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Register a new userDissipation-assisted operator evolution method for capturing hydrodynamic transport
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We introduce the dissipation-assisted operator evolution (DAOE) method for calculating transport properties of strongly interacting lattice systems in the high temperature regime. DAOE is based on evolving observables in the Heisenberg picture, and applying an artificial dissipation that reduces the weight on non-local operators. We represent the observable as a matrix product operator, and show that the dissipation leads to a decay of operator entanglement, allowing us to capture the dynamics to long times. We test this scheme by calculating spin and energy diffusion constants in a variety of physical models. By gradually weakening the dissipation, we are able to consistently extrapolate our results to the case of zero dissipation, thus estimating the physical diffusion constant with high precision.
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We present a new framework for computing low frequency transport properties of strongly correlated, ergodic systems. Our main assumption is that, when a thermalizing diffusive system is driven at frequency $omega$, domains of size $xi simsqrt{D/omega}$ can be considered as internally thermal, but weakly coupled with each other. We calculate the transport coefficients to lowest order in the coupling, assuming incoherent transport between such domains. Our framework naturally captures the sub-leading non analytic corrections to the transport coefficients, known as hydrodynamic long time tails. In addition, it allows us to obtain a generalized relation between charge and thermal transport coefficients, in the spirit of the Wiedemann-Franz law. We verify our results, which satisfy several non-trivial consistency checks, via exact diagonalization studies on the one-dimensional extended Fermi-Hubbard model.
Materials with strongly-correlated electrons exhibit interesting phenomena such as metal-insulator transitions and high-temperature superconductivity. In stark contrast to ordinary metals, electron transport in these materials is thought to resemble the flow of viscous fluids. Despite their differences, it is predicted that transport in both, conventional and correlated materials, is fundamentally limited by the uncertainty principle applied to energy dissipation. Here we discover hydrodynamic electron flow in the Weyl-semimetal tungsten phosphide (WP2). Using thermal and magneto-electric transport experiments, we observe the transition from a conventional metallic state, at higher temperatures, to a hydrodynamic electron fluid below 20 K. The hydrodynamic regime is characterized by a viscosity-induced dependence of the electrical resistivity on the square of the channel width, and by the observation of a strong violation of the Wiedemann-Franz law. From magneto-hydrodynamic experiments and complementary Hall measurements, the relaxation times for momentum and thermal energy dissipating processes are extracted. Following the uncertainty principle, both are limited by the Planckian bound of dissipation, independent of the underlying transport regime.
We study hydrodynamic phonon heat transport in two-dimensional (2D) materials. Starting from the Peierls-Boltzmann equation within the Callaway model, we derive a 2D Guyer-Krumhansl-like equation describing non-local hydrodynamic phonon transport, taking into account the quadratic dispersion of flexural phonons. In additional to Poiseuille flow, second sound propagation, the equation predicts heat current vortices and negative nonlocal thermal conductance in 2D materials, common in classical fluid but scarcely considered in phonon transport. Our results also illustrate the universal transport behavior of hydrodynamics, independent on the type of quasi-particles and their microscopic interactions.
We develop a strong-disorder renormalization group to study quantum phase transitions with continuous O$(N)$ symmetry order parameters under the influence of both quenched disorder and dissipation. For Ohmic dissipation, as realized in Hertz theory of the itinerant antiferromagnetic transition or in the superconductor-metal transition in nanowires, we find the transition to be governed by an exotic infinite-randomness fixed point in the same universality class as the (dissipationless) random transverse-field Ising model. We determine the critical behavior and calculate key observables at the transition and in the associated quantum Griffiths phase. We also briefly discuss the cases of superohmic and subohmic dissipations.
Universal phenomena far from equilibrium exhibit additional independent scaling exponents and functions as compared to thermal universal behavior. For the example of an ultracold Bose gas we simulate nonequilibrium transport processes in a universal scaling regime and show how they lead to the breaking of the fluctuation-dissipation relation. As a consequence, the scaling of spectral functions (commutators) and statistical correlations (anticommutators) between different points in time and space become linearly independent with distinct dynamic scaling exponents. As a macroscopic signature of this phenomenon we identify a transport peak in the statistical two-point correlator, which is absent in the spectral function showing the quasiparticle peaks of the Bose gas.
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