Nonequilibrium calculations in the presence of an electric field are usually performed in a gauge, and need to be transformed to reveal the gauge-invariant observables. In this work, we discuss the issue of gauge invariance in the context of time-res
olved angle-resolved pump/probe photoemission. If the probe is applied while the pump is still on, one must ensure that the calculations of the observed photocurrent are gauge invariant. We also discuss the requirement of the photoemission signal to be positive and the relationship of this constraint to gauge invariance. We end by discussing some technical details related to the perturbative derivation of the photoemission spectra, which involve processes where the pump pulse photoexcites electrons due to nonequilibrium effects.
Bad metals have a large linear resistivity at high-T that is universally seen in oxides close to the Mott-Hubbard insulating phase. They also have an universal thermopower alpha(T): (i) at very low doping (lightly doped) alpha(T) has a pronounced low
-T peak that shifts to higher-T with doping; (ii) at moderate doping (underdoped) alpha(T) has a small low-T peak that shifts to lower-T with doping and has a high-T sign change; and (iii) at the highest doping (overdoped) alpha(T) is negative and depends monotonically on T. Here we show that the simplified Hubbard model provides an easy to understand description of this phenomena due to the universal form for the chemical potential versus T for doped Mott insulators and the applicability of the Kelvin formula for the thermopower.
Using inhomogeneous dynamical mean-field theory, we argue that the normal-metal proximity effect forces any finite number of barrier planes that are described by the (paramagnetic) Hubbard model and sandwiched between semi-infinite metallic leads to
always be a Fermi liquid at T=0. This then implies that the inhomogeneous system restores lattice periodicity at zero frequency, has a well-defined Fermi surface, and should display perfect (ballistic) conductivity or transparency. These results are, however, fragile with respect to finite frequency, V, T, disorder, or magnetism, all of which restore the expected quantum tunneling regime through a finite-width Mott insulator. Our formal results are complemented by numerical renormalization group studies on small thickness barriers that illustrate under what circumstances this behavior might be seen in real experimental systems.
The formalism for exactly calculating the retarded and advanced Greens functions of strongly correlated lattice models in a uniform electric field is derived within dynamical mean-field theory. To illustrate the method, we solve for the nonequilibriu
m density of states of the Hubbard model in both the metallic and Mott insulating phases at half-filling (with an arbitrary strength electric field) by employing the numerical renormalization group as the impurity solver. This general approach can be applied to any strongly correlated lattice model in the limit of large dimensions.
Regular pattern formation is ubiquitous in nature; it occurs in biological, physical, and materials science systems. Here we propose a set of experiments with ultracold atoms that show how to examine different types of pattern formation. In particula
r, we show how one can see the analog of labyrinthine patterns (so-called quantum emulsions) in mixtures of light and heavy atoms (that tend to phase separate) by tuning the trap potential and we show how complex geometrically ordered patterns emerge (when the mixtures do not phase separate), which could be employed for low-temperature thermometry. The complex physical mechanisms for the pattern formation at zero temperature are understood within a theoretical analysis called the local density approximation.
