Rovibrational optical cooling of a molecular beam
arXiv:1709.06797 · doi:10.1103/PhysRevA.97.031401
Abstract
Cooling the rotation and the vibration of molecules by broadband light sources was possible for trapped molecular ions or ultracold molecules. Because of a low power spectral density, the cooling timescale has never fell below than a few milliseconds. Here we report on rotational and vibrational cooling of a supersonic beam of barium monofluoride molecules in less than 440 s. Vibrational cooling was optimized by enhancing the spectral power density of a semiconductor light source at the underlying molecular transitions allowing us to transfer all the populations of into the vibrational ground state (). Rotational cooling, that requires an efficient vibrational pumping, was then achieved. According to a Boltzmann fit, the rotation temperature was reduced by almost a factor of 10. In this fashion, the population of the lowest rotational levels increased by more than one order of magnitude.
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Cited by in corpus (10)
- Controlling the scattering length of ultracold dipolar molecules
- Buffer-gas cooling, high-resolution spectroscopy and optical cycling of barium monofluoride molecules
- Cooling of a Zero-Nuclear-Spin Molecular Ion to a Selected Rotational State
- Lifetime Measurements of the and States in BaF
- Saturated absorption spectroscopy of buffer-gas-cooled Barium monofluoride molecules
- Generation of rotational ground state HD ions in an ion trap using a resonance-enhanced threshold photoionization process
- Laser cooling of barium monofluoride molecules using synthesized optical spectra
- Isotopologue-selective laser cooling of molecules
- Determining a vibrational distribution with a broadband optical source
- Photon spin molasses for laser cooling molecular rotation