Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:1805.06878 · Physical Review A

Anisotropic light shift and magic polarization of the intercombination line of dysprosium atoms in a far-detuned dipole trap

Thomas Chalopin, Vasiliy Makhalov, Chayma Bouazza, Alexandre Evrard, Adam Barker, Maxence Lepers, Jean-François Wyart, Olivier Dulieu, Jean Dalibard, Raphael Lopes, Sylvain Nascimbène

Published Oct 22, 2018• 25 citations
arXivHTMLPDF

Abstract

We characterize the anisotropic differential ac-Stark shift for the Dy $626\phantom{\rule{3.33333pt}{0ex}}\mathrm{nm}$ intercombination transition, induced in a far-detuned $1070\phantom{\rule{3.33333pt}{0ex}}\mathrm{nm}$ optical dipole trap, and observe the existence of a ``magic polarization'' for which the polarizabilities of the ground and excited states are equal. From our measurements we extract both the scalar and tensorial components of the dynamic dipole polarizability for the excited state, ${\ensuremath{\alpha}}_{E}^{\text{s}}=188(12){\ensuremath{\alpha}}_{\text{0}}$ and ${\ensuremath{\alpha}}_{E}^{\text{t}}=34(12){\ensuremath{\alpha}}_{\text{0}}$, respectively, where ${\ensuremath{\alpha}}_{\text{0}}$ is the atomic unit for the electric polarizability. We also provide a theoretical model allowing us to predict the excited state polarizability and find qualitative agreement with our observations. Furthermore, we utilize our findings to optimize the efficiency of Doppler cooling of a trapped gas, by controlling the sign and magnitude of the inhomogeneous broadening of the optical transition. The resulting initial gain of the collisional rate allows us, after forced evaporation cooling, to produce a quasipure Bose-Einstein condensate of $^{162}\mathrm{Dy}$ with $3\ifmmode\times\else\texttimes\fi{}{10}^{4}$ atoms.

DOI
10.1103/physreva.98.040502

Related papers

Anisotropic polarizability of Dy at 532 nm on the intercombination transition

Damien Bloch, Britton Hofer, Sam R. Cohen +3 more

We report experimental measurements of the dynamical polarizability of dysprosium, at a wavelength of 532 nm. We measure all three components (scalar, vector, and tensor) of the anisotropic polarizability for the ground and the excited manifolds of the intercombination transition of Dy at 626 nm. The apparatus on which the measurements are performed is presented. We obtain with this setup imaging of single Dy atoms with fidelity above 99% and losses below 2.5% induced by imaging. We then describe the methods used to extract the polarizability. In particular, we combine a measurement of trap frequency and trap depth on single atoms in optical tweezers, allowing us to obtain a measurement of the ground-state polarizability free of errors in trap waist calibration. The obtained values give a magic condition between two Zeeman states in the ground and excited manifolds, which is used to image single atoms in optical tweezer arrays. The scalar polarizability of the ground state is in disagreement with theoretical expectations, calling for future investigations to resolve the discrepancy.

arXiv:2404.10480•Physical Review A•Sep 5, 2024•7 citations

Angle-Dependent Magic Optical Trap for the 6S1/2↔nP3/2 Rydberg Transition of Cesium Atoms

Jiandong Bai, Xin Wang, Xiaokai Hou +2 more

The existence of an anisotropic tensor part of atomic states with an angular momentum greater than 1/2 causes their dynamic polarizabilities to be very sensitive to the polarization direction of the laser field. Therefore, the magic wavelength of the transition between two atomic states also depends on the polarization angle between the quantized axis and the polarization vector. We perform a calculation of the magic conditions of the 6S1/2↔nP3/2 (n = 50–90) Rydberg transition of cesium atoms by introducing an auxiliary electric diople transition connected to the target Rydberg state and a low-excited state. The magic condition is determined by the intersection of dynamic polarizabilities of the 6S1/2 ground state and the nP3/2 Rydberg state. The dynamic polarizability is calculated by using the sum-over-states method. Furthermore, we analyze the dependence of magic detuning on the polarization angle for a linearly polarized trapping laser and establish the relationship between magic detuning and a principal quantum number of the Rydberg state at the magic angle. The magic optical dipole trap can confine the ground-state and Rydberg-state atoms simultaneously, and the differential light shift in the 6S1/2↔nP3/2 transition can be canceled under the magic condition. It is of great significance for the application of long-lifetime high-repetition-rate accurate manipulation of Rydberg atoms on high-fidelity entanglement and quantum logic gate operation.

