Affiliation:
1. Instituto de Física Fundamental (IFF–CSIC), Serrano 123, 28006 Madrid, Spain.
Abstract
Effective descriptions accounting for the evolution of quantum systems that are acted on by a bath are desirable. As the number of bath degrees of freedom increases and full quantum simulations turn out computationally prohibitive, simpler models become essential to understand and gain an insight into the main physical mechanisms involved in the system dynamics. In this regard, vibrational decoherence of an I2 diatomics is tackled here within the framework of Markovian quantum state diffusion. The I2 dynamics are analyzed in terms of an effective decoherence rate, Λ, and the specific choice of the initial state, in particular, Gaussian wave packets and two-state superpositions. It is found that, for Markovian baths, the relevant quantity regarding decoherence is the product of friction (η) and temperature (T); there is no distinction between varying one or the other. It is also observed that decoherence becomes faster as the energy levels involved in the system state correspond to higher eigenvalues. This effect is due to a population redistribution during the dynamical process and an eventual irreversible loss of the initial coherence. These results have been compared with those available in the literature from more detailed semiclassical IVR simulations, finding a good agreement.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
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