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Acta Physica Sinica

Experimental research on loading strontium bosons into the optical lattice operating at the “magic” wavelength

Tian Xiao, Wang Ye-Bing, Lu Ben-Quan, Liu Hui, Qinfang Xu, Jie Ren, Yin Mo-Juan, Kong De-Huan, Chang Hong, Shougang Zhang

Published Jan 1, 2015• 0 citations
Publisher

Abstract

The optical lattice clock with neutral atoms occupies an outstanding position in the research field of atomic clocks, demonstrating the great potential of its performance (like the uncertainty and the stability). At present, the optical lattice clock has realized a 10-18 level of its uncertainty. In this paper, we present the realization of loading bosonic atoms 88Sr (strontium, alkaline-earth metals) into a one-dimensional (1D) optical lattice in our laboratory. The optical lattice where the atoms are trapped can make the energy level shift, called Stark shift. But there is the special optical lattice operating at the “magic” wavelength for clock transitions (5s2) 1S0-(5s5p) 3P0, which can make the same Stark light-shift for both of them, indicating a zero light-shift relative to the clock. In our experiment, Sr atoms are cooled in a two-stage cooling and its temperature can be as low as 2 μK. Then these cold atoms are confined in the Lamb-Dicke region by the lattice laser output from an amplified diode laser operating at the “magic” wavelength, 813 nm. Experimentally, it is straightforward to provide 850 mW of lattice power focused to a 38 μm beam radius. After the cold atoms have trapped in the optical lattice, the lifetime of atoms in 1D optical lattice is measured to be 270 ms. The temperature and the number are about 3.5 μK and 1.2×105 respectively. Besides, effects of the power of the lattice laser on both the number and temperature are analyzed. The number changes linearly with the laser power, while there is no obvious influence on the temperature by the power. This original and special approach for atoms trapped in the optical lattice can provide a long interrogation time for probing the clock transition. Furthermore, it may be the foundation for developing our optical lattice clock of strontium atoms.

DOI
10.7498/aps.64.130601

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State-of-the-art optical clocks based on neutral atoms have already surpassed the world's best microwave atomic clocks in both accuracy and stability, paving the way to high-precision measurements of elementary aspects of nature, like the search for the drift of fundamental constants or the application of relativistic geodesy.These clocks operate with ensembles trapped in an optical lattice.Normally, high-power trapping laser fields induce a large AC Stark shift on the clock's transition frequency, as the clock states have different polarizabilities.A key feature of lattice clocks is the magic wavelength, for which the atomic polarizabilities of the clock states are equal, therefore compensating a differential frequency shift on the clock transition.In the periodic potential of the optical lattice, the energy spectrum of motional states features a band structure, analogous to electrons in a crystalline structure well-known from solid state physics.Within this band structure, atoms can tunnel between adjacent lattice sites.As a consequence from tunneling motion, the clock transition experiences a frequency shift and a broadening, which becomes pronounced in the shallow lattice regime.This work presents the first demonstration of a 24 Mg optical lattice clock including the precise determination of the frequency of the clock transition, its magic wavelength and its second-order Zeeman shift.Furthermore, the effect of tunneling in an optical lattice for magnesium has been extensively studied via optical spectroscopy of Bloch bands and substantiated with theoretical models, that were initially developed for a strontium optical lattice clock.Measuring lattice light induced frequency shifts of the clock transition for various lattice wavelengths and intensities, yielded a value of the magic wavelength of the 1 S 0 → 3 P 0 clock transition in 24 Mg of 468.463(207) nm.This value is in well agreement with a recent theoretical calculation of 468.45(23) nm, using a refined atomic structure model.The experimental value for the magic wavelength was independently verified with optical spectroscopy of Bloch bands carried out on the clock transition.Here, the AC Stark modified band structure is directly probed by a single frequency scan of the carrier resonance, featuring an asymmetric line shape, that is strongly dependent on the lattice wavelength.This technique demonstrates a novel method for the determination of the magic wavelength and could also be applied to other atomic species.In bosonic isotopes of alkaline earth(-like) elements, like 24 Mg, optical dipole excitation of the spin-forbidden 1 S 0 → 3 P 0 clock transition can be enhanced, e.g. by applying an external magnetic field.While these bosons are insensitive to first-order Zeeman shifts, the second-order Zeeman effect displays a dominant contribution to the clock's error budget.In this thesis, the magnetic polarizability β is measured to be -206.6(2.0)MHz/T 2 , consistent with a theoretical calculation, and the clock transition frequency was found to be 655 058 646 691(101) kHz.

