Preparation of an ultra-cold sample of ammonia molecules for precision measurements

We present experiments in which an ultra-cold sample of ammonia molecules is released from an electrostatic trap and recaptured after a variable time. It is shown that, by performing adiabatic cooling before releasing the molecules and adiabatic re-compression after they are recaptured, we are able to observe molecules even after more than 10 ms of free expansion. A coherent measurement performed during this time will have a statistical uncertainty that decreases approximately as the inverse of the square root of the expansion time. This offers interesting prospects for high-resolution spectroscopy and precision tests of fundamental physics theories.

Ramsey-type microwave spectroscopy on CO ($a^3Pi$)

Using a Ramsey-type setup, the lambda-doublet transition in the $J=1,, Omega=1$ level of the $a^3Pi$ state of CO was measured to be 394 064 870(10) Hz. In our molecular beam apparatus, a beam of metastable CO is prepared in a single quantum level by expanding CO into vacuum and exciting the molecules using a narrow-band UV laser system. After passing two microwave zones that are separated by 50 cm, the molecules are state-selectively deflected and detected 1 meter downstream on a position sensitive detector. In order to keep the molecules in a single $m_J^B$ level, a magnetic bias field is applied. We find the field-free transition frequency by taking the average of the $m_J^B = +1 rightarrow m_J^B = +1$ and $m_J^B = -1 rightarrow m_J^B = -1$ transitions, which have an almost equal but opposite Zeeman shift. The accuracy of this proof-of-principle experiment is a factor of 100 more accurate than the previous best value obtained for this transition.