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arXiv:1304.3326 · Physical Review A

Hyperfine structure of laser-cooling transitions in fermionic erbium-167

Albert Frisch, K. Aikawa, Michael F. Mark, Francesca Ferlaino, E. Berseneva, Svetlana Kotochigova

Published Sep 13, 2013• 36 citations
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Abstract

We have measured and analyzed the hyperfine structure of two lines, one at 583 nm and one at 401 nm, of the only stable fermionic isotope of atomic erbium as well as determined its isotope shift relative to the four most-abundant bosonic isotopes. Our work focuses on the $J\ensuremath{\rightarrow}J+1$ laser cooling transitions from the $[\text{Xe}]4{f}^{12}6{s}^{2}{(}^{3}{H}_{6})$ ground state to two levels of the excited $[\text{Xe}]4{f}^{12}6s6p$ configuration, which are of major interest for experiments on quantum degenerate dipolar Fermi gases. From a fit to the observed spectra of the strong optical transition at 401 nm we find that the magnetic dipole and electric quadrupole hyperfine constants for the excited state are ${A}_{e}/h=\ensuremath{-}100.1(3)\phantom{\rule{0.28em}{0ex}}\mathrm{MHz}$ and ${B}_{e}/h=\ensuremath{-}3079(30)\phantom{\rule{0.28em}{0ex}}\mathrm{MHz}$, respectively. The hyperfine spectrum of the narrow transition at 583 nm, was previously observed and accurate ${A}_{e}$ and ${B}_{e}$ coefficients are available. A simulated spectrum based on these coefficients agrees well with our measurements. We have also determined the hyperfine constants using relativistic configuration-interaction ab initio calculations. The agreement between the ab initio and fitted data for the ground state is better than 0.1%, while for the two excited states the agreement is 1% and 11% for the ${A}_{e}$ and ${B}_{e}$ constants, respectively.

DOI
10.1103/physreva.88.032508

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Laser cooling of neutral atoms or positive ions is today routinely employed in numerous experiments. Negative ions, in contrast, have distinct characteristics which hamper the application of lasers for cooling. But in 1999, the discovery of the unique bound–bound electric dipole transition in the negative osmium ion provided the motivation for a first cooling attempt. This thesis presents the first milestones toward the ultimate goal of laser cooling negative osmium, including high-resolution laser spectroscopy of the relevant bound–bound E1 transition. Its frequency – between the ground 4F9/2 and the 6DJe1 (bound) excited states – was determined to be 257.831190(35) THz in 192Os-, in agreement\nwith a previous measurement, but two orders of magnitude more precise. The determination of the resonant cross-section implicitly provided the corresponding Einstein A coefficient, which was found to be A ~ 330 s-1. Furthermore, the isotope shift of the E1 transition and the hyperfine structure constants of the ground and excited state were obtained, for the first time, from the analysis of the spectra of all naturally abundant isotopes. The hyperfine structure revealed the heretofore unknown total angular momentum of the excited state to be Je1 = 9/2. Finally, laser spectroscopy in an external magnetic field confirmed the expected line splitting for Os- due to the Zeeman effect. Based on all these experimental results the prospect of laser cooling negative osmium is reviewed.