Photonics•Apr 28, 2022•6 citations

Optical trapping of ultracold dysprosium atoms: transition probabilities, dynamic dipole polarizabilities and van der Waals C 6 coefficients

H Li, Jean-François Wyart, Olivier Dulieu +2 more

Abstract The efficiency of the optical trapping of ultracold atoms depends on the atomic dynamic dipole polarizability governing the atom-field interaction. In this article, we have calculated the real and imaginary parts of the dynamic dipole polarizability of dysprosium in the ground and first excited levels. Due to the high electronic angular momentum of those two states, the polarizabilities possess scalar, vector and tensor contributions that we have computed, on a wide range of trapping wavelengths, using the sum-over-state formula. Using the same formalism, we have also calculated the C 6 coefficients characterizing the van der Waals interaction between two dysprosium atoms in the two lowest levels. We have computed the energies of excited states and the transition probabilities appearing in the sums, using a combination of ab initio and least-square-fitting techniques provided by the Cowan codes and extended in our group. Regarding the real part of the polarizability, for field frequencies far from atomic resonances, the vector and tensor contributions are two-orders-of-magnitude smaller than the scalar contribution, whereas for the imaginary part, the vector and tensor contributions represent a noticeable fraction of the scalar contribution. Finally, our anisotropic C 6 coefficients are much smaller than those published in the literature.

arXiv:1607.05628•Journal of Physics B Atomic Molecular and Optical Physics•Dec 15, 2016•46 citations

Magic Polarization for Optical Trapping of Atoms without Stark-Induced Dephasing

Huidong Kim, Hyok Sang Han, D. Cho

We demonstrate that the differential ac-Stark shift of a Zeeman-sensitive ground hyperfine transition in an optical trap can be eliminated by using properly polarized trapping light. We use the vector polarizability of an alkali-metal atom to produce a polarization-dependent ac-Stark shift that resembles a Zeeman shift. We study a transition from the $|2{S}_{1/2},F=2,{m}_{F}=\ensuremath{-}2⟩$ to the $|2{S}_{1/2},F=1,{m}_{F}=\ensuremath{-}1⟩$ state of $^{7}\mathrm{Li}$ to observe $0.59\ifmmode\pm\else\textpm\fi{}0.02\text{ }\text{ }\mathrm{Hz}$ linewidth with interrogation time of 2 s and $0.82\ifmmode\pm\else\textpm\fi{}0.06\text{ }\text{ }\mathrm{s}$ coherence time of a superposition state. Implications of the narrow linewidth and the long coherence time for precision spectroscopy and quantum information processing using atoms in an optical lattice are discussed.

arXiv:1311.1290•Physical Review Letters•Dec 11, 2013•34 citations

Determination of the ground-state polarizability of Dy 162 near 530 nm

Alexandre Journeaux, Maxime Lecomte, Julie Veschambre +3 more

Open-shell lanthanide atoms, and dysprosium in particular, combine a large ground-state angular momentum with dense electronic spectra, making their dynamical polarizability strongly dependent on wavelength and internal state, and therefore challenging to calculate and characterize experimentally. This issue has become especially relevant with the recent development of single-atom trapping of dysprosium in optical-tweezer arrays, where precise knowledge of the polarizability is needed to design optimized trapping architectures. Here, we exploit the strong spin-dependent light shift near the $J'=J-1$ intercombination line at 530.306 nm to determine the background scalar and vector polarizabilities of $^{162}$Dy in its ground state near this wavelength. Our measurements quantitatively agree with atomic-structure calculations and provide new insight into the contributions of nearby transitions in a spectral region relevant to emerging dysprosium tweezer platforms.