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The optical lattice clock with neutral atoms occupies an outstanding position in the research field of atomic clocks, demonstrating the great potential of its performance (like the uncertainty and the stability). At present, the optical lattice clock has realized a 10-18 level of its uncertainty. In this paper, we present the realization of loading bosonic atoms 88Sr (strontium, alkaline-earth metals) into a one-dimensional (1D) optical lattice in our laboratory. The optical lattice where the atoms are trapped can make the energy level shift, called Stark shift. But there is the special optical lattice operating at the “magic” wavelength for clock transitions (5s2) 1S0-(5s5p) 3P0, which can make the same Stark light-shift for both of them, indicating a zero light-shift relative to the clock. In our experiment, Sr atoms are cooled in a two-stage cooling and its temperature can be as low as 2 μK. Then these cold atoms are confined in the Lamb-Dicke region by the lattice laser output from an amplified diode laser operating at the “magic” wavelength, 813 nm. Experimentally, it is straightforward to provide 850 mW of lattice power focused to a 38 μm beam radius. After the cold atoms have trapped in the optical lattice, the lifetime of atoms in 1D optical lattice is measured to be 270 ms. The temperature and the number are about 3.5 μK and 1.2×105 respectively. Besides, effects of the power of the lattice laser on both the number and temperature are analyzed. The number changes linearly with the laser power, while there is no obvious influence on the temperature by the power. This original and special approach for atoms trapped in the optical lattice can provide a long interrogation time for probing the clock transition. Furthermore, it may be the foundation for developing our optical lattice clock of strontium atoms.
State-of-the-art optical clocks based on neutral atoms have already surpassed the world's best microwave atomic clocks in both accuracy and stability, paving the way to high-precision measurements of elementary aspects of nature, like the search for the drift of fundamental constants or the application of relativistic geodesy.These clocks operate with ensembles trapped in an optical lattice.Normally, high-power trapping laser fields induce a large AC Stark shift on the clock's transition frequency, as the clock states have different polarizabilities.A key feature of lattice clocks is the magic wavelength, for which the atomic polarizabilities of the clock states are equal, therefore compensating a differential frequency shift on the clock transition.In the periodic potential of the optical lattice, the energy spectrum of motional states features a band structure, analogous to electrons in a crystalline structure well-known from solid state physics.Within this band structure, atoms can tunnel between adjacent lattice sites.As a consequence from tunneling motion, the clock transition experiences a frequency shift and a broadening, which becomes pronounced in the shallow lattice regime.This work presents the first demonstration of a 24 Mg optical lattice clock including the precise determination of the frequency of the clock transition, its magic wavelength and its second-order Zeeman shift.Furthermore, the effect of tunneling in an optical lattice for magnesium has been extensively studied via optical spectroscopy of Bloch bands and substantiated with theoretical models, that were initially developed for a strontium optical lattice clock.Measuring lattice light induced frequency shifts of the clock transition for various lattice wavelengths and intensities, yielded a value of the magic wavelength of the 1 S 0 → 3 P 0 clock transition in 24 Mg of 468.463(207) nm.This value is in well agreement with a recent theoretical calculation of 468.45(23) nm, using a refined atomic structure model.The experimental value for the magic wavelength was independently verified with optical spectroscopy of Bloch bands carried out on the clock transition.Here, the AC Stark modified band structure is directly probed by a single frequency scan of the carrier resonance, featuring an asymmetric line shape, that is strongly dependent on the lattice wavelength.This technique demonstrates a novel method for the determination of the magic wavelength and could also be applied to other atomic species.In bosonic isotopes of alkaline earth(-like) elements, like 24 Mg, optical dipole excitation of the spin-forbidden 1 S 0 → 3 P 0 clock transition can be enhanced, e.g. by applying an external magnetic field.While these bosons are insensitive to first-order Zeeman shifts, the second-order Zeeman effect displays a dominant contribution to the clock's error budget.In this thesis, the magnetic polarizability β is measured to be -206.6(2.0)MHz/T 2 , consistent with a theoretical calculation, and the clock transition frequency was found to be 655 058 646 691(101) kHz.
