experimental results.

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Current-dependent extension of the Perdew-Burke-Ernzerhof exchange-correlation functional.

The probability current density is used in addition to the electron density and its gradient as a variable in the construction of an exchange-correlation functional. Starting from the Perdew-Burke-Ernzerhof generalized gradient approximation, we employ exact conditions to build a nonempirical exchange functional. Matching the correlation functional to that for exchange yields a current-dependent approximation for correlation. The resulting functional is given in a simple closed form. Application of this approximation to open shell atoms eliminates the artificial level splitting of formally degenerate states observed with generalized gradient approximations.

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