Quantum systems engineering

Abstract:

The light-matter interaction can be utilized to qualitatively alter physical properties of materials. Recent theoretical and experimental studies have explored this possibility of controlling matter by light based on driving many-body systems via strong classical electromagnetic radiation, leading to a time-dependent Hamiltonian for electronic or lattice degrees of freedom. To avoid inevitable heating, pump-probe setups with ultrashort laser pulses have so far been used to study transient light-induced modifications in materials. Here, we pursue yet another direction of controlling quantum matter by modifying quantum fluctuations of its electromagnetic environment. In contrast to earlier proposals on light-enhanced electron-electron interactions, we consider a dipolar quantum many-body system embedded in a cavity composed of metal mirrors and formulate a theoretical framework to manipulate its equilibrium properties on the basis of quantum light-matter interaction. We analyze hybridization of different types of the fundamental excitations, including dipolar phonons, cavity photons, and plasmons in metal mirrors, arising from the cavity confinement in the regime of strong light-matter interaction. This hybridization qualitatively alters the nature of the collective excitations and can be used to selectively control energy-level structures in a wide range of platforms. Most notably, in quantum paraelectrics, we show that the cavity-induced softening of infrared optical phonons enhances the ferroelectric phase in comparison with the bulk materials. Our findings suggest an intriguing possibility of inducing a superradiant-type transition via the light-matter coupling without external pumping. We also discuss possible applications of the cavity-induced modifications in collective excitations to molecular materials and excitonic devices.

Abstract:

Spin-charge separation (SCS) is a striking manifestation of strong correlations in low-dimensional quantum systems, whereby a fermion splits into separate spin and charge excitations that travel at different speeds. Here, we demonstrate that periodic driving enables control over SCS in a Hubbard system near half filling. In one dimension, we predict analytically an exotic regime where charge travels slower than spin and can even become “frozen,” in agreement with numerical calculations. In two dimensions, the driving slows both charge and spin and leads to complex interferences between single-particle and pair-hopping processes.

Abstract:

In triangular lattice structures, spatial anisotropy and frustration can lead to rich equilibrium phase diagrams with regions containing complex, highly entangled states of matter. In this work, we study the driven two-rung triangular Hubbard model and evolve these states out of equilibrium, observing how the interplay between the driving and the initial state unexpectedly shuts down the particle-hole excitation pathway. This restriction, which symmetry arguments fail to predict, dictates the transient dynamics of the system, causing the available particle-hole degrees of freedom to manifest uniform long-range order. We discuss implications of our results for a recent experiment on photoinduced superconductivity in κ − ( BEDT − TTF ) 2 Cu [ N ( CN ) 2 ] Br molecules.

Abstract:

We discuss the emergence of non-stationarity in open quantum many-body systems. This leads us to the definition of dissipative time crystals which display experimentally observable, persistent, time-periodic oscillations induced by noisy contact with an environment. We use the Loschmidt echo and local observables to indicate the presence of a finite sized dissipative time crystal. Starting from the closed Hubbard model we then provide examples of dissipation mechanisms that yield experimentally observable quantum periodic dynamics and allow analysis of the emergence of finite sized dissipative time crystals. For a disordered Hubbard model including two-particle loss and gain we find a dark Hamiltonian driving oscillations between GHZ states in the long-time limit. Finally, we discuss how the presented examples could be experimentally realized.

Abstract:

The properties of organic conductors are often tuned by the application of chemical or external pressure, which change orbital overlaps and electronic bandwidths while leaving the molecular building blocks virtually unperturbed. Here, we show that, unlike any other method, light can be used to manipulate the local electronic properties at the molecular sites, giving rise to new emergent properties. Targeted molecular excitations in the charge-transfer salt κ−(BEDT−TTF)2 Cu[N(CN)2] Br induce a colossal increase in carrier mobility and the opening of a superconducting optical gap. Both features track the density of quasiparticles of the equilibrium metal and can be observed up to a characteristic coherence temperature T∗≃50K, far higher than the equilibrium transition temperature TC=12.5K. Notably, the large optical gap achieved by photoexcitation is not observed in the equilibrium superconductor, pointing to a light-induced state that is different from that obtained by cooling. First-principles calculations and model Hamiltonian dynamics predict a transient state with long-range pairing correlations, providing a possible physical scenario for photomolecular superconductivity.