The authors review the theory of the harmonic oscillator with time-dependent frequency by means of an approach based on an operator constant of the motion. With the help of this operator constant we define the ground state, the excited states and a coherent state of the oscillator and discuss the time dependence of these states through their Wigner functions. The authors derive the Wigner function of an arbitrary state at time t evolving in the time-dependent harmonic potential. Moreover, they calculate the correlation coefficient between position and momentum, which appears in the Schrodinger uncertainty relation. The authors illustrate their results for the example of a charged particle in the Paul trap.
The statistical properties of systems of coupled quantum-mechanical harmonic oscillators are analyzed. The Hamiltonian for the system is assumed to be an inhomogeneous quadratic form in the creation and annihilation operators, and is allowed to have an explicit time dependence. The relationship to classical theory is emphasized by expressing pure states in terms of the coherent-state vectors, and density operators by means of the
P representation and an analogous representation involving the Wigner function. The state which evolves from an initially coherent state of the system is found, and equations governing the time evolution of the Wigner function and the weight function for the
P representation are derived, in differential and integral form, for arbitrary initial states of the system. The results remain valid for couplings which do not preserve the vacuum state, and for cases in which the time dependence of the coupling parameters gives rise to large-scale amplification of the initial field intensities. The analysis is performed by first treating general linear inhomogeneous canonical transformations on the oscillator variables, and then specializing to the case in which these transformations represent the solutions for the Heisenberg operators in terms of their initial values. The results are illustrated within the context of a model of parametric amplification.
We investigate the quantum entanglement dynamics of two coupled harmonic oscillators with a time-dependent interaction. Using the Lewis-Riesenfeld invariant method, we derive the exact analytical wave functions without any perturbative or adiabatic approximations and combine this with a phase-space analysis using the Wigner function to provide a complete description of the system's quantum state evolution. We obtain general expression form for the purity and the linear entropy
SL=1−P for arbitrary excitation numbers
(n,m), allows a systematic study of entanglement for a large class of quantum states. We show that the entanglement dynamics is very sensitive to the interplay between the detuning parameters
θ and
ϑ2, the frequency parameter
β0 and the coupling strength
ε: the increase of detuning takes the system from slow irregular oscillations to fast and regular periodic behavior, and the stronger coupling systematically enhances both the amplitude and the average value of the linear entropy. Most importantly, for the resonance case
ω1=ω2=1 and strong couplings
ε≈0.99, the system shows robust undamped synchronized periodic oscillations of the linear entropy for all quantum states considered, indicating preserved quantum coherence without saturation. Our findings demonstrate that linear entropy is a sensitive and practical entanglement witness, and we establish explicit analytical relations between the coupling parameters of the system and its entanglement properties, which are directly relevant to quantum information processing and the control of quantum correlations in continuous-variable systems.
Solutions of the Schrödinger equation with an exact time dependence are derived as eigenfunctions of dynamical invariants which are constructed from time-independent operators using time-dependent unitary transformations. Exact solutions and a closed form expression for the corresponding time evolution operator are found for a wide range of time-dependent Hamiltonians in d dimensions, including non-Hermitean -symmetric Hamiltonians. Hamiltonians are constructed using time-dependent unitary spatial transformations comprising dilatations, translations and rotations and solutions are found in several forms: as eigenfunctions of a quadratic invariant, as coherent state eigenfunctions of boson operators, as plane wave solutions from which the general solution is obtained as an integral transform by means of the Fourier transform, and as distributional solutions for which the initial wavefunction is the Dirac δ-function. For the isotropic harmonic oscillator in d dimensions radial solutions are found which extend known results for d = 1, including Barut–Girardello and Perelomov coherent states (i.e., vector coherent states), which are shown to be related to eigenfunctions of the quadratic invariant by the ζ-transformation. This transformation, which leaves the Ermakov equation invariant, implements SU(1, 1) transformations on linear dynamical invariants. coherent states are derived also for the time-dependent linear potential. Exact solutions are found for Hamiltonians with electromagnetic interactions in which the time-dependent magnetic and electric fields are not necessarily spatially uniform. As an example, it is shown how to find exact solutions of the time-dependent Schrödinger equation for the Dirac magnetic monopole in the presence of time-dependent magnetic and electric fields of a specified form.
In the present communication we introduce the transformed Tavis–Cummings problem as a physical model to discuss constants of the motion (invariants) for such a system. The Hamiltonian we have used can be regarded as a most general time-dependent frequency converter model. The advantage of the present work is to handle a real physical problem which represents the interaction between two coupled oscillators. In this context we obtained real and complex classes of linear and quadratic invariants. We have employed the real quadratic invariants to define a new Dirac operator, from which the wavefunction in the coherent states is obtained.