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A magic wavelength optical dipole trap for high-precision spectroscopy of utracold metastable helium

Robert J. Rengelink

Published Dec 10, 2018• 0 citations
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A simple 2 W continuous-wave laser system for trapping ultracold metastable helium atoms at the 319.8 nm magic wavelength

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High-precision spectroscopy on the $$2 \ ^3 S \rightarrow 2 \ ^1 S$$ transition is possible in ultracold optically trapped helium, but the accuracy is limited by the ac-Stark shift induced by the optical dipole trap. To overcome this problem, we have built a trapping laser system at the predicted magic wavelength of 319.8 nm. Our system is based on frequency conversion using commercially available components and produces over 2 W of power at this wavelength. With this system, we show trapping of ultracold atoms, both thermal (~0.2 μk) and in a Bose–Einstein condensate, with a trap lifetime of several seconds, mainly limited by off-resonant scattering .

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A large-scale full-configuration-interaction calculation based on the Dirac-Coulomb-Breit (DCB) Hamiltonian is performed for the $2{\phantom{\rule{0.16em}{0ex}}}^{1}{S}_{0}$ and $2{\phantom{\rule{0.16em}{0ex}}}^{3}{S}_{1}$ states of helium. The operators of the normal and specific mass shifts are directly included in the DCB framework to take the finite nuclear mass correction into account. High-accuracy energies and matrix elements involved $n$ (the main quantum number) up to 13 are obtained from one diagonalization of Hamiltonian. The dynamic dipole polarizabilities are calculated by using the sum rule of intermediate states, and a series of magic wavelengths with QED and hyperfine effects included for the $2{\phantom{\rule{0.16em}{0ex}}}^{3}{S}_{1}\ensuremath{\rightarrow}2{\phantom{\rule{0.16em}{0ex}}}^{1}{S}_{0}$ transition of helium are identified. In addition, the high-order ac Stark shift determined by the dynamic hyperpolarizabilities at the magic wavelengths are also evaluated. Since the most promising magic wavelength for application in experiment is 319.8 nm, the high-accuracy magic wavelength of 319.815 3(6) nm of $^{4}\mathrm{He}$ is in good agreement with the recent measurement value of 319.815 92(15) nm [R. J. Rengelink et al., arXiv:1804.06693], and the present magic wavelength of 319.830 2(7) nm for $^{3}\mathrm{He}$ would provide theoretical support for experimentally designing an optical dipole trap to precisely determine the nuclear charge radius of helium in the future.

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Magic wavelengths with QED correction for the 23 S 1 → 23 P J transitions of helium-4

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A series of magic wavelengths for the 23S1 → 23PJ (J = 0, 1, 2) transitions in helium is determined with high precision using the relativistic configuration interaction combined with the radiative potential method. The calculation explicitly incorporates relativistic, finite nuclear mass, and quantum electrodynamic corrections through the inclusion of mass shift and radiative potential operators into the Dirac-Coulomb-Breit Hamiltonian. The resulting magic wavelengths lie entirely within the visible spectrum (400-700 nm) and converge to seven significant digits, making them directly accessible for experimental verification. These accurate predictions serve as benchmarks for testing atomic structure theory and support the development of state-insensitive optical trapping schemes in precision spectroscopy.

The Journal of Chemical Physics•Mar 17, 2026•0 citations
High-precision spectroscopy on the 2 3S→2 1S2 \ ^3 S \rightarrow 2 \ ^1 S2 3S→2 1S transition is possible in ultracold optically trapped helium, but the accuracy is limited by the ac-Stark shift induced by the optical dipole trap. To overcome this problem, we have built a trapping laser system at the predicted magic wavelength of 319.8 nm. Our system is based on frequency conversion using commercially available components and produces over 2 W of power at this wavelength. With this system, we show trapping of ultracold atoms, both thermal (~0.2 μk) and in a Bose–Einstein condensate, with a trap lifetime of several seconds, mainly limited by off-resonant scattering .
A large-scale full-configuration-interaction calculation based on the Dirac-Coulomb-Breit (DCB) Hamiltonian is performed for the 21S02{\phantom{\rule{0.16em}{0ex}}}^{1}{S}_{0}21S0​ and 23S12{\phantom{\rule{0.16em}{0ex}}}^{3}{S}_{1}23S1​ states of helium. The operators of the normal and specific mass shifts are directly included in the DCB framework to take the finite nuclear mass correction into account. High-accuracy energies and matrix elements involved nnn (the main quantum number) up to 13 are obtained from one diagonalization of Hamiltonian. The dynamic dipole polarizabilities are calculated by using the sum rule of intermediate states, and a series of magic wavelengths with QED and hyperfine effects included for the $2{\phantom{\rule{0.16em}{0ex}}}^{3}{S}_{1}\ensuremath{\rightarrow}2{\phantom{\rule{0.16em}{0ex}}}^{1}{S}_{0}$ transition of helium are identified. In addition, the high-order ac Stark shift determined by the dynamic hyperpolarizabilities at the magic wavelengths are also evaluated. Since the most promising magic wavelength for application in experiment is 319.8 nm, the high-accuracy magic wavelength of 319.815 3(6) nm of 4He^{4}\mathrm{He}4He is in good agreement with the recent measurement value of 319.815 92(15) nm [R. J. Rengelink et al., arXiv:1804.06693], and the present magic wavelength of 319.830 2(7) nm for 3He^{3}\mathrm{He}3He would provide theoretical support for experimentally designing an optical dipole trap to precisely determine the nuclear charge radius of helium in the future.
A series of magic wavelengths for the 23S1 → 23PJ (J = 0, 1, 2) transitions in helium is determined with high precision using the relativistic configuration interaction combined with the radiative potential method. The calculation explicitly incorporates relativistic, finite nuclear mass, and quantum electrodynamic corrections through the inclusion of mass shift and radiative potential operators into the Dirac-Coulomb-Breit Hamiltonian. The resulting magic wavelengths lie entirely within the visible spectrum (400-700 nm) and converge to seven significant digits, making them directly accessible for experimental verification. These accurate predictions serve as benchmarks for testing atomic structure theory and support the development of state-insensitive optical trapping schemes in precision spectroscopy.