We report the realization of quantum logic spectroscopy on the 1 S 0→ 3 P 0 clock transition of a single 27 Al + ion. This ion is trapped together with a 40 Ca + ion in a linear Paul trap, coupled by Coulomb repulsion, which provides sympathetic Doppler laser cooling and also the means for internal state detection of the clock state of the 27 Al + ion. A repetitive quantum nondemolition measurement is performed to improve the fidelity of state detection. These techniques are applied to obtain clock spectroscopy at approximately 45 Hz. We also perform the preliminary locking on the 1 S 0 → 3 P 0 clock transition. Our work is a fundamental step that is necessary toward obtaining an ultra-precision quantum logic clock based on 40 Ca +-27 Al + ions.
We report the realization of quantum logic spectroscopy on the 1 S 0→ 3 P 0 clock transition of a single 27 Al + ion. This ion is trapped together with a 40 Ca + ion in a linear Paul trap, coupled by Coulomb repulsion, which provides sympathetic Doppler laser cooling and also the means for internal state detection of the clock state of the 27 Al + ion. A repetitive quantum nondemolition measurement is performed to improve the fidelity of state detection. These techniques are applied to obtain clock spectroscopy at approximately 45 Hz. We also perform the preliminary locking on the 1 S 0 → 3 P 0 clock transition. Our work is a fundamental step that is necessary toward obtaining an ultra-precision quantum logic clock based on 40 Ca +-27 Al + ions.
We perform quantum logic spectroscopy with a 27 Al + / 40 Ca + mixed ion crystal in a linear Paul trap for a measurement of the intercombination transition in 27 Al + . Towards this end, Ramsey spectroscopy is used for probing the transition in 27 Al + and the clock transition in 40 Ca + in interleaved measurements. By using the precisely measured frequency of the clock transition in 40 Ca + as a frequency reference, we determine the frequency of the intercombination line to be = 1 122 842 857 334 736 (85) Hz and the Landé g -factor of the excited state to be = 0.428 133(2).
We report, for the first time, laser spectroscopy of the 1S0-->3P0 clock transition in 27Al+. A single aluminum ion and a single beryllium ion are simultaneously confined in a linear Paul trap, coupled by their mutual Coulomb repulsion. This coupling allows the beryllium ion to sympathetically cool the aluminum ion and also enables transfer of the aluminum's electronic state to the beryllium's hyperfine state, which can be measured with high fidelity. These techniques are applied to measure the clock transition frequency nu=1,121,015,393,207,851(6) Hz. They are also used to measure the lifetime of the metastable clock state tau=20.6+/-1.4 s, the ground state 1S0 g factor gS=-0.000,792,48(14), and the excited state 3P0 g factor gP=-0.001,976,86(21), in units of the Bohr magneton.
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.
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.
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.
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.