We study the relaxation dynamics of the one-dimensional Tomonaga-Luttinger model after an interaction quench paying particular attention to the momentum dependence of the two-particle interaction. Several potentials of different analytical form are i
nvestigated all leading to universal Luttinger liquid physics in equilibrium. The steady-state fermionic momentum distribution shows universal behavior in the sense of the Luttinger liquid phenomenology. For generic regular potentials the large time decay of the momentum distribution function towards the steady-state value is characterized by a power law with a universal exponent which only depends on the potential at zero momentum transfer. A commonly employed ad hoc procedure fails to give this exponent. Besides quenches from zero to positive interactions we also consider abrupt changes of the interaction between two arbitrary values. Additionally, we discuss the appearance of a factor of two between the steady-state momentum distribution function and the one obtained in equilibrium at equal two-particle interaction.
Motivated by recent scanning tunneling and photoemission spectroscopy measurements on self-organized gold chains on a germanium surface we reinvestigate the local single-particle spectral properties of Luttinger liquids. In the first part we use the
bosonization approach to exactly compute the local spectral function of a simplified field theoretical low-energy model and take a closer look at scaling properties as a function of the ratio of energy and temperature. Translational invariant Luttinger liquids as well as those with an open boundary (cut chain geometry) are considered. We explicitly show that the scaling functions of both setups have the same analytic form. The scaling behavior suggests a variety of consistency checks which can be performed on measured data to experimentally verify Luttinger liquid behavior. In a second part we approximately compute the local spectral function of a microscopic lattice model---the extended Hubbard model---close to an open boundary using the functional renormalization group. We show that as a function of energy and temperature it follows the field theoretical prediction in the low-energy regime and point out the importance of nonuniversal energy scales inherent to any microscopic model. The spatial dependence of this spectral function is characterized by oscillatory behavior and an envelope function which follows a power law both in accordance with the field theoretical continuum model. Interestingly, for the lattice model we find a phase shift which is proportional to the two-particle interaction and not accounted for in the standard bosonization approach to Luttinger liquids with an open boundary. We briefly comment on the effects of several one-dimensional branches cutting the Fermi energy and Rashba spin-orbit interaction.
We address the question whether observables of an exactly solvable model of electrons coupled to (optical) phonons relax into large time stationary state values and investigate if the asymptotic expectation values can be computed using a stationary d
ensity matrix. Two initial nonequilibrium situations are considered. A sudden quench of the electron-phonon coupling, starting from the noninteracting canonical equilibrium at temperature T in the electron as well as in the phonon subsystems, leads to a rather simple dynamics. A richer time evolution emerges if the initial state is taken as the product of the phonon vacuum and the filled Fermi sea supplemented by a highly excited additional electron. Our model has a natural set of constants of motion, with as many elements as degrees of freedom. In accordance with earlier studies of such type of models we find that expectation values which become stationary can be described by the density matrix of a generalized Gibbs ensemble which differs from that of a canonical ensemble. For the model at hand it appears to be evident that the eigenmode occupancy operators should be used in the construction of the stationary density matrix.
We use Wilsons weak coupling ``momentum shell renormalization group method to show that two-particle interaction terms commonly neglected in bosonization of one-dimensional correlated electron systems with open boundaries are indeed irrelevant in the
renormalization group sense. Our study provides a more solid ground for many investigations of Luttinger liquids with open boundaries.
We compare two fermionic renormalization group methods which have been used to investigate the electronic transport properties of one-dimensional metals with two-particle interaction (Luttinger liquids) and local inhomogeneities. The first one is a p
oor mans method setup to resum ``leading-log divergences of the effective transmission at the Fermi momentum. Generically the resulting equations can be solved analytically. The second approach is based on the functional renormalization group method and leads to a set of differential equations which can only for certain setups and in limiting cases be solved analytically, while in general it must be integrated numerically. Both methods are claimed to be applicable for inhomogeneities of arbitrary strength and to capture effects of the two-particle interaction, such as interaction dependent exponents, up to leading order. We critically review this for the simplest case of a single impurity. While on first glance the poor mans approach seems to describe the crossover from the ``perfect to the ``open chain fixed point we collect evidence that difficulties may arise close to the ``perfect chain fixed point. Due to a subtle relation between the scaling dimensions of the two fixed points this becomes apparent only in a detailed analysis. In the functional renormalization group method the coupling of the different scattering channels is kept which leads to a better description of the underlying physics.