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Physical Review Letters•Feb 18, 2010•37 citations
We have measured and analyzed the hyperfine structure of two lines, one at 583 nm and one at 401 nm, of the only stable fermionic isotope of atomic erbium as well as determined its isotope shift relative to the four most-abundant bosonic isotopes. Our work focuses on the J\ensuremath→J+1J\ensuremath{\rightarrow}J+1J\ensuremath→J+1 laser cooling transitions from the [Xe]4f126s2(3H6)[\text{Xe}]4{f}^{12}6{s}^{2}{(}^{3}{H}_{6})[Xe]4f126s2(3H6​) ground state to two levels of the excited [Xe]4f126s6p[\text{Xe}]4{f}^{12}6s6p[Xe]4f126s6p configuration, which are of major interest for experiments on quantum degenerate dipolar Fermi gases. From a fit to the observed spectra of the strong optical transition at 401 nm we find that the magnetic dipole and electric quadrupole hyperfine constants for the excited state are Ae/h=\ensuremath−100.1(3)MHz{A}_{e}/h=\ensuremath{-}100.1(3)\phantom{\rule{0.28em}{0ex}}\mathrm{MHz}Ae​/h=\ensuremath−100.1(3)MHz and Be/h=\ensuremath−3079(30)MHz{B}_{e}/h=\ensuremath{-}3079(30)\phantom{\rule{0.28em}{0ex}}\mathrm{MHz}Be​/h=\ensuremath−3079(30)MHz, respectively. The hyperfine spectrum of the narrow transition at 583 nm, was previously observed and accurate Ae{A}_{e}Ae​ and Be{B}_{e}Be​ coefficients are available. A simulated spectrum based on these coefficients agrees well with our measurements. We have also determined the hyperfine constants using relativistic configuration-interaction ab initio calculations. The agreement between the ab initio and fitted data for the ground state is better than 0.1%, while for the two excited states the agreement is 1% and 11% for the Ae{A}_{e}Ae​ and Be{B}_{e}Be​ constants, respectively.
We report on the measurement of the isotope shifts of the 3d74sa5F5–3d74pz5G6o3{d}^{7}4s\phantom{\rule{0.28em}{0ex}}a\phantom{\rule{0.28em}{0ex}}{}^{5}{F}_{5}\text{--}3{d}^{7}4p\phantom{\rule{0.28em}{0ex}}z\phantom{\rule{0.28em}{0ex}}{}^{5}{G}_{6}^{o}3d74sa5F5​–3d74pz5G6o​ Fe i line at 358 nm between all four stable isotopes 54Fe,56Fe,57Fe^{54}\text{Fe},\phantom{\rule{0.16em}{0ex}}^{56}\text{Fe},\phantom{\rule{0.16em}{0ex}}^{57}\text{Fe}54Fe,56Fe,57Fe, and 58Fe^{58}\text{Fe}58Fe, as well as the hyperfine structure of that line for 57Fe^{57}\text{Fe}57Fe, the only stable isotope having a nonzero nuclear spin. This line is of primary importance for laser-cooling applications. In addition, an experimental value of the field and specific mass shift coefficients of the transition is reported as well as the hyperfine structure magnetic dipole coupling constant AAA of the transition excited state in 57Fe^{57}\text{Fe}57Fe, namely A(3d74pz5G6o)=31.241(48)A(3{d}^{7}4p\phantom{\rule{0.28em}{0ex}}z\phantom{\rule{0.28em}{0ex}}{}^{5}{G}_{6}^{o})=31.241(48)A(3d74pz5G6o​)=31.241(48) MHz. The measurements were carried out by means of laser-induced fluorescence spectroscopy performed on an isotope-enriched iron atomic beam. All measured frequency shifts are reported with relative uncertainties below one third percent.
High-Resolution Spectroscopy of 173^{173}173Yb+^{+}+ Ions
Compared to other stable isotopes of Yb+\rm{Yb}^+Yb+, 173Yb+^{173}\rm{Yb}^+173Yb+ has a richer hyperfine structure, which leads to more favorable clock transitions, spectroscopic techniques for probing new physics, and more sophisticated quantum computing architectures. However, to date, its electronic spectrum remains poorly characterized. Here, we report on efficient laser cooling, state preparation, and detection of a single trapped 173Yb+^{173}\rm{Yb}^+173Yb+ ion. The previously unobserved 2 ⁣S1/2→2 ⁣D3/2^2\!S_{1/2} \rightarrow {}^2\!D_{3/2}2S1/2​→2D3/2​ electric quadrupole transition at 436 nm is coherently excited, and the isotope shift between 171Yb+^{171}\rm{Yb}^+171Yb+ and 173Yb+^{173}\rm{Yb}^+173Yb+ on this transition is determined with an uncertainty of 1.4 Hz. Using microwave spectroscopy, we resolve the hyperfine structure (HFS) of the 2 ⁣D3/2{}^2\!D_{3/2}2D3/2​ state with a relative uncertainty below 10−810^{-8}10−8. From the HFS measurement data, we infer for 173{}^{173}173Yb a nuclear magnetic octupole moment Ω=−0.062(8) (b×μN)Ω= -0.062(8)\,({\rm b} \times μ_N)Ω=−0.062(8)(b×μN​) with uncertainty reduced by more than 2 orders of magnitude compared to previous studies. The data also allow us to determine hyperfine anomalies for the 2 ⁣S1/2{}^2\!S_{1/2}2S1/2​ and 2 ⁣D3/2{}^2\!D_{3/2}2D3/2​ states.
