Internal state thermometry of cold trapped molecular anions
arXiv:1408.4968 · doi:10.1039/C2CP43186F
Abstract
Photodetachment spectroscopy of OH- and H3O2- anions has been performed in a cryogenic 22-pole radiofrequency multipole trap. Measurements of the detachment cross section as a function of laser frequency near threshold have been analysed. Using this bound-free spectroscopy approach we could demonstrate rotational and vibrational cooling of the trapped anions by the buffer gas in the multipole trap. Below 50 K the OH- rotational temperature shows deviations from the buffer gas temperature, and possible causes for this are discussed. For H3O2- vibrational cooling of the lowest vibrational quantum states into the vibrational ground state is observed. Its photodetachment cross section near threshold is modelled with a Franck-Condon model, with a detachment threshold that is lower, but still in agreement with the expected threshold for this system.
References in corpus (1)
Cited by in corpus (5)
- Radiative rotational lifetimes and state-resolved relative detachment cross sections from photodetachment thermometry of molecular anions in a cryogenic storage ring
- Incomplete rotational cooling in a 22-pole ion trap
- Direct Observation of High-Spin States in Manganese Dimer and Trimer Cations by X-ray Magnetic Circular Dichroism Spectroscopy in an Ion Trap
- Spectroscopy and ion thermometry of C using laser-cooling transitions
- Determining a vibrational distribution with a broadband optical source