We demonstrate a spin-polarized clock transition spectrum of the 87Sr optical lattice clock. The clock transition 5s2 1S05s5p 3P0 of isotope 87Sr has a hyperfine structure due to non-zero nuclear spin, inducing ten -polarized transitions from each individual mF state under the condition of a bias magnetic field along the probing polarization axis. In this experiment, atoms are driven to a certain mF state by a circular-polarization pump light to maximize the atomic population, which is beneficial to the stability and uncertainty evaluation of the optical lattice clock. After two stages cooling and trapping, about 3.5106 atoms are trapped in the red magneto-optical trap with a temperature of 3.9 K. A grating-feedback external cavity diode laser with a tapered amplifier is used to build the optical lattice with a magic-wavelength of 813.426 nm. Both waists of the counter-propagating lattice beam along the horizontal direction are overlapped to form a one-dimensional (1D) optical lattice. The lifetime of the atoms trapped in the 1D optical lattice is 1600 ms. The clock laser at 698 nm is a grating-feedback diode laser, which is locked to an ultra-low expansion cavity by the Pound-Drever-Hall technique to stabilize the frequency and phase. As a result, the linewidth of clock laser is narrowed to Hz level. By the normalized shelving method, we obtain a resolved sideband spectrum of 87Sr 5s2 1S05s5p 3P0 transition. According to the spectrum, the lattice temperature along the longitudinal direction is approximately 4.2 K. After that a linewidth of 6.7 Hz of the degenerate clock transition is obtained at a probing time of 150 ms by utilizing a three-dimensional (3D) bias magnetic field, which is used to eliminate the stray magnetic fields. Then a small bias magnetic field of 300 mGs is applied along the polarization axis of the lattice light to achieve the spectrum of Zeeman magnetic sublevels of the clock transition. Furthermore, the mF=+9/2 and mF=-9/2 magnetic sublevels are picked to be respectively pumped by the +-polarized and --polarized light at 689 nm, a variable liquid crystal wave plate is employed to switch on both polarizations. Finally, the spin polarized clock transition spectrum is obtained at the interrogating pulse of 150 ms, and the linewidths of the mF=+9/2, mF=-9/2 magnetic sublevel transitions are 6.8 Hz and 6.2 Hz respectively.
Accurate time keeping is critical to the function and advancement of many human endeavours. Atomic clocks based on a microwave transition in atomic Cs have served as primary frequency standards to realise the SI second since their formal adoption in 1967. State-of-the-art, laser cooled, Cs fountains now routinely operate with fractional frequency uncertainties below the 10⁻¹⁵ level in laboratories throughout the world. Over the last decade, efforts to build frequency standards based on optical transitions have come to fruition and potential inaccuracies below the 10⁻¹⁷ level have been demonstrated. Such standards point to the future of time keeping and much development is being pursued to realise the potential of these 'next generation' optical clocks. One such approach, on which this work focusses, relies on a 'magic' wavelength optical lattice trap to provide (almost) Doppler- and recoil-free confinement of atoms during clock interrogation. At this 'magic' wavelength, light induced perturbation of the clock states is equal and so cancels precisely. This thesis describes the design and implementation of an optical lattice frequency standard apparatus based on 88Sr held in a 1D optical lattice. A review of the development of atomic frequency metrology is given from a historical viewpoint and the technology and limitations of current methods discussed. To tackle the blackbody radiation shift, which currently presents the greatest limitation to the Sr lattice clock, imposing at the 10⁻¹⁶ level, a scheme to measure the blackbody radiation shift coefficient at the 10⁻¹⁷ level is developed. Techniques to laser cool and trap atomic strontium are described and the implementation detailed. All laser systems required for clock operation are described including the design and implementation of extended-cavity diode lasers for precision spectroscopy. Details relevant to the eventual operation of the apparatus are discussed.
