The Stark shift due to blackbody radiation (BBR) is the key factor limiting the performance of many atomic frequency standards, with the BBR environment inside the clock apparatus being difficult to characterize at a high level of precision. Here we demonstrate an in-vacuum radiation shield that furnishes a uniform, well-characterized BBR environment for the atoms in an ytterbium optical lattice clock. Operated at room temperature, this shield enables specification of the BBR environment to a corresponding fractional clock uncertainty contribution of 5.5×10(-19). Combined with uncertainty in the atomic response, the total uncertainty of the BBR Stark shift is now 1×10(-18). Further operation of the shield at elevated temperatures enables a direct measure of the BBR shift temperature dependence and demonstrates consistency between our evaluated BBR environment and the expected atomic response.
The Stark shift due to blackbody radiation (BBR) is the key factor limiting the performance of many atomic frequency standards, with the BBR environment inside the clock apparatus being difficult to characterize at a high level of precision. Here we demonstrate an in-vacuum radiation shield that furnishes a uniform, well-characterized BBR environment for the atoms in an ytterbium optical lattice clock. Operated at room temperature, this shield enables specification of the BBR environment to a corresponding fractional clock uncertainty contribution of 5.5×10(-19). Combined with uncertainty in the atomic response, the total uncertainty of the BBR Stark shift is now 1×10(-18). Further operation of the shield at elevated temperatures enables a direct measure of the BBR shift temperature dependence and demonstrates consistency between our evaluated BBR environment and the expected atomic response.
Controlling the Stark perturbation from ambient thermal radiation is key to advancing the performance of many atomic frequency standards. This thermal radiation perturbs the atomic energy levels, inducing a Stark shift to the clock frequency conventionally known as the BBR shift. For over four decades, the BBR shift has been a persistent challenge in the pursuit of better atomic clock performance. For room-temperature optical lattice clocks (OLCs) based on Yb and Sr, the BBR shift represents the largest uncanceled systematic frequency shift while typically also constituting the largest source of uncertainty in these state-of-the-art clocks at the ≈ 1 × 10−18 level. In this thesis, I report on the design, assembly and integration of a BBR enclosure, or “shield,” that achieves an unprecedented BBR shift uncertainty of 1.7 × 10−20 by furnishing the interrogated atoms with a near-ideal BBR environment at a cryogenic temperature, while still allowing all the critical quantum control functions required for clock operation. Also, I present a novel lattice loading technique, known as ratchet loading, which enables programmable control over the spatial distribution of ultra-cold atoms confined in an optical lattice. This method allows for the loading of a large number of atoms, effectively reducing quantum projection noise (QPN) while also mitigating frequency shifts caused by atomic interactions. Additionally, ratchet loading facilitates the creation of spatially resolved atomic ensembles along the lattice, making it particularly useful for lattice light shift measurements and potentially advantageous for emerging techniques that probe atomic coherence beyond the local oscillator (LO) coherence time. With the near-elimination of blackbody radiation (BBR) uncertainty and improved clock stability for systematic evaluations, the realization of a mid- to low-10−19 uncertainty Yb optical lattice clock is now more attainable than ever.
Abstract Here we present a liquid nitrogen-cooled Ca+ optical clock with an overall systematic uncertainty of 3×10-18. In contrast with the room-temperature Ca+ optical clock that we have reported previously, the temperature of the blackbody radiation (BBR) shield in vacuum has been reduced to 82(5) K using liquid nitrogen. An ion trap with a lower heating rate and improved cooling lasers were also introduced. This allows cooling the ion temperature to the Doppler cooling limit during the clock operation, and the systematic uncertainty due to the ion’s secular (thermal) motion is reduced to < 1×10-18. The uncertainty due to the probe laser light shift and the servo error are also reduced to < 1×10-19 and 4×10-19 with the hyper-Ramsey method and the higher-order servo algorithm, respectively. By comparing the output frequency of the cryogenic clock to that of a room-temperature clock, the differential BBR shift between the two was measured with a fractional statistical uncertainty of 7×10-18. The differential BBR shift was used to calculate the static differential polarizability, and it was found in excellent agreement with our previous measurement with a different method. This work suggests that the BBR shift of optical clocks can be well suppressed in a liquid nitrogen environment. This is advantageous because conventional liquid-helium cryogenic systems for optical clocks are more expensive and complicated. Moreover, the proposed system can be used to suppress the BBR shift significantly in other types of optical clocks such as Yb+, Sr+, Yb, Sr, etc.
