Quantum state preparation and control of single molecular ions
arXiv:1109.0208 · doi:10.1088/1367-2630/14/2/023029
Abstract
Preparing molecules at rest and in a highly pure quantum state is a long standing dream in chemistry and physics, so far achieved only for a select set of molecules in dedicated experimental setups. Here, a quantum-limited combination of mass spectrometry and Raman spectroscopy is proposed that should be applicable to a wide range of molecular ions. Excitation of electrons in the molecule followed by uncontrolled decay and branching into several lower energy states is avoided. Instead, the molecule is always connected to rotational states within the electronic and vibrational ground-state manifold, while a co-trapped atomic ion provides efficient entropy removal and allows for extraction of information on the molecule. The outlined techniques might enable preparation, manipulation and measurement of a large multitude of molecular ion species with the same instrument, with applications including, but not limited to, precise determination of molecular properties and fundamental tests of physics.
12 pages, 2 figures, reformatted for resubmission
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- Two-photon vibrational transitions in as probes of variation of the proton-to-electron mass ratio
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- Quantum Computation with Rotational States of Nonpolar Ionic Molecules
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- Ultrafast infrared spectroscopy with single molecular ions
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