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arXiv:0803.1039 · Physical Review Letters

Frequency Shifts in an Optical Lattice Clock Due to Magnetic-Dipole and Electric-Quadrupole Transitions

А. В. Тайченачев, Valeriy I. Yudin, Vitalii D Ovsiannikov, Vitalii G Pal'chikov, Chris W. Oates

Published Nov 4, 2008• 56 citations
arXivHTMLPDF

Abstract

We report a hitherto undiscovered frequency shift for forbidden J = 0-->J = 0 clock transitions excited in atoms confined to an optical lattice. These shifts result from magnetic-dipole and electric-quadrupole transitions, which have a spatial dependence in an optical lattice that differs from that of the stronger electric-dipole transitions. In combination with the residual translational motion of atoms in an optical lattice, this spatial mismatch leads to a frequency shift via differential energy level spacing in the lattice wells for ground state and excited state atoms. We estimate that this effect could lead to fractional frequency shifts as large as 10(-16), which might prevent lattice-based optical clocks from reaching their predicted performance levels. Moreover, these effects could shift the magic wavelength in lattice clocks in three dimensions by as much as 100 MHz, depending on the lattice configuration.

DOI
10.1103/physrevlett.101.193601

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We report a hitherto undiscovered frequency shift for forbidden J = 0-->J = 0 clock transitions excited in atoms confined to an optical lattice. These shifts result from magnetic-dipole and electric-quadrupole transitions, which have a spatial dependence in an optical lattice that differs from that of the stronger electric-dipole transitions. In combination with the residual translational motion of atoms in an optical lattice, this spatial mismatch leads to a frequency shift via differential energy level spacing in the lattice wells for ground state and excited state atoms. We estimate that this effect could lead to fractional frequency shifts as large as 10(-16), which might prevent lattice-based optical clocks from reaching their predicted performance levels. Moreover, these effects could shift the magic wavelength in lattice clocks in three dimensions by as much as 100 MHz, depending on the lattice configuration.
In a standing wave of light, a difference in spatial distributions of multipolar atom-field interactions may introduce atomic-motion dependent clock uncertainties in optical lattice clocks. We show that the magic wavelength can be defined so as to eliminate the spatial mismatch in electric dipole, magnetic dipole, and electric quadrupole interactions for specific combinations of standing waves by allowing a spatially constant light shift arising from the latter two interactions. Experimental prospects of such lattices used with a blue magic wavelength are discussed.
We consider the frequency shift in optical lattice clocks which arises from the coupling of the electronic motion to the atomic motion within the lattice. For the simplest of three-dimensional lattice geometries this coupling is shown to affect only clocks based on blue-detuned lattices. We have estimated the size of this shift for the prospective strontium lattice clock operating at the 390-nm blue-detuned magic wavelength. The resulting fractional frequency shift is found to be on the order of ${10}^{\ensuremath{-}18}$ and is largely overshadowed by the electric quadrupole shift. For lattice clocks based on more complex geometries or other atomic systems, this shift could potentially be a limiting factor in clock accuracy.
In a standing wave of light, a difference in spatial distributions of multipolar atom-field interactions may alter the definition of the magic wavelength to minimize the uncertainty of optical lattice clocks. We show that the magic wavelength can be determined so as to eliminate the spatial mismatch in electric dipole, magnetic dipole, and electric quadrupole interactions for specific combinations of standing waves. Experimental prospects of such lattices used with a blue magic wavelength are discussed.
We develop a method of spectroscopy that uses a weak static magnetic field to enable direct optical excitation of forbidden electric-dipole transitions that are otherwise prohibitively weak. The power of this scheme is demonstrated using the important application of optical atomic clocks based on neutral atoms confined to an optical lattice. The simple experimental implementation of this method--a single clock laser combined with a dc magnetic field--relaxes stringent requirements in current lattice-based clocks (e.g., magnetic field shielding and light polarization), and could therefore expedite the realization of the extraordinary performance level predicted for these clocks. We estimate that a clock using alkaline-earth-like atoms such as Yb could achieve a fractional frequency uncertainty of well below 10(-17) for the metrologically preferred even isotopes.
Abstract The energy levels and electric dipole ( E 1 ) matrix elements of the ground state and low-lying excited states of Be atoms are calculated using the relativistic configuration interaction plus core polarization (RCICP) method. The static and dynamic E 1 , magnetic dipole ( M 1 ) and electric quadrupole ( E 2 ) polarizabilities as well as the hyperpolarizabilities of the 2 s 2 1 S 0 and 2 s 2 p 3 P 0 states are determined. Two magic wavelengths, 300.03 and 252.28 nm, of 2 s 2 1 S 0 → 2 s 2 p 3 P 0 clock transition are found. Then, the multipolar and nonlinear Stark shifts of the clock transition at the magic wavelength are discussed in detail. We find that when the laser intensity I is in the range of 14.3–15.9 kW cm−2 and the detuning δ (the frequency detuning of the lattice laser frequency relative to the magic frequency) is in the range of 40.7–40.9 MHz, the fractional Stark shifts of the clock transition are less than 1.0 × 10−18. While, when I is in the range of 15.01–15.46 kW cm−2 and δ is in the range of 40.73–40.76 MHz, the fractional Stark shifts are lower than 1.0 × 10−19.
Optical lattice clocks combine the accuracy and stability required for next-generation frequency standards. At the heart of these clocks are carefully engineered optical lattices tuned to a wavelength where the differential AC Stark shift between ground and excited states vanishes—the so called ‘magic’ wavelength. To date, only alkaline-earth-like atoms utilizing clock transitions with total electronic angular momentum J=0 have successfully realized these magic wavelength optical lattices at the level necessary for state-of-the-art clock operation. In this article, we discuss two additional types of clock transitions utilizing states with J≠0, leveraging hyperfine structure to satisfy the necessary requirements for controlling lattice-induced light shifts. We propose realizing (i) clock transitions between same-parity clock states with total angular momentum F=0 and (ii) M1/E2 clock transitions between a state with F=0 and a second state with J=1/2, mF=0. We present atomic species which fulfill these requirements before giving a detailed discussion of both manganese and copper, demonstrating how these transitions provide the necessary suppression of fine structure-induced vector and tensor lattice light shifts for clock operations. Such realization of alternative optical lattice clocks promises to provide a rich variety of new atomic species for neutral atom clock operation, with applications from many-body physics to searches for new physics.