arXiv subjects
Publications and source records attributed to Peter Foldi.
Quantum interference and spin-orbit interaction in a one-dimensional mesoscopic semiconductor ring with one input and two output leads can act as a spin beam splitter. Different polarization can be achieved in the two output channels from an originally totally unpolarized incoming spin state, very much like in a Stern-Gerlach apparatus. We determine the relevant parameters such that the device has unit efficiency.
We discuss the effects caused by a resonant cavity around a sample of a magnetic molecular crystal (such as Mn${}_{12}$-Ac), when a time dependent external magnetic field is applied parallel to the easy axis of the crystal. We show that the back action of the cavity field on the sample significantly increases the possibility of microwave emission. This radiation process can be supperradiance or a maser-like effect, depending on the strength of the dephasing. Our model provides further insight to the theoretical understanding of the bursts of electromagnetic radiation observed in recent experiments accompanying the resonant quantum tunneling of magnetization. The experimental findings up to now can all be explained as being a maser effect rather than superradiance. The results of our theory scale similarly to the experimental findings, i.e., with increasing sweep rate of the external magnetic field, the emission peaks are shifted towards higher field values.
In this thesis concrete quantum systems are investigated in the framework of the environment induced decoherence. The focus is on the dynamics of highly nonclassical quantum states, the Wigner function of which are negative over some regions of their domains. One of the chosen physical systems is a diatomic molecule, where the potential energy of the nuclei is an anharmonic function of their distance. A system of two-level atoms, which can be important from the viewpoint of quantum information technology, is also investigated. A method is described that is valid in both systems and can determine the characteristic time of the decoherence in a dynamical way. The direction of the decoherence and its relation to energy dissipation is also studied. Finally, a scheme is proposed that can prepare decoherence-free states using the experimental techniques presently available.
In a quantum ring connected with two external leads the spin properties of an incoming electron are modified by the spin-orbit interaction resulting in a transformation of the qubit state carried by the spin. The ring acts as a one qubit spintronic quantum gate whose properties can be varied by tuning the Rashba parameter of the spin-orbit interaction, by changing the relative position of the junctions, as well as by the size of the ring. We show that a large class of unitary transformations can be attained with already one ring -- or a few rings in series -- including the important cases of the Z, X, and Hadamard gates. By choosing appropriate parameters the spin transformations can be made unitary, which corresponds to lossless gates.
The time evolution of anharmonic molecular wave packets is investigated under the influence of the environment consisting of harmonic oscillators. These oscillators represent photon or phonon modes and assumed to be in thermal equilibrium. Our model explicitly incorporates the fact that in the case of a nonequidistant spectrum the rates of the environment induced transitions are different for each transition. The nonunitary time evolution is visualized by the aid of the Wigner function related to the vibrational state of the molecule. The time scale of decoherence is much shorter than that of dissipation, and gives rise to states which are mixtures of localized states along the phase space orbit of the corresponding classical particle. This behavior is to a large extent independent of the coupling strength, the temperature of the environment and also of the initial state.
We present an algebraic method for treating molecular vibrations in the Morse potential perturbed by an external laser field. By the help of a complete and normalizable basis we transform the Schrödinger equation into a system of coupled ordinary differential equations. We apply our method to calculate the dissociation probability of the NO molecule excited by chirped laser pulses. The dependence of the molecular dipole-moment on the interatomic separation is determined by a quantum-chemical method, and the corresponding transition dipole moments are given by approximate analytic expressions. These turn out to be very small between neighboring stationary states around the vibrational quantum number $m=42$, therefore we propose to use additional pulses in order to skip this trapping state, and to obtain a reasonable dissociation probability.
The cause of decoherence in a quantum system can be traced back to the interaction with the environment. As it has been pointed out first by Dicke, in a system of N two-level atoms where each of the atoms is individually dipole coupled to the environment, there are collective, subradiant states, that have no dipole coupling to photon modes, and therefore they are expected to decay slower. This property also implies that these type of states, which form an N-1 dimensional subspace of the atomic subsytem, also decohere slower. We propose a scheme which will create such states. First the two-level atoms are placed in a strongly detuned cavity and one of the atoms, called the control atom is excited. The time evolution of the coupled atom-cavity system leads to an appropriately entangled state of the atoms. By applying subsequent laser pulses at a well defined time instant, it is possible to drive the atomic state into the subradiant, i. e., decoherence free subspace. Up to a certain average number of the photons, the result is independent of the state of the cavity. The analysis of the conditions shows that this scheme is feasible with present day techniques achieved in atom cavity interaction experiments.
We investigate the time evolution of a superposition of macroscopically distinct quantum states in a system of two-level atoms interacting with a thermal environment of photon modes. We show that the atomic coherent states are robust against decoherence, therefore we call their superpositions atomic Schrödinger cat states. The initial fast regime of the time evolution is associated with the process of decoherence, and it is directed towards the statistical mixture of the constituent coherent states of the original state for most of the initial conditions. However, certain superpositions, called symmetric, exhibit exceptionally slow decoherence. By introducing a new measure, we generalize the usual decoherence scheme regarding the evolution of the state to account also for the symmetric case. To stress the fact that the environment preserves symmetric superpositions much longer than the other ones,we present Wigner function images of the decoherence of a suitably oriented four component cat state.