Abstract We develop a method of synthetic frequency generation to construct an atomic clock with blackbody radiation (BBR) shift uncertainties below 10−19 at environmental conditions with a very low level of temperature control. The proposed method can be implemented for atoms and ions, which have two different clock transitions with frequencies ν 1 and ν 2 allowing to form a synthetic reference frequency ν syn = (ν 1 − ɛν 2)/(1 − ɛ), which is absent in the spectrum of the involved atoms or ions. Calibration coefficient ɛ can be chosen such that the temperature dependence of the BBR shift for the synthetic frequency ν syn has a local extremum at an arbitrary operating temperature T 0. This leads to a weak sensitivity of BBR shift with respect to the temperature variations near operating temperature T 0. As a specific example, the Yb+ ion is studied in detail, where the utilized optical clock transitions are of electric quadrupole (S → D) and octupole (S → F) type. In this case, temperature variations of ±7 K lead to BBR shift uncertainties of less than 10−19, showing the possibility to construct ultra-precise combined atomic clocks (including portable ones) without the use of cryogenic techniques.
Presently, the Stark effect contributes the largest source of uncertainty in a ytterbium optical atomic clock through blackbody radiation. By employing an ultracold, trapped atomic ensemble and high stability optical clock, we characterize the quadratic Stark effect with unprecedented precision. We report the ytterbium optical clock's sensitivity to electric fields (such as blackbody radiation) as the differential static polarizability of the ground and excited clock levels ${\ensuremath{\alpha}}_{\mathrm{clock}}=36.2612(7)\text{ }\text{ }\mathrm{kHz}\text{ }(\mathrm{kV}/\mathrm{cm}{)}^{\ensuremath{-}2}$. The clock's uncertainty due to room temperature blackbody radiation is reduced by an order of magnitude to $3\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}17}$.
A major obstacle for optical clocks is the frequency shift due to black body radiation. We discuss how one can tackle this problem in an optical lattice clock; in our case 87-Sr: firstly, by a measurement of the dc Stark shift of the clock transition and, secondly, by interrogating the atoms in a cryogenic environment. Both approaches rely on transporting ultracold atoms over several cm within a probe cycle. We evaluate this approach of mechanically moving the optical lattice and conclude that it is feasible to transport the atoms over 50 mm within 300 ms. With this transport a dc Stark shift measurement will allow to reduce the contribution of the blackbody radiation to the fractional uncertainty below 2 * 10^-17 at room temperature by improving the shift coefficient known only from atomic structure calculations up to now. We propose a cryogenic environment at 77 K that will reduce this contribution to few parts in 10^-18.
Frequency standards based on optical transitions between electronic states of trapped ions have reached uncertainties below 10−18 [1]. The Stark shift caused by room-temperature blackbody radiation (BBR) causes the largest correction for most high-performance optical clock. The systematic uncertainty of 171Yb+ clocks based on the 2S1/2 (F = 0) → 2D3/2 (F = 2) electric quadrupole (E2) and 2S1/2 (F = 0) → 2F7/2 (F = 3) electric octupole (E3) transitions is currently limited to 28×10−18 and 1.5×10−18, respectively, by the fractional accuracy of the differential polarizability Δαdc of approximately 2% [2]. In the scope of this thesis, a dual species clock based on 171Yb+ and 88Sr+ ions was set up, operated and evaluated, to overcome this barrier. Since Δαdc is known with a smaller fractional uncertainty of 0.04% for the 2S1/2 → 2D5/2 E2 transition of 88Sr+ [3], this allows for a transfer of Δαdc from 88Sr+ to 171Yb+ following a method proposed in [4]. The optical intensity of a laser is calibrated with the Stark shift it causes on the 88Sr+ clock transition, allowing for the determination of Δαdc of the 171Yb+ clock transitions. This allows for a reduction of the fractional uncertainty of Δαdc for both 171Yb+ clock transitions below 0.4% and clock operation on the E2 and E3 transition with a fractional BBR shift uncertainty of 0.84×10−18 and 0.24×10−18 is enabled, respectively. However the value of Δαdc determined in this thesis does not agree with [2], a fractional offset of approximately 14% is observed. To investigate this discrepancy further, Δαdc is measured in the same manner as in [2] for the 88Sr+ clock transition. The same offset of approximately 14% is found, calling the accuracy of at least one of these methods into question. Finally, the first optical frequency ratio ℛ between the 88Sr+ clock transition and the 171Yb+ E3 transition is measured. The fractional uncertainty of ℛ is 23×10−18. ℛ in combination with the absolute frequency of the E3 transition allows for the determination of the 88Sr+ absolute frequency νSr+ with an uncertainty limited by the caesium references. The value of νSr+ falls outside of the recommended range, but is corroborated by measurements of the same quantity by other institutes [5, 6]. [1] M. Marshall et al., Phys. Rev. Lett. 135, 033201 (2025) [2] N. Huntemann et al., Phys. Rev. Lett. 116, 063001 (2016) [3] T. Lindvall et al., Phys. Rev. Lett. 135, 043402 (2025) [4] M. D. Barrett et al., Phys. Rev. A 100, 043418 (2019) [5] C. Marceau et al., Metrologia 62.4, 045001 (2025) [6] T. Lindvall et al., Phys. Rev. Appl. 24, 044082 (2025)