Spin-exchange rate coefficients in Rb-Xe and Cs-Xe systems using repolarization
POSTER
Abstract
We measure and compare the spin-exchange rate coefficients Κse for Rb and Cs in a He (94%)-N2 (3%)-Xe (3%) gas mixture, similar to that used in flow-through Xe polarizers. The measurements are crucial to understanding which alkali-metal is the best partner for polarizing 129Xe; they are carried out in two matched sets (one each for Rb and Cs) of four sealed vapor cells. Combining these results with our recent spin-destruction rate results from the same samples points to which alkali-metal is intrinsically most efficient for producing large quantities of hyperpolarized Xe for applications such as medical imaging. We employed the repolarization method [1,2], where Κse = (PAεγA) / (PXe[Xe]-εPA[Xe]), and where ε is the nuclear slowing-down factor. Using optically detected pulsed EPR of the alkali-metal hyperfine structure, we measured the alkali-metal polarization PA , the alkali-metal spin-destruction rate γA due to Xe, and the 129Xe polarization PXe . The spin-destruction rate is measured “in the dark” at long delay times, in order to isolate the slowest polarization-decay component; at even longer delay times, when PA reaches a steady state due to the non-zero PXe , the so-called “back-polarization” of the alkali-metal can be determined and then calibrated by examining hyperfine peak ratios at much higher PA during active optical pumping. We calculated PXe[Xe] by using the known Rb-Xe and Cs-Xe enhancement factors (κ0)Rb and (κ0)Cs [3] and measuring the respective alkali-metal EPR frequency shifts due to polarized 129Xe. The repolarization method has the advantage of not requiring a determination of the alkali-metal number density. [1] R.K. Ghosh and M.V. Romalis, Phys. Rev. A 81, 043415 (2010); [2] B. Chann, et al., Phys. Rev. A 66, 032703 (2002); [3] S. Zou, et al., Phys. Rev. A 106, 012801 (2022).
Presenters
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Zahra Armanfard
Washington State University
Authors
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Zahra Armanfard
Washington State University
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Adnan I Nahlawi
Washington State University
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Brian T Saam
Washington State University