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Bulletin of the American Physical Society

Toward Triplet Ground State LiNa Molecules

Sepehr Ebadi, Alan O. Jamison, Timur M. Rvachov, Li Jing, Hyungmok Son, Yijun Jiang, Martin W. Zwierlein, Wolfgang Ketterle

Published Jun 11, 2015• 0 citations
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All Optical Scheme for Strongly Enhanced Production of Dipolar Molecules in the Electro-Vibrational Ground State

Matt Mackie, Catherine DeBrosse

We consider two-color heteronuclear photoassociation of atoms into dipolar molecules in the J=1 electro-vibrational ground state, where a free-ground laser couples atoms directly to the ground state and a free-bound laser couples the atoms to an electronically-excited state. This problem raises an interest because heteronuclear photoassociation from atoms to near-ground state molecules is limited by the small size of the target state. Nevertheless, the addition of the excited state creates a second pathway for creating ground state molecules, leading to quantum interference between direct photoassociation and photoassociation via the excited molecular state, as well as a dispersive-like shift of the free-ground resonance position. Using LiNa as an example, these results are shown to depend on the detuning and intensity of the free-bound laser, as well as the semi-classical size of both molecular states. Despite strong enhancement, coherent conversion to the LiNa electro-vibrational ground state is possible only in a limited regime near the free-bound resonance.

arXiv:0911.3167•Nov 16, 2009•0 citations
We consider two-color heteronuclear photoassociation of atoms into dipolar molecules in the J=1 electro-vibrational ground state, where a free-ground laser couples atoms directly to the ground state and a free-bound laser couples the atoms to an electronically-excited state. This problem raises an interest because heteronuclear photoassociation from atoms to near-ground state molecules is limited by the small size of the target state. Nevertheless, the addition of the excited state creates a second pathway for creating ground state molecules, leading to quantum interference between direct photoassociation and photoassociation via the excited molecular state, as well as a dispersive-like shift of the free-ground resonance position. Using LiNa as an example, these results are shown to depend on the detuning and intensity of the free-bound laser, as well as the semi-classical size of both molecular states. Despite strong enhancement, coherent conversion to the LiNa electro-vibrational ground state is possible only in a limited regime near the free-bound resonance.