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Hydrodynamics is a general description for the flow of a fluid, and is expected to hold even for fundamental particles such as electrons when inter-particle interactions dominate. While various aspects of electron hydrodynamics were revealed in recent experiments, the fundamental spatial structure of hydrodynamic electrons, the Poiseuille flow profile, has remained elusive. In this work, we provide the first real-space imaging of Poiseuille flow of an electronic fluid, as well as visualization of its evolution from ballistic flow. Utilizing a scanning nanotube single electron transistor, we image the Hall voltage of electronic flow through channels of high-mobility graphene. We find that the profile of the Hall field across the channel is a key physical quantity for distinguishing ballistic from hydrodynamic flow. We image the transition from flat, ballistic field profiles at low temperature into parabolic field profiles at elevated temperatures, which is the hallmark of Poiseuille flow. The curvature of the imaged profiles is qualitatively reproduced by Boltzmann calculations, which allow us to create a phase diagram that characterizes the electron flow regimes. Our results provide long-sought, direct confirmation of Poiseuille flow in the solid state, and enable a new approach for exploring the rich physics of interacting electrons in real space.
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Hydrodynamic flow of charge carriers in graphene is an energy flow unlike the usual mass flow in conventional fluids. In neutral graphene, the energy flow is decoupled from the electric current, making it difficult to observe the hydrodynamic effects and measure the viscosity of the electronic fluid by means of electric current measurements. In particular, we show that the hallmark Poiseuille flow in a narrow channel cannot be driven by the electric field irrespective of boundary conditions at the channel edges. Nevertheless one can observe nonuniform current densities similarly to the case of the well-known ballistic-diffusive crossover. The standard diffusive behavior with the uniform current density across the channel is achieved under the assumptions of specular scattering on the channel boundaries. This flow can also be made nonuniform by applying weak magnetic fields. In this case, the curvature of the current density profile is determined by the quasiparticle recombination processes dominated by the disorder-assisted electron-phonon scattering -- the so-called supercollisions.
Determination of the path taken by a quantum particle leads to a suppression of interference and to a classical behavior. We employ here a quantum which path detector to perform accurate path determination in a two-path-electron-interferometer; leading to full suppression of the interference. Following the dephasing process we recover the interference by measuring the cross-correlation between the interferometer and detector currents. Under our measurement conditions every interfering electron is dephased by approximately a single electron in the detector - leading to mutual entanglement of approximately single pairs of electrons.
In the presence of strong interactions, electrons in condensed matter systems can behave hydrodynamically thereby exhibiting classical fluid phenomena such as vortices and Poiseuille flow. While in most conductors large screening effects minimize electron-electron interactions, hindering the search for possible hydrodynamic candidate materials, a new class of semimetals has recently been reported to exhibit strong interactions. In this work, we study the current flow in the layered semimetal tungsten ditelluride (WTe2) by imaging the local magnetic field above it using a nitrogen-vacancy (NV) defect in diamond. Our cryogenic scanning magnetometry system allows for temperature-resolved measurement with high sensitivity enabled by the long defect spin coherence. We directly measure the spatial current profile within WTe2 and find it differs substantially from the uniform profile of a Fermi liquid, indicating hydrodynamic flow. Furthermore, our temperature-resolved current profile measurements reveal an unexpected non-monotonic temperature dependence, with hydrodynamic effects strongest at ~20 K. We further elucidate this behavior via ab initio calculations of electron scattering mechanisms, which are used to extract a current profile using the electronic Boltzmann transport equation. These calculations show quantitative agreement with our measurements, capturing the non-monotonic temperature dependence. The combination of experimental and theoretical observations allows us to quantitatively infer the strength of electron-electron interactions in WTe2. We show these strong electron interactions cannot be explained by Coulomb repulsion alone and are predominantly phonon-mediated. This provides a promising avenue in the search for hydrodynamic flow and strong interactions in high carrier density materials.
In the context of describing electrons in solids as a fluid in the hydrodynamic regime, we consider a flow of electrons in a channel of finite width, i.e.~a Poiseuille flow. The electrons are accelerated by a constant electric field. We develop the appropriate relativistic hydrodynamic formalism in 2+1 dimensions and show that the fluid has a finite dc conductivity due to boundary-induced momentum relaxation, even in the absence of impurities. We use methods involving the AdS/CFT correspondence to examine the system in the strong-coupling regime. We calculate and study velocity profiles across the channel, from which we obtain the differential resistance $dV/dI$. We find that $dV/dI$ decreases with increasing current $I$ as expected for a Poiseuille flow, also at strong coupling and in the relativistic velocity regime. Moreover, we vary the coupling strength by varying $eta/s$, the ratio of shear viscosity over entropy density. We find that $dV/dI$ decreases when the coupling is increased. We also find that strongly coupled fluids are more likely to become ultra-relativistic and turbulent. These conclusions are insensitive to the presence of impurities. In particular, we predict that in channels which are clearly in the hydrodynamic regime already at small currents, the DC channel resistance strongly depends on $eta/s$.
The Coulomb interaction generally limits the quantum propagation of electrons. However, it can also provide a mechanism to transfer their quantum state over larger distances. Here, we demonstrate such a form of teleportation, across a metallic island within which the electrons are trapped much longer than their quantum lifetime. This effect originates from the low temperature freezing of the islands charge $Q$ which, in the presence of a single connected electronic channel, enforces a one-to-one correspondence between incoming and outgoing electrons. Such high-fidelity quantum state imprinting is established between well-separated injection and emission locations, through two-path interferences in the integer quantum Hall regime. The added electron quantum phase of $2pi Q/e$ can allow for strong and decoherence-free entanglement of propagating electrons, and notably of flying qubits.
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