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.
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.
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 the cancellation of the differential ac Stark shift of the microwave hyperfine clock transition in trapped 87Rb atoms. Recent progress in metrology exploits so-called magic wavelengths, whereby an atomic ensemble can be trapped with laser light whose wavelength is chosen so that both levels of an optical atomic transition experience identical ac Stark shifts. Similar magic-wavelength techniques are not possible for the microwave hyperfine transitions in the alkali metals due to their simple electronic structure. We show, however, that ac Stark shift cancellation is indeed achievable for certain values of wavelength, polarization, and magnetic field. The cancellation comes at the expense of a small magnetic-field sensitivity. The technique demonstrated here has implications for experiments involving the precise control of optically trapped neutral atoms.
We propose a new class of atomic microwave clocks based on the hyperfine transitions in the ground state of aluminum or gallium atoms trapped in optical lattices. For such elements magic wavelengths exist at which both levels of the hyperfine doublet are shifted at the same rate by the lattice laser field, cancelling its effect on the clock transition. A similar mechanism for the magic wavelengths may work in microwave hyperfine transitions in other atoms which have the fine-structure multiplets in the ground state.
We demonstrate the cancellation of the differential ac Stark shift of the microwave hyperfine clock transition in trapped 87 Rb atoms. Recent progress in metrology exploits so-called “magic wavelengths,” whereby an atomic ensemble can be trapped with laser light whose wavelength is chosen so that both levels of an optical atomic transition experience identical ac Stark shifts. Similar magic-wavelength techniques are not possible for the microwave hyperfine transitions in the alkalis, due to their simple electronic structure. We show, however, that ac Stark shift cancellation is indeed achievable for certain values of wavelength, polarization, and magnetic field. The cancellation comes at the expense of a small magnetic-field sensitivity. The technique demonstrated here has implications for experiments involving the precise control of optically-trapped neutral atoms.
The circular polarized laser beam of the “magic” wavelength used to produce an optical lattice for the time-frequency standard on neutral atoms may mix the 3P 1 state to the long-living metastable state 3P 0 thus providing significant enhancement of the strongly forbidden 1S 0 -3P 0 clock transition in even isotopes of alkaline-earth-like atoms. We present a detailed analysis of various factors influencing resolution and uncertainty for this kind of optical standard, including precise estimations of the “magic” wavelengths, transition matrix elements and field induced second- and fourth-order ac Stark shifts for the ground and metastable alkaline-earth-like atoms.
The primary frequency and time standard, defined via a transition frequency of caesium-133, is realized by microwave clocks reaching relative uncertainties in the 10−^16 level. This performance has been surpassed by state-of-the-art lattice clocks, with transition frequencies in the optical regime, leading to two orders of magnitude lower uncertainties. The key to this performance is the confinement in the Lamb-Dicke regime at the magic wavelength enabling a Doppler- and recoil-free spectroscopy with a first-order suppressed AC Stark shift. In atomic clocks, several effects contribute to the uncertainty of the transition frequency. Through continuous global characterization efforts, the individual uncertainty of these effects have been subsequently reduced. Yet one effect, namely the frequency shift induced by blackbody radiation has been identified as a dominant contribution which is difficult to overcome by technical means. In this regard, magnesium-24 excels as a species of choice as its blackbody radiation sensitivity is one order of magnitude lower than in the most frequently used atomic clock species. Furthermore, magnesium offers a relatively simple electronic structure which enables theoretical support through high-precision calculations. This thesis features the first characterization of a magnesium optical lattice clock operating at the magic wavelength. The characterization of the magnesium frequency standard presented in this thesis depends essentially on the resolution of the transition linewidth, which could be reduced from kHz range to 51(3) Hz in a complementing work. The realization of a transition linewidth with a quality factor of Q = 1.3 × 10^13 has contributed to an improved determination of the magic wavelength within this thesis to 468.4106(2) nm. Compared to earlier work, this represents an improvement of two orders of magnitude. Furthermore, the lower transition linewidth also allowed the first observation of the probe AC Stark shift and thus the first characterization of effects in the lattice that falsify the frequency of the trapped magnesium atoms. Overall, the relative uncertainty of the frequency-related effects influencing the clock transition could be determined to be 7.1 × 10^−15. The dominant contributions can be assigned to tunneling broadening and the lattice and probe AC Stark effects, induced by the probe and lattice light. All these effects can be traced back to technical limitations and are part of future work. Following the characterization, a first frequency comparison between the magnesium lattice clock against the primary frequency standard as well as the ytterbium ion clock at the PTB has been performed and thus a first realization of a lattice based frequency standard with magnesium atoms was demonstrated. The determined transition frequency of 655 058 646 681 864.1(5.3) Hz complies with former measurements. The primary frequency and time standard, defined via a transition frequency of caesium-133, is realized by microwave clocks reaching relative uncertainties in the 10^−16 level. This performance has been surpassed by state-of-the-art lattice clocks, with transition frequencies in the optical regime, leading to two orders of magnitude lower uncertainties. The key to this performance is the confinement in the Lamb-Dicke regime at the magic wavelength enabling a Doppler- and recoil-free spectroscopy with a first-order suppressed AC Stark shift. In atomic clocks, several effects contribute to the uncertainty of the transition frequency. Through continuous global characterization efforts, the individual uncertainty of these effects have been subsequently reduced. Yet one effect, namely the frequency shift induced by blackbody radiation has been identified as a dominant contribution which is difficult to overcome by technical means. In this regard, magnesium-24 excels as a species of choice as its blackbody radiation sensitivity is one order of magnitude lower than in the most frequently used atomic clock species. Furthermore, magnesium offers a relatively simple electronic structure which enables theoretical support through high-precision calculations. This thesis features the first characterization of a magnesium optical lattice clock operating at the magic wavelength. The characterization of the magnesium frequency standard presented in this thesis depends essentially on the resolution of the transition linewidth, which could be reduced from kHz range to 51(3) Hz in a complementing work. The realization of a transition linewidth with a quality factor of Q = 1.3 × 10^13 has contributed to an improved determination of the magic wavelength within this thesis to 468.4106(2) nm. Compared to earlier work, this represents an improvement of two orders of magnitude. Furthermore, the lower transition linewidth also allowed the first observation of the probe AC Stark shift and thus the first characterization of effects in the lattice that falsify the frequency of the trapped magnesium atoms. Overall, the relative uncertainty of the frequency-related effects influencing the clock transition could be determined to be 7.1 × 10^−15. The dominant contributions can be assigned to tunneling broadening and the lattice and probe AC Stark effects, induced by the probe and lattice light. All these effects can be traced back to technical limitations and are part of future work. Following the characterization, a first frequency comparison between the magnesium lattice clock against the primary frequency standard as well as the ytterbium ion clock at the PTB has been performed and thus a first realization of a lattice based frequency standard with magnesium atoms was demonstrated. The determined transition frequency of 655 058 646 681 864.1(5.3) Hz complies with former measurements.