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APS

Spectroscopic analysis of the ( 2 )^3σ^+ state of ^41K ^87Rb towards ultracold rovibronic ground-state molecules

K. Aikawa, Jun Kobayashi, Masahito Ueda, S. Inouye

Published Mar 1, 2010• 0 citations
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Abstract We spectroscopically investigate a pathway for the conversion of 23Na39K Feshbach molecules into rovibronic ground state molecules via stimulated Raman adiabatic passage. Using photoassociation spectroscopy from the diatomic scattering threshold in the a 3Σ+ potential, we locate the resonantly mixed electronically excited intermediate states ∣ B 1 Π , v = 8 〉 and ∣ c 3 Σ + , v = 30 〉 which, due to their singlet–triplet admixture, serve as an ideal bridge between predominantly a 3Σ+ Feshbach molecules and pure X 1Σ+ ground state molecules. We investigate their hyperfine structure and present a simple model to determine the singlet–triplet coupling of these states. Using Autler–Townes spectroscopy, we locate the rovibronic ground state of the 23Na39K molecule ( ∣ X 1 Σ + , v = 0 , N = 0 〉 ) and the second rotationally excited state N = 2 to unambiguously identify the ground state. We also extract the effective transition dipole moment from the excited to the ground state. Our investigations result in a fully characterized scheme for the creation of ultracold bosonic 23Na39K ground state molecules.

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Theory and spectroscopy for ultracold KRb molecules

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Progress towards Direct Photoassociative Formation of Ultracold KRb Molecules in the lowest rovibronic state $X\,^1\Sigma^+, v=0, N=0$

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Bulletin of the American Physical Society•Jun 15, 2011•0 citations
Spectroscopic analysis of the (2)3Σ+\left( 2 \right)^3\Sigma ^+(2)3Σ+ state of ${ }^{\mbox{41}}\mbox{K}{ }^{\mbox{87}}\mbox{Rb}$ towards ultracold rovibronic ground-state molecules
Abstract We spectroscopically investigate a pathway for the conversion of 23Na39K Feshbach molecules into rovibronic ground state molecules via stimulated Raman adiabatic passage. Using photoassociation spectroscopy from the diatomic scattering threshold in the a 3Σ+ potential, we locate the resonantly mixed electronically excited intermediate states ∣ B 1 Π , v = 8 〉 and ∣ c 3 Σ + , v = 30 〉 which, due to their singlet–triplet admixture, serve as an ideal bridge between predominantly a 3Σ+ Feshbach molecules and pure X 1Σ+ ground state molecules. We investigate their hyperfine structure and present a simple model to determine the singlet–triplet coupling of these states. Using Autler–Townes spectroscopy, we locate the rovibronic ground state of the 23Na39K molecule ( ∣ X 1 Σ + , v = 0 , N = 0 〉 ) and the second rotationally excited state N = 2 to unambiguously identify the ground state. We also extract the effective transition dipole moment from the excited to the ground state. Our investigations result in a fully characterized scheme for the creation of ultracold bosonic 23Na39K ground state molecules.
Progress towards Direct Photoassociative Formation of Ultracold KRb Molecules in the lowest rovibronic state X 1Σ+,v=0,N=0X\,^1\Sigma^+, v=0, N=0X1Σ+,v=0,N=0