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Bulletin of the American Physical Society

Hyperfine quenching rates of $nsnp\,^3P_0-ns^2\,^1S_0$ transition in $^{25}$Mg, $^{87}$Sr and $^{113}$Cd

Z. Zuhrianda, Safronova

Published Oct 16, 2016• 0 citations
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S. G. Porsev, Andrei Derevianko

Hyperfine quenching rates of the lowest-energy metastable $^{3}P_{0}$ and $^{3}P_{2}$ states of Mg, Ca, Sr, and Yb atoms are computed. The calculations are carried out using ab initio relativistic many-body methods. The computed lifetimes may be useful for designing novel ultraprecise optical clocks and trapping experiments with the $^{3}P_{2}$ fermionic isotopes. The resulting natural widths of the $^{3}P_{0}\ensuremath{-}^{1}S_{0}$ clock transition are $0.44\phantom{\rule{0.3em}{0ex}}\text{mHz}$ for $^{25}\mathrm{Mg}$, $2.2\phantom{\rule{0.3em}{0ex}}\text{mHz}$ for $^{43}\mathrm{Ca}$, $7.6\phantom{\rule{0.3em}{0ex}}\text{mHz}$ for $^{87}\mathrm{Sr}$, $43.5\phantom{\rule{0.3em}{0ex}}\text{mHz}$ for $^{171}\mathrm{Yb}$, and $38.5\phantom{\rule{0.3em}{0ex}}\text{mHz}$ for $^{173}\mathrm{Yb}$. Compared to the bosonic isotopes, the lifetime of the $^{3}P_{2}$ states in fermionic isotopes is noticeably shortened by the hyperfine quenching but still remains long enough for trapping experiments.

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We report the first experimental determination of the hyperfine quenching rate of the $6{s}^{2}\text{ }^{1}{S}_{0}(F=1/2)\ensuremath{-}6s6p\text{ }^{3}{P}_{0}(F=1/2)$ transition in $^{171}\mathrm{Yb}$ with nuclear spin $I=1/2$. This rate determines the natural linewidth and the Rabi frequency of the clock transition of a Yb optical frequency standard. Our technique involves spectrally resolved fluorescence decay measurements of the lowest lying $^{3}{P}_{0,1}$ levels of neutral Yb atoms embedded in a solid Ne matrix. The solid Ne provides a simple way to trap a large number of atoms as well as an efficient mechanism for populating $^{3}{P}_{0}$. The decay rates in solid Ne are modified by medium effects including the index-of-refraction dependence. We find the $^{3}{P}_{0}$ hyperfine quenching rate to be $(4.42\ifmmode\pm\else\textpm\fi{}0.35)\ifmmode\times\else\texttimes\fi{}1{0}^{\ensuremath{-}2}\text{ }\text{ }{\mathrm{s}}^{\ensuremath{-}1}$ for free $^{171}\mathrm{Yb}$, which agrees with recent ab initio calculations.

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Hyperfine quenching of the metastable ^3P~0~,~2 states in divalent atoms (6 pages)

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Dynamic polarizabilities and triply magic trapping conditions for 5s2S01→5s5p3P0,2 transitions of Cd atoms

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The dynamic electric dipole polarizabilities of the $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}$, $5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$, and $5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ states for Cd atoms are calculated using the relativistic configuration interaction plus many-body perturbation theory method. The magic wavelengths for the $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$ and $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ transitions within a range of 300--500 nm are identified. The possibility of achieving triple magic trapping for the transitions $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$ and $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ is investigated. It is found that no common magic wavelength could be identified for achieving triple magic trapping with the linearly polarized light. However, if the degree of ellipticity is between 0.358 and 1, the triple magic trapping can be achieved at 419.88 nm for the $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ $({M}_{i}=\ifmmode\pm\else\textpm\fi{}2)$ and $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$ transitions.

arXiv:2403.05898•Physical Review A•Mar 27, 2024•7 citations

Hyperfine Structure in the $^{87}$Rb$_{2}$ $1_{g}$ State Below $5^{2}S+5^{2}P_{1/2}$