arXiv:2604.03177•Physical Review A•Jul 15, 2026•0 citations

Dynamic polarizabilities and magic wavelengths for dysprosium

V. A. Dzuba, V. V. Flambaum, Benjamin Lev

We theoretically study dynamic scalar polarizabilities of the ground and select long-lived excited states of dysprosium, a highly magnetic atom recently laser cooled and trapped. We demonstrate that there is a set of magic wavelengths of the unpolarized lattice laser field for each pair of states, which includes the ground state and one of these excited states. At these wavelengths, the energy shift due to laser field is the same for both states, which can be useful for resolved sideband cooling on narrow transitions and precision spectroscopy. We present an analytical formula that, near resonances, allows for the determination of approximate values of the magic wavelengths without calculating the dynamic polarizabilities of the excited states.

arXiv:1011.4738•Physical Review A•Mar 4, 2011•39 citations
We characterize the anisotropic differential ac-Stark shift for the Dy 626nm626\phantom{\rule{3.33333pt}{0ex}}\mathrm{nm}626nm intercombination transition, induced in a far-detuned 1070nm1070\phantom{\rule{3.33333pt}{0ex}}\mathrm{nm}1070nm optical dipole trap, and observe the existence of a ``magic polarization'' for which the polarizabilities of the ground and excited states are equal. From our measurements we extract both the scalar and tensorial components of the dynamic dipole polarizability for the excited state, \ensuremathαEs=188(12)\ensuremathα0{\ensuremath{\alpha}}_{E}^{\text{s}}=188(12){\ensuremath{\alpha}}_{\text{0}}\ensuremathαEs​=188(12)\ensuremathα0​ and \ensuremathαEt=34(12)\ensuremathα0{\ensuremath{\alpha}}_{E}^{\text{t}}=34(12){\ensuremath{\alpha}}_{\text{0}}\ensuremathαEt​=34(12)\ensuremathα0​, respectively, where \ensuremathα0{\ensuremath{\alpha}}_{\text{0}}\ensuremathα0​ is the atomic unit for the electric polarizability. We also provide a theoretical model allowing us to predict the excited state polarizability and find qualitative agreement with our observations. Furthermore, we utilize our findings to optimize the efficiency of Doppler cooling of a trapped gas, by controlling the sign and magnitude of the inhomogeneous broadening of the optical transition. The resulting initial gain of the collisional rate allows us, after forced evaporation cooling, to produce a quasipure Bose-Einstein condensate of 162Dy^{162}\mathrm{Dy}162Dy with 3\ifmmode×\else\texttimes\fi1043\ifmmode\times\else\texttimes\fi{}{10}^{4}3\ifmmode×\else\texttimes\fi104 atoms.
We report experimental measurements of the dynamical polarizability of dysprosium, at a wavelength of 532 nm. We measure all three components (scalar, vector, and tensor) of the anisotropic polarizability for the ground and the excited manifolds of the intercombination transition of Dy at 626 nm. The apparatus on which the measurements are performed is presented. We obtain with this setup imaging of single Dy atoms with fidelity above 99% and losses below 2.5% induced by imaging. We then describe the methods used to extract the polarizability. In particular, we combine a measurement of trap frequency and trap depth on single atoms in optical tweezers, allowing us to obtain a measurement of the ground-state polarizability free of errors in trap waist calibration. The obtained values give a magic condition between two Zeeman states in the ground and excited manifolds, which is used to image single atoms in optical tweezer arrays. The scalar polarizability of the ground state is in disagreement with theoretical expectations, calling for future investigations to resolve the discrepancy.
The existence of an anisotropic tensor part of atomic states with an angular momentum greater than 1/2 causes their dynamic polarizabilities to be very sensitive to the polarization direction of the laser field. Therefore, the magic wavelength of the transition between two atomic states also depends on the polarization angle between the quantized axis and the polarization vector. We perform a calculation of the magic conditions of the 6S1/2↔nP3/2 (n = 50–90) Rydberg transition of cesium atoms by introducing an auxiliary electric diople transition connected to the target Rydberg state and a low-excited state. The magic condition is determined by the intersection of dynamic polarizabilities of the 6S1/2 ground state and the nP3/2 Rydberg state. The dynamic polarizability is calculated by using the sum-over-states method. Furthermore, we analyze the dependence of magic detuning on the polarization angle for a linearly polarized trapping laser and establish the relationship between magic detuning and a principal quantum number of the Rydberg state at the magic angle. The magic optical dipole trap can confine the ground-state and Rydberg-state atoms simultaneously, and the differential light shift in the 6S1/2↔nP3/2 transition can be canceled under the magic condition. It is of great significance for the application of long-lifetime high-repetition-rate accurate manipulation of Rydberg atoms on high-fidelity entanglement and quantum logic gate operation.
