The spin-dependent Falicov-Kimball model (FKM) is studied on a triangular lattice using numerical diagonalization technique and Monte-Carlo simulation algorithm. Magnetic properties have been explored for different values of parameters: on-site Coulo
mb correlation $U$, exchange interaction $J$ and filling of electrons. We have found that the ground state configurations exhibit long range Ne`el order, ferromagnetism or a mixture of both as $J$ is varied. The magnetic moments of itinerant ($d$) and localized ($f$) electrons are also studied. For the one-fourth filling case we found no magnetic moment from $d$- and $f$-electrons for $U$ less than a critical value.
A numerical diagonalization technique with canonical Monte-Carlo simulation algorithm is used to study the phase transitions from low temperature (ordered) phase to high temperature (disordered) phase of spinless Falicov-Kimball model on a triangular
lattice with correlated hopping ($t^{prime}$). It is observed that the low temperature ordered phases (i.e. regular, bounded and segregated) persist up to a finite critical temperature ($T_{c}$). In addition, we observe that the critical temperature decreases with increasing the correlated hopping in regular and bounded phases whereas it increases in the segregated phase. Single and multi peak patterns seen in the temperature dependence of specific heat ($C_v$) and charge susceptibility ($chi$) for different values of parameters like on-site Coulomb correlation strength ($U$), correlated hopping ($t^{prime}$) and filling of localized electrons ($n_{f}$) are also discussed.
Thermodynamic properties of the spinless Falicov-Kimball model are studied on a triangular lattice using numerical diagonalization technique with Monte-Carlo simulation algorithm. Discontinuous metal-insulator transition is observed at finite tempera
ture. Unlike the case of square lattice, here we observe that the finite temperature effect is not able to smear out the discontinuous metal-insulator transition seen in the ground state. Calculation of specific heat (C_v) shows single and double peak structures for different values of parameters like on-site correlation strength (U), f-electron energy (E_f) and temperature.
A two-electron one-dimensional model of a heteroatomic molecule composed of two open-shell atoms is considered. Including only two electrons isolates and examines the effect that the highest occupied molecular orbital has on the Kohn-Sham potential a
s the molecule dissociates. We reproduce the characteristic step and peak that previous high-level wavefunction methods have shown to exist for real molecules in the low-density internuclear region. The simplicity of our model enables us to investigate in detail their development as a function of bond-length, with little computational effort, and derive properties of their features in the dissociation limit. We show that the onset of the step is coincident with the internuclear separation at which an avoided crossing between the ground-state and lowest charge-transfer excited state is approached. Although the step and peak features have little effect on the ground-state energetics, we discuss their important consequences for dynamics and response.
A recent paper (Phys. Rev A. 75, 022513 (2007), arXiv:cond-mat/0602020) challenges exact time-dependent density functional theory (TDDFT) on several grounds. We explain why these criticisms are either irrelevant or incorrect, and that TDDFT is both formally exact and predictive.
Systems whose underlying classical dynamics are chaotic exhibit signatures of the chaos in their quantum mechanics. We investigate the possibility of using time-dependent density functional theory (TDDFT) to study the case when chaos is induced by el
ectron-interaction alone. Nearest-neighbour level-spacing statistics are in principle exactly and directly accessible from TDDFT. We discuss how the TDDFT linear response procedure can reveal the mechanism of chaos induced by electron-interaction alone. A simple model of a two-electron quantum dot highlights the necessity to go beyond the adiabatic approximation in TDDFT.
We discuss the relationship between modern time-dependent density functional theory and earlier time-period
