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Paired atom laser beams created via four-wave mixing

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 Added by Graham Dennis
 Publication date 2008
  fields Physics
and research's language is English




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A method to create paired atom laser beams from a metastable helium atom laser via four-wave mixing is demonstrated. Radio frequency outcoupling is used to extract atoms from a Bose Einstein condensate near the center of the condensate and initiate scattering between trapped and untrapped atoms. The unequal strengths of the interactions for different internal states allows an energy-momentum resonance which leads to the creation of pairs of atoms scattered from the zero-velocity condensate. The resulting scattered beams are well separated from the main atom laser in the 2-dimensional transverse atom laser profile. Numerical simulations of the system are in good agreement with the observed atom laser spatial profiles, and indicate that the scattered beams are generated by a four-wave mixing process, suggesting that the beams are correlated.



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135 - A. Perrin 2008
We study atom scattering from two colliding Bose-Einstein condensates using a position sensitive, time resolved, single atom detector. In analogy to quantum optics, the process can also be thought of as spontaneous, degenerate four wave mixing of de Broglie waves. We find a clear correlation between atoms with opposite momenta, demonstrating pair production in the scattering process. We also observe a Hanbury Brown and Twiss correlation for collinear momenta, which permits an independent measurement of the size of the pair production source and thus the size of the spatial mode. The back to back pairs occupy very nearly two oppositely directed spatial modes, a promising feature for future quantum optics experiments.
We propose a method to reconstruct the vibrational quantum state of molecules excited by a general excitation laser pulse. Unlike existing methods, we do not require the molecules before excitation to be in a pure state, allowing us to treat the important case of initially thermally excited molecules. Even if only a single initial level is appreciably populated, initial levels with small populations can still give major contributions to the unknown vibrational state, making it essential to take them into account. In addition to the excitation pulse, the method uses two incident, short laser pulses in a non-co-linear geometry to create four-wave mixing in the molecules. The measurements used in the reconstruction are spectra of the outgoing four-wave mixing pulse at different time delays of the excitation laser pulse. An important point is that the method does not require detailed knowledge of molecular transition moments between excited states nor of any of the incoming laser pulses, but circumvents this requirement by using one or more calibration laser pulses in a separate experiment either before or after the main data are recorded. The only requirements for the calibration laser pulses are that the constant parts of their spectrums should together cover the spectral range of the excitation laser pulse, and the constant part of each should have sufficient spectral overlap with one other calibration pulse to populate two of the same levels. Finally, we discuss the extension of the reconstruction method in this paper to more general situations, hereby presenting the new idea of quantum state reconstruction through perturbations with calibration.
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163 - Z. Vernon , J.E. Sipe 2015
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113 - N. Mielec , M. Altorio , R. Sapam 2018
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