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Bulletin of the American Physical Society

Planned Efficiency Measurements of STIRAP

В.А. Захаров, Casey McKenna, Deqian Yuan, Jessica Gasparik, Harold J. Metcalf

Published Jun 10, 2015• 0 citations
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Improving the stimulated Raman adiabatic passage efficiency for ultracold 6Li40K ground state molecules

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Abstract Ultracold polar molecules represent a rapidly advancing platform at the forefront of quantum simulation, quantum computation, quantum chemistry, and precision measurement. We report an experimental investigation for improving the creation efficiency of ultracold 6Li40K ground state molecules using stimulated Raman adiabatic passage (STIRAP). We address laser amplitude/phase noise and polarization impurity to improve STIRAP efficiency. The phase noise of our two Raman lasers is suppressed effectively by extending the cavity length for the external-cavity diode lasers (ECDLs). Further, we find that even a weak polarization impurity significantly reduces the STIRAP efficiency on the single-photon resonance (Δ = 0) for 6Li40K, due to coupling to undesired molecular levels. However, STIRAP efficiencies over 90% can be achieved by increasing Δ/2π to 10 MHz, which is comparable to the excited-state scattering rate. Our work holds significance for achieving efficient STIRAP transfer in ultracold molecules with unresolved excited-state hyperfine splittings and large scattering rates.

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Robust Population Transfer by Stimulated Raman Adiabatic Passage in a Pr3+:Y2SiO5 Crystal

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We report on the experimental implementation of stimulated Raman adiabatic passage (STIRAP) in a Pr3+:Y2SiO5 crystal. Our data provide clear and striking proof for nearly complete population inversion between hyperfine levels in the Pr3+ ions. The transfer efficiency was monitored by absorption spectroscopy. Time-resolved absorption measurements serve to monitor the adiabatic population dynamics during the STIRAP process. Efficient transfer is observed for negative pulse delays (STIRAP), as well as for positive delays. We identify the latter by an alternative adiabatic passage process.

Physical Review Letters•Sep 14, 2007•112 citations
Abstract Ultracold polar molecules represent a rapidly advancing platform at the forefront of quantum simulation, quantum computation, quantum chemistry, and precision measurement. We report an experimental investigation for improving the creation efficiency of ultracold 6Li40K ground state molecules using stimulated Raman adiabatic passage (STIRAP). We address laser amplitude/phase noise and polarization impurity to improve STIRAP efficiency. The phase noise of our two Raman lasers is suppressed effectively by extending the cavity length for the external-cavity diode lasers (ECDLs). Further, we find that even a weak polarization impurity significantly reduces the STIRAP efficiency on the single-photon resonance (Δ = 0) for 6Li40K, due to coupling to undesired molecular levels. However, STIRAP efficiencies over 90% can be achieved by increasing Δ/2π to 10 MHz, which is comparable to the excited-state scattering rate. Our work holds significance for achieving efficient STIRAP transfer in ultracold molecules with unresolved excited-state hyperfine splittings and large scattering rates.
We have set up a STIRAP excitation mechanism for helium from the metastable 23S state into Rydberg states, via the intermediate level 33P . A uv laser at 389 nm and an ir laser at 780-815nm are used as the pump and Stokes beams respectively. Our purposes is to examine how well STIRAP works to efficiently produce the Rydberg atoms, and also to apply STIRAP for further coherent manipulations of helium. To examine the efficiency of the STIRAP process, we use the state selectivity of the light force on atoms to physically separate atoms with different internal states. We use the bichromatic force on a transition different from those used for Rydberg excitation. We do not measure an excitation efficiency close to the ~100% theoretical optimum but instead only about 50%. To gain more insight into this coherent process, an excitation path interferometer is envisioned that showes the expected interference, via the final population of the Rydberg level.
We report on the experimental implementation of stimulated Raman adiabatic passage (STIRAP) in a Pr3+:Y2SiO5 crystal. Our data provide clear and striking proof for nearly complete population inversion between hyperfine levels in the Pr3+ ions. The transfer efficiency was monitored by absorption spectroscopy. Time-resolved absorption measurements serve to monitor the adiabatic population dynamics during the STIRAP process. Efficient transfer is observed for negative pulse delays (STIRAP), as well as for positive delays. We identify the latter by an alternative adiabatic passage process.