arXiv subjects

Simon Liebing

Publications and source records attributed to Simon Liebing.

7 recordsLinked to original sources

arXiv2022

Effect of color superconductivity on the mass of hybrid neutron stars in an effective model with pQCD asymptotics

The effective cold quark matter model by Alford, Braby, Paris and Reddy (ABPR) is used as a tool for discussing the effect of the size of the pairing gap in three-flavor (CFL) quark matter on the maximum mass of hybrid neutron stars (NSs). This equation of state (EOS) has three parameters which we suggest to determine by comparison with a nonlocal NJL model of quark matter in the nonperturbative domain. We show that due to the momentum dependence of the pairing which is induced by the nonlocality of the interaction, the effective gap parameter in the EOS model is well approximated by a constant value depending on the diquark coupling strength in the NJL model Lagrangian. For the parameter $a_4=1-2\alpha_s/\pi$ a constant value below about \num{0.4} is needed to explain hybrid stars with ${\rm M}_{\rm max} \gtrsim 2.0~{\rm M}_\odot$, which would translate to an effective constant $\alpha_s\sim 1$. The matching point with a running coupling at the 1-loop $\beta$ function level is found to lie outside the range of chemical potentials accessible in NS interiors. A dictionary is provided for translating the free parameters of the nlNJL model to those of the ABPR model. Both models are shown to be equivalent in the nonperturbative domain but the latter one allows to quantify the transition to the asymptotic behaviour in accordance with perturbative QCD. We provide constraints on parameter sets that fulfill the $2~{\rm M}_\odot$ mass constraint for hybrid NSs, as well as the low tidal deformability constraint from GW170817 by a softening of the EOS on the hybrid NS branch with an early onset of deconfinement at ${\rm M}_{\rm onset}<1.4~{\rm M}_\odot$. We find that the effective constant pairing gap should be around 100 MeV but not exceed values of about 130 MeV because a further increase of the gap would entail a softening of the EOS and contradict the $2~{\rm M}_\odot$ mass constraint.

nucl-th↗

arXiv2022

Effect of molecular and electronic geometries on the electronic density in FLO-SIC

Recently, Trepte et al. [J. Chem. Phys., vol. 155, 2021] pointed out the importance of analyzing dipole moments in the Fermi-L\"owdin orbital (FLO) self-interaction correction (SIC) for cyclic, planar molecules. In this manuscript, the effect of the molecular and electronic geometries on dipole moments and polarizabilities is discussed for non-cyclic molecules. Computed values are presented for water, formaldehyde, and nitromethane. Continuing the work of Schwalbe et al. [J. Chem. Phys. vol. 153, (2020)], we reconfirm that systematic numerical parameter studies are essential to obtain consistent results in density functional theory (DFT) and SIC. In agreement with Trepte et al. [J. Chem. Phys., vol. 155, 2021], DFT agrees well with experiment for dipole moments, while SIC slightly overestimates them. A Linnett double-quartet electronic geometry is found to be energetically preferred for nitromethane.

physics.chem-ph↗

arXiv2021

Chemical bonding theories as guides for self-interaction corrected solutions: multiple local minima and symmetry breaking

Fermi--L\"owdin orbitals (FLO) are a special set of localized orbitals, which have become commonly used in combination with the Perdew--Zunger self-interaction correction (SIC) in the FLO-SIC method. The FLOs are obtained for a set of occupied orbitals by specifying a classical position for each electron. These positions are known as Fermi-orbital descriptors (FODs), and they have a clear relation to chemical bonding. In this study, we show how FLOs and FODs can be used to initialize, interpret and justify SIC solutions in a common chemical picture, both within FLO-SIC and in traditional variational SIC, and to locate distinct local minima in either of these approaches. We demonstrate that FLOs based on Lewis' theory lead to symmetry breaking for benzene -- the electron density is found to break symmetry already at the symmetric molecular structure -- while ones from Linnett's double-quartet theory reproduce symmetric electron densities and molecular geometries. Introducing a benchmark set of 16 planar, cyclic molecules, we show that using Lewis' theory as the starting point can lead to artifactual dipole moments of up to 1 Debye, while Linnett SIC dipole moments are in better agreement with experimental values. We suggest using the dipole moment as a diagnostic of symmetry breaking in SIC and monitoring it in all SIC calculations. We show that Linnett structures can often be seen as superpositions of Lewis structures and propose Linnett structures as a simple way to describe aromatic systems in SIC with reduced symmetry breaking. The role of hovering FODs is also briefly discussed.

physics.comp-ph↗

arXiv2019

Electronic structure and transport properties of coupled CdS/ZnSe quantum dots

Electronic structure and transport characteristics of coupled CdS and ZnSe quantum dots are studied using density functional theory and non equilibrium Greens function method respectively. Our investigations show that in these novel coupled dots, the frontier occupied and unoccupied molecular orbitals are spatially located in two different parts of the coupled dot, thereby indicating the possibility of asymmetry in electronic transport. We have calculated electronic transport through the coupled quantum dot by varying the coupling strength between the individual quantum dots in the limits of weak and strong coupling. Calculations reveal asymmetric current vs voltage curves in both the limits indicating the rectifying properties of the coupled quantum dots. Additionally we discuss the possibility to tune the switching behavior of the coupled dots by different gate geometries.

cond-mat.mes-hall↗

arXiv2015

Fermi orbital self-interaction corrected electronic structure of molecules beyond local density approximation

The correction of the self-interaction error (SIE) that is inherent to all standard density functional theory (DFT) calculations is an object of increasing interest. In this article we apply the very recently developed Fermi-orbital based approach for the self-interaction correction (FOSIC) to a set of different molecular systems. Our study covers systems ranging from simple diatomic to large organic molecules. We focus our analysis on the direct estimation of the ionization potential from orbital eigenvalues.

physics.comp-ph↗

arXiv2014

Electronic and magnetic properties of Co_n Mo_m nanoclusters with n+m = x and 2<=x<=6 atoms from DFT calculations

We present the results of the density functional theory study of Co_n Mo_m nanoclusters with n+m=x and 2<=x<=6 atoms on the all-electron level using the generalized gradient approximation. The discussion of the properties of the pure cobalt and molybdenium cluster is followed by an analysis of the respective mixed clusters of each cluster size x. We found that the magnetic moment of a given cluster is mainly due to the Co content and increases with increasing n. The magnetic anisotropy on the other hand becomes smaller for larger magnetic moments S. We observe an increase in the binding energy, electron affinity, and average bond length with increasing cluster size as well as a decrease in the ionization potential, chemical potential, molecular hardness and the HOMO-LUMO gap.

cond-mat.mes-hall↗

arXiv2014

Gate Controlled Molecular Switch Based on Picene/F4TCNQ Charge-Transfer Material

We show that the recently synthesized charge-transfer material picene/F4TCNQ can be used as a gate-voltage controlled molecular switch. The picene/F4TCNQ system is compared with the extensive characterized anthraquinone-based molecular system, which is known to exhibit large switching ratios due to quantum interference effects. In case of picene/F4TCNQ we find switching ratios larger by one order of magnitude. Further, our calculations reveal that the picene/F4TCNQ system resembles remarkable well the I-V characteristics of a classical diode. The reverse-bias current of this molecular diode can be increased two orders of magnitude by an external gate voltage. Based on density-functional theory calculations we show that the hybrid states formed by the picene/F4TCNQ system are playing the key role to determine the transport properties. We further conclude that the tuning of quantum transport properties through hybrid states is a general concept which opens a new route towards functional materials for molecular electronics.

cond-mat.mes-hall↗