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We propose to use laser spectroscopy of ultracold molecules to establish improved limits on the time independence of electron-to-nuclear and nuclear-nuclear mass ratios by comparing, via an optical frequency comb, the frequencies of suitable sets of transitions in the ground electronic state. Hydrogen molecular ions trapped in a radiofrequency trap, sympathetically cooled by atomic ions, are identified as an accessible system. We show that the dipole-allowed rovibrational transition frequencies of HD^+ are suitable probes for a time dependence of m₄∕m or m∕m₃. Separate bounds on the time independence of these constants can be obtained from a comparison of HD^+ and H₂^+ transitions frequencies. Spectroscopy of single molecular ions via a quantum jump method is proposed as an approach toward ultrahigh precision.
Schiller et al. (Thu,) studied this question.