Entanglement between electronic and vibrational degrees of freedom in a laser-driven molecular system
arXiv:1402.6959 · doi:10.1103/PhysRevA.88.063415
Abstract
We investigate the entanglement between electronic and vibrational degrees of freedom produced by a vibronic coupling in a molecular system described in the Born-Oppenheimer approximation. Entanglement in a pure state of the Hilbert space is quantified using the von Neumann entropy of the reduced density matrix and the reduced linear entropy. Expressions for these entanglement measures are derived for the and cases of the bipartite entanglement, where 2 and 3 are the dimensions of the electronic Hilbert space , and is the dimension of . We study the entanglement dynamics for two electronic states coupled by a laser pulse (a case), taking as an example a coupling between the and states of the Cs molecule. The reduced linear entropy expression obtained for the case is used to follow the entanglement evolution in a scheme proposed for the control of the vibronic dynamics in a Cs cold molecule, implying the , , and electronic states, which are coupled by a non-adiabatic radial coupling and a sequence of chirped laser pulses.
30 pages, 8 figures
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