In optical dipole traps, the excited rotational states of a molecule may experience a very different light shift than the ground state. For particles with two polarizability components (parallel and perpendicular), such as linear Σ molecules, the differential shift can be nulled by choice of elliptical polarization. When one component of the polarization vector is ±i2 times the orthogonal component, the light shift for a sublevel of excited rotational states ±approaches that of the ground state at high optical intensity. In this case, fluctuating trap intensity need not limit coherence between ground and excited rotational states.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1364/OE.26.019821 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!