Abstract

Photoexcitation rates for creation of ultralong-range Rydberg molecules with 31 ≲ n ≲ 41 in both ground and excited vibrational levels in cold (T ∼ 900 nK) gases of polarized and unpolarized 87Sr are presented. The measured production rates of the ν = 0, 1 and 2 vibrational levels reveal rather different n dependences which are analyzed by evaluating the Franck–Condon factors associated with excitation of the different vibrational levels and molecular rotational states. In particular, for gases of spin-polarized fermions, only Rydberg dimers with odd rotational quantum numbers are excited due to the requirement that their wave functions be anti-symmetric with respect to exchange. The data also demonstrate that measurements of the formation of vibrationally-excited ν = 1 molecules can furnish a probe of pair correlations over intermediate length scales.

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