Abstract The efficiency of the optical trapping of ultracold atoms depends on the atomic dynamic dipole polarizability governing the atom-field interaction. In this article, we have calculated the real and imaginary parts of the dynamic dipole polarizability of dysprosium in the ground and first excited levels. Due to the high electronic angular momentum of those two states, the polarizabilities possess scalar, vector and tensor contributions that we have computed, on a wide range of trapping wavelengths, using the sum-over-state formula. Using the same formalism, we have also calculated the C 6 coefficients characterizing the van der Waals interaction between two dysprosium atoms in the two lowest levels. We have computed the energies of excited states and the transition probabilities appearing in the sums, using a combination of ab initio and least-square-fitting techniques provided by the Cowan codes and extended in our group. Regarding the real part of the polarizability, for field frequencies far from atomic resonances, the vector and tensor contributions are two-orders-of-magnitude smaller than the scalar contribution, whereas for the imaginary part, the vector and tensor contributions represent a noticeable fraction of the scalar contribution. Finally, our anisotropic C 6 coefficients are much smaller than those published in the literature.
We demonstrate that the differential ac-Stark shift of a Zeeman-sensitive ground hyperfine transition in an optical trap can be eliminated by using properly polarized trapping light. We use the vector polarizability of an alkali-metal atom to produce a polarization-dependent ac-Stark shift that resembles a Zeeman shift. We study a transition from the $|2{S}_{1/2},F=2,{m}_{F}=\ensuremath{-}2⟩$ to the $|2{S}_{1/2},F=1,{m}_{F}=\ensuremath{-}1⟩$ state of 7Li^{7}\mathrm{Li}7Li to observe $0.59\ifmmode\pm\else\textpm\fi{}0.02\text{ }\text{ }\mathrm{Hz}$ linewidth with interrogation time of 2 s and $0.82\ifmmode\pm\else\textpm\fi{}0.06\text{ }\text{ }\mathrm{s}$ coherence time of a superposition state. Implications of the narrow linewidth and the long coherence time for precision spectroscopy and quantum information processing using atoms in an optical lattice are discussed.
Open-shell lanthanide atoms, and dysprosium in particular, combine a large ground-state angular momentum with dense electronic spectra, making their dynamical polarizability strongly dependent on wavelength and internal state, and therefore challenging to calculate and characterize experimentally. This issue has become especially relevant with the recent development of single-atom trapping of dysprosium in optical-tweezer arrays, where precise knowledge of the polarizability is needed to design optimized trapping architectures. Here, we exploit the strong spin-dependent light shift near the J′=J−1J'=J-1J′=J−1 intercombination line at 530.306 nm to determine the background scalar and vector polarizabilities of 162^{162}162Dy in its ground state near this wavelength. Our measurements quantitatively agree with atomic-structure calculations and provide new insight into the contributions of nearby transitions in a spectral region relevant to emerging dysprosium tweezer platforms.
We theoretically study dynamic scalar polarizabilities of the ground and select long-lived excited states of dysprosium, a highly magnetic atom recently laser cooled and trapped. We demonstrate that there is a set of magic wavelengths of the unpolarized lattice laser field for each pair of states, which includes the ground state and one of these excited states. At these wavelengths, the energy shift due to laser field is the same for both states, which can be useful for resolved sideband cooling on narrow transitions and precision spectroscopy. We present an analytical formula that, near resonances, allows for the determination of approximate values of the magic wavelengths without calculating the dynamic polarizabilities of the excited states.