T. H. Bergeman, Eite Tiesinga, Paul S. Julienne +2 more

APS•Jun 1, 2012•1 citation
Hyperfine quenching rates of nsnp 3P0−ns2 1S0nsnp\,^3P_0-ns^2\,^1S_0nsnp3P0​−ns21S0​ transition in 25^{25}25Mg, 87^{87}87Sr and 113^{113}113Cd
Hyperfine quenching rates of the lowest-energy metastable 3P0^{3}P_{0}3P0​ and 3P2^{3}P_{2}3P2​ states of Mg, Ca, Sr, and Yb atoms are computed. The calculations are carried out using ab initio relativistic many-body methods. The computed lifetimes may be useful for designing novel ultraprecise optical clocks and trapping experiments with the 3P2^{3}P_{2}3P2​ fermionic isotopes. The resulting natural widths of the $^{3}P_{0}\ensuremath{-}^{1}S_{0}$ clock transition are 0.44mHz0.44\phantom{\rule{0.3em}{0ex}}\text{mHz}0.44mHz for 25Mg^{25}\mathrm{Mg}25Mg, 2.2mHz2.2\phantom{\rule{0.3em}{0ex}}\text{mHz}2.2mHz for 43Ca^{43}\mathrm{Ca}43Ca, 7.6mHz7.6\phantom{\rule{0.3em}{0ex}}\text{mHz}7.6mHz for 87Sr^{87}\mathrm{Sr}87Sr, 43.5mHz43.5\phantom{\rule{0.3em}{0ex}}\text{mHz}43.5mHz for 171Yb^{171}\mathrm{Yb}171Yb, and 38.5mHz38.5\phantom{\rule{0.3em}{0ex}}\text{mHz}38.5mHz for 173Yb^{173}\mathrm{Yb}173Yb. Compared to the bosonic isotopes, the lifetime of the 3P2^{3}P_{2}3P2​ states in fermionic isotopes is noticeably shortened by the hyperfine quenching but still remains long enough for trapping experiments.
We report the first experimental determination of the hyperfine quenching rate of the $6{s}^{2}\text{ }^{1}{S}_{0}(F=1/2)\ensuremath{-}6s6p\text{ }^{3}{P}_{0}(F=1/2)$ transition in 171Yb^{171}\mathrm{Yb}171Yb with nuclear spin I=1/2I=1/2I=1/2. This rate determines the natural linewidth and the Rabi frequency of the clock transition of a Yb optical frequency standard. Our technique involves spectrally resolved fluorescence decay measurements of the lowest lying 3P0,1^{3}{P}_{0,1}3P0,1​ levels of neutral Yb atoms embedded in a solid Ne matrix. The solid Ne provides a simple way to trap a large number of atoms as well as an efficient mechanism for populating 3P0^{3}{P}_{0}3P0​. The decay rates in solid Ne are modified by medium effects including the index-of-refraction dependence. We find the 3P0^{3}{P}_{0}3P0​ hyperfine quenching rate to be $(4.42\ifmmode\pm\else\textpm\fi{}0.35)\ifmmode\times\else\texttimes\fi{}1{0}^{\ensuremath{-}2}\text{ }\text{ }{\mathrm{s}}^{\ensuremath{-}1}$ for free 171Yb^{171}\mathrm{Yb}171Yb, which agrees with recent ab initio calculations.
The dynamic electric dipole polarizabilities of the 5s21S05{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}5s21S0​, 5s5p3P05s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}5s5p3P0​, and 5s5p3P25s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}5s5p3P2​ states for Cd atoms are calculated using the relativistic configuration interaction plus many-body perturbation theory method. The magic wavelengths for the $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$ and $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ transitions within a range of 300--500 nm are identified. The possibility of achieving triple magic trapping for the transitions $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$ and $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ is investigated. It is found that no common magic wavelength could be identified for achieving triple magic trapping with the linearly polarized light. However, if the degree of ellipticity is between 0.358 and 1, the triple magic trapping can be achieved at 419.88 nm for the $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{2}$ $({M}_{i}=\ifmmode\pm\else\textpm\fi{}2)$ and $5{s}^{2}\phantom{\rule{0.16em}{0ex}}^{1}S_{0}\ensuremath{\rightarrow}5s5p\phantom{\rule{0.16em}{0ex}}^{3}P_{0}$ transitions.
Hyperfine Structure in the 87^{87}87Rb2_{2}2​ 1g1_{g}1g​ State Below 52S+52P1/25^{2}S+5^{2}P_{1/2}52S+52P1/2​