Unresolved sideband photon recoil spectroscopy of molecular ions
arXiv:2004.02959 · doi:10.1103/PhysRevA.105.063709
Abstract
We reflect on the prospect of exploiting the recoil associated with absorption and emission of photons to perform spectroscopy of a single molecular ion. For this recoil to be detectable, the molecular ion is sympathetically cooled by a laser-cooled atomic ion to near their common quantum mechanical ground state within a trapping potential. More specifically, we present a general framework for simulating the expected photon recoil spectra in regimes where either the natural transition linewidth of the molecular ion or the spectral width of the exciting light source exceeds the motional frequencies of the two-ion system. To exemplify the framework, we present two complementary cases: spectroscopy of the broad 3s S - 3p P electronic transition ( MHz) of a single Mg ion at nm by a narrow laser source ( MHz) and mid-infrared vibrational spectroscopy of the very narrow - transition ( Hz) at m in the electronic ground state of MgH by a broadband laser source ( 50 MHz). The atomic ion Mg has been picked to introduce a simple system to make comparisons with experimental results while still capturing most of the physics involved in electronic excitations of molecular ions.
20 pages, 19 figures
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