Abstract
This paper presents a detailed analysis of the effect of the optical lattice field on clock transition spectroscopy, as exemplified by thulium atoms. We consider the applicability of the sifting of atoms in an optical lattice by ramping down the power of the laser light that produces it. This method allows the number of filled vibrational sublevels to be reduced down to a single vibrational state, without changing the inner state of the atoms. The effectiveness of the method is illustrated by the example of the spectroscopy of a clock transition in thulium atoms in the resolved sideband regime.
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