Hamiltonian transformability, fast adiabatic dynamics and hidden adiabaticity

We prove the existence of a unitary transformation that enables two arbitrarily given Hamiltonians in the same Hilbert space to be transformed into one another. The result is straightforward yet, for example, it lays the foundation to implementing or mimicking dynamics with the most controllable Hamiltonian. As a promising application, this existence theorem allows for a rapidly evolving realization of adiabatic quantum computation by transforming a Hamiltonian where dynamics is in the adiabatic regime into a rapidly evolving one. We illustrate the theorem with examples.

Environmentally Induced Entanglement – Anomalous Behavior in the Adiabatic Regime

Considering two non-interacting qubits in the context of open quantum systems, it is well known that their common environment may act as an entangling agent. In a perturbative regime the influence of the environment on the system dynamics can effectively be described by a unitary and a dissipative contribution. For the two-spin Boson model with (sub-) Ohmic spectral density considered here, the particular unitary contribution (Lamb shift) easily explains the buildup of entanglement between the two qubits. Furthermore it has been argued that in the adiabatic limit, adding the so-called counterterm to the microscopic model compensates the unitary influence of the environment and, thus, inhibits the generation of entanglement. Investigating this assertion is one of the main objectives of the work presented here. Using the hierarchy of pure states (HOPS) method to numerically calculate the exact reduced dynamics, we find and explain that the degree of inhibition crucially depends on the parameter s determining the low frequency power law behavior of the spectral density J(ω)∼ωse−ω/ωc. Remarkably, we find that for resonant qubits, even in the adiabatic regime (arbitrarily large ωc), the entanglement dynamics is still influenced by an environmentally induced Hamiltonian interaction. Further, we study the model in detail and present the exact entanglement dynamics for a wide range of coupling strengths, distinguish between resonant and detuned qubits, as well as Ohmic and deep sub-Ohmic environments. Notably, we find that in all cases the asymptotic entanglement does not vanish and conjecture a linear relation between the coupling strength and the asymptotic entanglement measured by means of concurrence. Further we discuss the suitability of various perturbative master equations for obtaining approximate entanglement dynamics.

Control of atom-mirror entanglement versus Gaussian geometric discord with RWA

In this study, we control the quantum correlations existing between a movable mirror and atoms in hybrid atom-optomechanical system using rotating wave approximation (RWA) in adiabatic regime. We use the Mancini criterion to measure the entanglement, the purity to quantify the degree of mixedness and the Gaussian geometric discord (GGD) to characterize the quantum correlations even beyond entanglement. We study the effect of the optomechanical cooling rate and the cooperativity atomic on the transfer of quantum correlations between the movable mirror and atoms under the thermal effect. We also investigate the robustness of the GGD with respect to entanglement by exploiting recent experimental parameters.

Efficient analysis of stochastic gene dynamics in the non-adiabatic regime using piecewise deterministic Markov processes

Single-cell experiments show that gene expression is stochastic and bursty, a feature that can emerge from slow switching between promoter states with different activities. In addition to slow chromatin and/or DNA looping dynamics, one source of long-lived promoter states is the slow binding and unbinding kinetics of transcription factors to promoters, i.e. the non-adiabatic binding regime. Here, we introduce a simple analytical framework, known as a piecewise deterministic Markov process (PDMP), that accurately describes the stochastic dynamics of gene expression in the non-adiabatic regime. We illustrate the utility of the PDMP on a non-trivial dynamical system by analysing the properties of a titration-based oscillator in the non-adiabatic limit. We first show how to transform the underlying chemical master equation into a PDMP where the slow transitions between promoter states are stochastic, but whose rates depend upon the faster deterministic dynamics of the transcription factors regulated by these promoters. We show that the PDMP accurately describes the observed periods of stochastic cycles in activator and repressor-based titration oscillators. We then generalize our PDMP analysis to more complicated versions of titration-based oscillators to explain how multiple binding sites lengthen the period and improve coherence. Last, we show how noise-induced oscillation previously observed in a titration-based oscillator arises from non-adiabatic and discrete binding events at the promoter site.