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Physical Review A

Control of dephasing in rotationally hot molecules

David Bartram, Misha Ivanov

Published Apr 12, 2010• 3 citations
Publisher

Abstract

We consider a rotationally hot diatomic molecule as an example of an open quantum system, where molecular vibrational wave packets are subject to dephasing due to rovibrational coupling. We report analytical and numerical results addressing whether the dephasing rate can be controlled by adjustment of the initial wave packet phases. It appears that over long time scales, phase-only control is not possible, but for earlier time scales the possibility of phase-only control of dephasing remains. In addition, we point out that the time dependence of the dephasing process depends significantly upon the degeneracy of the rotational environment states.

DOI
10.1103/physreva.81.043405

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We consider a rotationally hot diatomic molecule as an example of an open quantum system, where molecular vibrational wave packets are subject to dephasing due to rovibrational coupling. We report analytical and numerical results addressing whether the dephasing rate can be controlled by adjustment of the initial wave packet phases. It appears that over long time scales, phase-only control is not possible, but for earlier time scales the possibility of phase-only control of dephasing remains. In addition, we point out that the time dependence of the dephasing process depends significantly upon the degeneracy of the rotational environment states.
In this thesis, we discuss the possibilities for suppression of decoherence, the loss of purity in an open quantum system, and the related process of dephasing. In the first chapter, we review the literature on the subject of open system dynamics, decoherence and methods of decoherence suppression. In the second chapter, we focus on the specific case of a rotationally hot diatomic molecule as an example of an open quantum system, where molecular vibrational wavepackets are subject to dephasing due to rovibrational coupling. We report analytical and numerical results addressing whether the dephasing rate can be controlled by adjustment of the initial wavepacket phases. It appears that over long timescales, phase-only control is not possible, but for earlier timescales the possibility of phase-only control of dephasing remains. In addition, we point out that the time-dependence of the dephasing process depends significantly upon the degeneracy of the rotational environment states. In the final chapter, we discuss the same system, but apply a qualitatively different method of dephasing suppression based on the nonlinear resonance effect in a driving field. We extend previous work on the topic (Shapiro et al. [1]) by considering the effect of using a train of laser pulses as the driving field, in place of a two-colour continuous-wave laser field. We demonstrate that the pulse train method can be more effective at suppressing dephasing than the two-colour CW case.
Any real system, no matter how well isolated, unavoidably interacts with the environment. This interaction makes the evolution of a quantum system nonunitary and destroys the coherence of quantum superpositions. This process, known as decoherence, is widely regarded as the most important and fundamental obstacle to the practical realization of quantum information processing. On the other hand, the objectives of quantum control are predicated on the ability to manipulate the system coherently over a period of time. Quantum control has been applied successfully to several experimental systems and coupling such a controlled system to an environment makes the study of coherence loss possible. The standard model of decoherence is formulated in terms of a system, defined by the observables that can be measured, and a reservoir, de¯ned by those degrees of freedom that are not accessed by observation. The vibrational and rotational degree of freedom of diatomic molecules form an experimental model of such a system and bath 1. The nature of the ro-vibrational coupling does not allow a Decoherence Free Subspace, instead we try to identify a Decoherence Resistant Subspace using closed loop control. We set up a learning control loop experiment to monitor the coherence in a vibrational wavepacket, consisting of about 6 vibrational states of the A(1Σ+g ) electronic state, excited by a shaped, ultrashort optical pulse, and then to determine the pulse shape that yielded the longest coherence lifetime. The coherence of the vibrational wavepacket was monitored by measuring the fluorescence quantum beats from the outer turning point of the wave packet's trajectory. The closed loop controller altered the shape of the driving optical pulse to maximize the the depth of modulation of the quantum beats at a prescribed time after excitation, within the constraints of the laser system. The outcome of this closed loop control experiment shows an improvement of the beat decay constant of about 60%, as shown in Fig. (1), a result which occurs for several di®erent pulse shapes. Our experiments show that a number of interesting decoherence-resistant excitations exist. The nature of the dephasing was examined theoretically. Using measured optical pulse shapes, we simulated numerically the molecular wavepacket in the limit of perturbation theory. The experiment and simulations show that there are di®erent mechanisms contributing to the decoherence resistant excitation. The shaped pulse reduces the °uctuations in the wave packet spatial extent, which in turn changes the system reservoir coupling. Other components of the optimal pulse are a sequence of pulses that creates constructive interference of the vibrational wavepacket at the desired time, and chirp which compensates for the anharmonicity of the adiabatic potential. The experimental results show general agreement with numerical simulations. We conclude that wavepackets resistant to dephasing do exist,and that learning algorithms provide an effcient means for finding them.
We report an experimental and theoretical study of the evolution of vibrational coherence in a thermal ensemble of nitrogen molecules. Rotational dephasing and rephasing of the vibrational coherence is detected by coherent anti-Stokes Raman scattering. The existence of rovibrational coupling and the discrete energy spectrum of the rotational bath lead to a whole new class of full and fractional rovibrational revivals. Following the rich rovibrational dynamics on a nanosecond time scale with subpicosecond time resolution enables us to determine the second-order rovibrational constant ${\ensuremath{\gamma}}_{e}$ and assess new possibilities of controlling decoherence.
An intuitive scheme for controlling the rotational quantum state of a Rydberg molecule is demonstrated experimentally. We determine the accumulated phase difference between the various components of a molecular electron wave packet, and then employ a sequence of phase-locked optical pulses to selectively enhance or depopulate specific rotational states. The angular momentum composition of the resulting wave packet, and the efficiency of the control scheme, is determined by calculating the multipulse response of the time-dependent Rydberg populations.
We investigate the dynamics of a rotating Morse wave packet, appropriate for a ro-vibrating diatomic molecule. The coupling between vibrational and rotational degrees of freedom is explicated in real position space as well as in phase space Wigner distribution of a SU(2) coherent state at various dynamically evolved times. We choose the well studied I2I_{2}I2​ molecule with the parameter values in good agrement with experiments. A quantitative measure of the angles of rotations for different angular momenta is also given.