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The ability to prepare molecular ions in selected quantum states enables studies in areas such as chemistry, metrology, spectroscopy, quantum information, and precision measurements. Here, we demonstrate (2 + 1) resonance-enhanced multiphoton ionization (REMPI) of oxygen, both in a molecular beam and in an ion trap. The two-photon transition in the REMPI spectrum is rotationally resolved, allowing ionization from a selected rovibrational state of O2. Fits to this spectrum determine spectroscopic parameters of the O2d1Πg state and resolve a discrepancy in the literature regarding its band origin. The trapped molecular ions are cooled by co-trapped atomic ions. Fluorescence mass spectrometry nondestructively demonstrates the presence of the photoionized O2+. We discuss strategies for maximizing the fraction of ions produced in the ground rovibrational state. For (2 + 1) REMPI through the d1Πg state, we show that the Q(1) transition is preferred for neutral O2 at rotational temperatures below 50 K, while the O(3) transition is more suitable at higher temperatures. The combination of state-selective loading and nondestructive detection of trapped molecular ions has applications in optical clocks, tests of fundamental physics, and control of chemical reactions.
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Dipole–phonon quantum logic with alkaline-earth monoxide and monosulfide cations
Dipole–phonon quantum logic (DPQL) leverages the interaction between polar molecular ions and the motional modes of a trapped-ion Coulomb crystal to provide a potentially scalable route to quantum information science. Here, we study a class of candidate molecular ions for DPQL, the cationic alkaline-earth monoxides and monosulfides, which possess suitable structure for DPQL and can be produced in existing atomic ion experiments with little additional complexity. We present calculations of DPQL operations for one of these molecules, CaO + , and discuss progress towards experimental realization. We also further develop the theory of DPQL to include state preparation and measurement and entanglement of multiple molecular ions.
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- PAR ID:
- 10251414
- Date Published:
- Journal Name:
- Physical Chemistry Chemical Physics
- Volume:
- 22
- Issue:
- 43
- ISSN:
- 1463-9076
- Page Range / eLocation ID:
- 24964 to 24973
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/D0CP04574H