Full text: It has been shown recently that Yb and Er atoms from the lanthanides group can be efficiently laser-cooled using strong transitions near 400 nm. Degenerate Fermi gases of ytterbium have been also recently demonstrated using laser-cooling based technic. Our goal was to investigate the possibility of laser cooling of Tm atom. Among other lanthanides, thulium possesses relatively simple level structure.Moreover, it has only one stable isotope {sup 169}Tm with a nuclear spin of I = 1/2 which makes possible to use schemes for sub-Doppler cooling. Laser-cooled thulium is a favorable candidate for optical clocks applications, since the forbidden transition between the fine structure sublevels (J{sub g} 5=2) - (J'{sub g} = 7/2) of the ground state 4f{sup 13}6s{sup 2} ({lambda} = 1.14 micron) has a spectral width of approximately 1 Hz. The collisional shift of such kind of transitions in lanthanides is suppressed because of the outer closed 6s{sup 2} shell, which allows for precision spectroscopy in a dense atomic cloud. We studied two candidates for cooling transitions from the ground state 4f{sup 13}6s{sup 2} (J{sub g} 7/2) to the states 4f{sup 12}({sup 3}H{sub 5})5d{sub 3/2}6s{sup 2} (J{sub e} = 9/2) at 410.6 nm and 4f{sup 12}({sup 3}F{sub 4})5d{sub 5/2}6s{sup 2} (J{sub e} = 9/2) at 420.4 nm. By means of saturation absorption spectroscopy, we measured the hyperfine structure and rates of these transitions. We evaluated the life times of appropriate excited levels as 15.9(8) ns and 48(6) ns, respectively. Decay rates from these levels to neighboring opposite-parity levels were evaluated by means of Hartree-Fock calculations. The fraction of atoms which do not return to the ground state is about 10{sup -5} and 5 {center_dot} 10{sup -4} for the 410.6 nm and 420.4 nm transitions respectively. We conclude that the strong transition at 410.6 nm with relative slow leakage rate can be used for the efficient cooling of Tm I. We also measured hyperfine structure of two nearby transitions from the ground state to the states 4f{sup 13}({sup 2}F{sub 7/2})6s6p({sup 1}P{sub 1}) (J{sub e} 5/2) at 409.4 nm and 4f{sup 12}({sup 3}F{sub 4})5d{sub 5/2}6s{sup 2} (J{sub e} = 7/2) at 418.9 nm, which can be used for {lambda}-type excitation of {lambda} = 1.14 {mu}m transition. (author)
Laser cooling of neutral atoms or positive ions is today routinely employed in numerous experiments. Negative ions, in contrast, have distinct characteristics which hamper the application of lasers for cooling. But in 1999, the discovery of the unique bound–bound electric dipole transition in the negative osmium ion provided the motivation for a first cooling attempt. This thesis presents the first milestones toward the ultimate goal of laser cooling negative osmium, including high-resolution laser spectroscopy of the relevant bound–bound E1 transition. Its frequency – between the ground 4F9/2 and the 6DJe1 (bound) excited states – was determined to be 257.831190(35) THz in 192Os-, in agreement\nwith a previous measurement, but two orders of magnitude more precise. The determination of the resonant cross-section implicitly provided the corresponding Einstein A coefficient, which was found to be A ~ 330 s-1. Furthermore, the isotope shift of the E1 transition and the hyperfine structure constants of the ground and excited state were obtained, for the first time, from the analysis of the spectra of all naturally abundant isotopes. The hyperfine structure revealed the heretofore unknown total angular momentum of the excited state to be Je1 = 9/2. Finally, laser spectroscopy in an external magnetic field confirmed the expected line splitting for Os- due to the Zeeman effect. Based on all these experimental results the prospect of laser cooling negative osmium is reviewed.
We present the first measurements of the [Xe]4f75d16s6p$\;^{11}{F_J}$11FJ excited state hyperfine coefficients and isotope shifts of spin-forbidden transitions of atomic gadolinium (Gd) at 726 and 743 nm in a hollow cathode gas discharge. In addition, we performed a King Plot analysis to determine specific mass shift and field shift constants for these lines. Moreover, we observed King Plot nonlinearity for the 743 nm transition, which is an effect recently proposed to aid in searches for hypothetical new light bosons. Spectroscopic results obtained from this study will facilitate the development of more efficient isotope separation techniques, enable narrowband laser cooling of Gd for novel dipolar physics investigations, and foster technological advances in high precision atomic clocks and quantum enhanced metrology.
We have investigated the hyperfine structure of the transition between the 5d{7}6s{2} {4}F{9/2}{e} ground state and the 5d{6}6s{2}6p {6}D{J}{o} excited state in the negative osmium ion by high-resolution collinear laser spectroscopy. This transition is unique because it is the only known electric-dipole transition in atomic anions and might be amenable to laser cooling. From the observed hyperfine structure in 187Os- and 189Os- the yet unknown total angular momentum of the bound excited state was found to be J=9/2. The hyperfine structure constants of the {4}F{9/2}{e} ground state and the {6}D{9/2}{o} excited state were determined experimentally and compared to multiconfiguration Dirac-Fock calculations. Using the knowledge of the ground and excited state angular momenta, the full energy level diagram of 192Os- in an external magnetic field was calculated, revealing possible laser cooling transitions.