We report on recent realization of an optical lattice clock operating on the1S0-3P0transition in88Sr, at LENS laboratories. The clock transition is excited with the technique of magnetic field-induced spectroscopy. New experimental techniques has also been developed in order to simplifies the clock spectroscopy in Sr atoms. The first new method helps in the first search of the clock transition without the use of extensive frequency metrology hardware and in particular optical frequency combs. This technique exploits a near coincidence in the atomic wavelengths of the1S0-3P0clock and1S0-3P1second stage cooling transitions in Sr, which are only 5 THz far apart. This coincidence enables the use of an optical (transfer) cavity to reference the frequency of the clock transition relative to that of the much stronger cooling transition. Secondly we reduce the complexity of the experimental setup by using only semiconductor laser sources in the apparatus. With this setup, about 10488Sr atoms are trapped in a 1D lattice formed by 200 mW of radiation tuned near the magic wavelength at 813 nm. We will present a first uncertainty budget for our optical lattice clock based on88Sr with particular attention to density dependent collisions, which led to an unexpectedly high signal contrast for long interaction times. In view of an absolute frequency measurement of clock transition we'll also present recent experimental results on optimization of an home made Ti:Sa optical frequency comb. Additionally, we anticipate that the simplification of the experimental setup presented will help address a wider range of applications including those requiring transportable devices. Along these lines we will report progress on the realization of the first transportable Sr optical lattice clock.
We report on our progress toward the realization of a compact optical frequency standard referenced to strontium intercombination lines. Our current setup allows the production of ultracold Sr atoms in hundreds of ms. For high resolution spectroscopy of the 1S0-3P0 doubly forbidden transition we have prepared a 698 nm clock laser stabilized on a high finesse, symmetrically suspended cavity and a high power 813 nm light source for the optical lattice trap at the magic wavelength. Due to their compactness, reliability, and low power consumption, semiconductor laser sources represent the best choice for the development of compact and transportable devices for application both on Earth and in Space. A new Sr trapping and cooling experimental setup is also presented.
We present experimental results for an optical lattice clock operating on the1S0harr3P0transition in88Sr, which is excited with the technique of magnetic field-induced spectroscopy To reduce the complexity of the setup we have developed a set of new experimental techniques that greatly simplifies the clock spectroscopy in Sr atoms. First, we developed a method for finding the clock transition that removes the need for extensive frequency metrology hardware and optical frequency combs. This technique exploits a near coincidence in the atomic wavelengths of the1S0harr3P0clock and1S0harr3P1second stage cooling transitions in Sr, which are only 5 THz far apart. This coincidence enables the use of an optical (transfer) cavity to reference the frequency of the clock transition relative to that of the much stronger coolign transition Second, all laser sources in the experimental setup are based on semiconductor technology, which greatly reduces the complexity of the apparatus. With this setup, about 10488Sr atoms are trapped in a 1D lattice formed by 200 mW of radiation tuned near the magic wavelength at 813 nm. Preliminar uncertainty budget for our optical lattice clock is also presented, with particular attention to density dependent collisions, which led to an unexpectedly high signal contrast for long interaction times.