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Journal of Superconductivity and Novel Magnetism

Dynamic of Quantum Correlations in Oscillating Molecules

Sodeif Ahadpour, Фороузан Мирмасоуди

Published Aug 6, 2020• 1 citation
Publisher
DOI
10.1007/s10948-020-05604-0

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An unstable condensate of diatomic molecules will coherently disassociate into correlated pairs of atoms. This dissociation process exhibits very rich quantum dynamics depending on the quantum statistics of the constituent atoms. We show that in the case of bosonic atoms Bose enhancement can lead to stimulated dissociation, whereas, in the case of fermions Pauli blocking of the available states and a buildup of coherence between molecules and atom pairs can give rise to incomplete dissociation of the molecules and transient association-dissociation oscillations.
Abstract We consider two ultracold polar symmetric top molecules coupled by dipole-dipole interaction in an external electric field with appreciable intensity gradient, serving as the physical carrier of quantum information. Each molecule is induced to undergo pendular oscillations under the strong static electric field. Based on the pendular states of polar symmetric top molecules as candidate qubits, we investigate the bipartite quantum correlations of the two polar molecular system for the thermal equilibrium states, characterized by negativity and quantum discord, and then analyze the corresponding coherence, measured by relative entropy and l1 norm. Furthermore, we also examine the dynamics of the entanglement and coherence of the system in the presence of intrinsic decoherence, and explore the relations of their temporal evolution with various physical system parameters for two different initial Bell states. It is found that quantum correlations and coherence of the two polar molecules in pendular states can be manipulated by adjusting appropriate reduced variables including external electric field, dipole-dipole interaction, ambient temperature and decoherence factor. Our findings could be used for molecular quantum computing based on rotational states.
Fluorescence photons emitted by a single molecule trapped in a solid at low temperature are correlated in time. A simple theory of the correlation pattern is presented, including in the same formalism photon antibunching from coherent Rabi oscillations and photon bunching due to incoherent quantum transitions between electronic levels. The correlation method is applied to single pentacene molecules in a para-terphenyl crystal. A clear photon bunching allows us to determine the ISC rates for each molecule. We attribute the scatter of our results for the transition rate between excited singlet and triplet states, and the difference with the average value taken from the literature, to molecular distortions induced by crystal defects in our small sample. We conclude that the correlation method associated to single molecule spectroscopy has a great potential to study dynamical processes on intermediate time scales in condensed matter.