This paper presents an overview of the Al+ optical clock, which is based on quantum logic spectroscopy and provides the most accurate frequency measurement ever reported. Dehmelt’s original design of the optical clock was not realized due to the difficulty in generating the vacuum ultraviolet radiation necessary for laser cooling and the ion’s quantum state detection. The problem was solved by sympathetically cooling the ion with another ion and detecting the quantum state using the ancillary ion. The method, which is called quantum logic spectroscopy, comes from the use of phonon qubit as a bus of the quantum state of the ions in the Cirac-Zoller ion-trap quantum computer. The clock can be simplifi ed by introducing direct excitation by vacuum ultraviolet radiation or another ion species. The clock’s stability will be improved more than ten times by a middle-term stabilized clock laser.
This paper presents an overview of the Al+ optical clock, which is based on quantum logic spectroscopy and provides the most accurate frequency measurement ever reported. Dehmelt’s original design of the optical clock was not realized due to the difficulty in generating the vacuum ultraviolet radiation necessary for laser cooling and the ion’s quantum state detection. The problem was solved by sympathetically cooling the ion with another ion and detecting the quantum state using the ancillary ion. The method, which is called quantum logic spectroscopy, comes from the use of phonon qubit as a bus of the quantum state of the ions in the Cirac-Zoller ion-trap quantum computer. The clock can be simplifi ed by introducing direct excitation by vacuum ultraviolet radiation or another ion species. The clock’s stability will be improved more than ten times by a middle-term stabilized clock laser.
Direct Laser Cooling Al+ Ion Optical Clocks
The Al ion optical clock is a very promising optical frequency standard candidate due to its extremely small black-body radiation shift. It has been successfully demonstrated with the indirect cooled, quantum-logic-based spectroscopy technique. Its accuracy is limited by second-order Doppler shift, and its stability is limited by the number of ions that can be probed in quantum logic processing. We propose a direct laser cooling scheme of Al ion optical clocks where both the stability and accuracy of the clocks are greatly improved. In the proposed scheme, two Al traps are utilized. The first trap is used to trap a large number of Al ions to improve the stability of the clock laser, while the second trap is used to trap a single Al ion to provide the ultimate accuracy. Both traps are cooled with a continuous wave 167 nm laser. The expected clock laser stability can reach . For the second trap, in addition to 167 nm laser Doppler cooling, a second stage pulsed 234 nm two-photon cooling laser is utilized to further improve the accuracy of the clock laser. The total systematic uncertainty can be reduced to about . The proposed Al ion optical clock has the potential to become the most accurate and stable optical clock .
We report a single-ion optical atomic clock with a fractional frequency uncertainty of 5.5×10^{-19} and fractional frequency stability of 3.5×10^{-16}/sqrt[τ/s], based on quantum logic spectroscopy of a single ^{27}Al^{+} ion. A cotrapped ^{25}Mg^{+} ion provides sympathetic cooling and quantum logic readout of the ^{27}Al^{+}^{1}S_{0}↔^{3}P_{0} clock transition. A Rabi probe duration of 1 s, enabled by laser stability transfer from a remote cryogenic silicon cavity across a 3.6 km fiber link, results in a threefold reduction in instability compared to previous ^{27}Al^{+} clocks. Systematic uncertainties are lower due to an improved ion trap electrical design, which reduces excess micromotion, and a new vacuum system, which reduces collisional shifts. We also perform a direction-sensitive measurement of the ac magnetic field due to the rf ion trap, eliminating systematic uncertainty due to field orientation.
We have constructed an optical clock with a fractional frequency inaccuracy of 8.6x10{-18}, based on quantum logic spectroscopy of an Al+ ion. A simultaneously trapped Mg+ ion serves to sympathetically laser cool the Al+ ion and detect its quantum state. The frequency of the {1}S{0}<-->{3}P{0} clock transition is compared to that of a previously constructed Al+ optical clock with a statistical measurement uncertainty of 7.0x10{-18}. The two clocks exhibit a relative stability of 2.8x10{-15}tau{-1/2}, and a fractional frequency difference of -1.8x10{-17}, consistent with the accuracy limit of the older clock.
Scaling trapped-ion quantum sensors from single ions to large ensembles is a key challenge for next-generation precision measurements. At the same time, many ion species of interest for optical clocks and tests of fundamental physics lack closed cycling transitions required for direct laser cooling and state detection. Collective quantum logic spectroscopy addresses both limitations by coupling an ensemble of sensor, or spectroscopy, ions to one or more logic ions that provide sympathetic cooling and state readout. Here, we establish the fundamental performance limits and operating regimes of this protocol, identifying how the interaction strength, interrogation time, and logic-ensemble size govern sensitivity, dynamic range, and robustness to experimental imperfections. We show that quantum-limited sensitivity can be retained even with a single logic ion, while increasing the number of logic ions substantially improves readout efficiency and robustness. Beyond precision metrology, the same collective interface enables many-body measurements relevant to quantum information processing, including parity measurements and stabilizer-like syndrome extraction. Our results establish collective quantum logic spectroscopy as a scalable framework for optical clocks, quantum-enhanced sensing, and trapped-ion quantum information processing.
We present a general technique for precision spectroscopy of atoms that lack suitable transitions for efficient laser cooling, internal state preparation, and detection. In our implementation with trapped atomic ions, an auxiliary "logic" ion provides sympathetic laser cooling, state initialization, and detection for a simultaneously trapped "spectroscopy" ion. Detection is achieved by applying a mapping operation to each ion, which results in a coherent transfer of the spectroscopy ion's internal state onto the logic ion, where it is then measured with high efficiency. Experimental realization, by using 9Be+ as the logic ion and 27Al+ as the spectroscopy ion, indicates the feasibility of applying this technique to make accurate optical clocks based on single ions.
With the advent of optical clocks featuring fractional frequency uncertainties on the order of 10-17 and below, new applications such as chronometric leveling with few-centimeter height resolution emerge. We are developing a transportable optical clock based on a single trapped aluminum ion, which is interrogated via quantum logic spectroscopy. We employ singly charged calcium as the logic ion for sympathetic cooling, state preparation, and readout. Here, we present a simple and compact physics and laser package for manipulation of 40Ca+. Important features are a segmented multilayer trap with separate loading and probing zones, a compact titanium vacuum chamber, a near-diffraction-limited imaging system with high numerical aperture based on a single biaspheric lens, and an all-in-fiber 40Ca+ repump laser system. We present preliminary estimates of the trap-induced frequency shifts on 27Al+, derived from measurements with a single calcium ion. The micromotion-induced second-order Doppler shift for 27Al+ has been determined to be δνEMMν=-0.4-0.3 +0.4×10-18 and the black-body radiation shift is δνBBR/ν = (-4.0 ± 0.4) × 10-18. Moreover, heating rates of 30 (7) quanta per second at trap frequencies of ωrad,Ca+ ≈ 2π × 2.5 MHz (ωax,Ca+ ≈ 2π × 1.5 MHz) in radial (axial) direction have been measured, enabling interrogation times of a few hundreds of milliseconds.