Magnesium ion which acts as the logic ion in27Al+ion optical clock is trapped and laser cooled in a linear ion trap. Rabi oscillation between two hyperfine ground states of25Mg+ion is observed and resonant frequency between two hyperfine ground states of25Mg+ion is measured. Earth magnetic field is compensated with three pairs of mutually perpendicular Helmholtz coils. Light shift induced by the Raman cooling beams is measured. With the photo-ionization laser of Al, Al+ion is trapped together with Mg+ion. The linewidth of the clock laser of the27Al+ion is measured to be about 0.8 Hz. The Allan deviation of the beat note from two independent lasers is 6.5×10-15at 1s.
Magnesium ion which acts as the logic ion in27Al+ion optical clock is trapped and laser cooled in a linear ion trap. Rabi oscillation between two hyperfine ground states of25Mg+ion is observed and resonant frequency between two hyperfine ground states of25Mg+ion is measured. Earth magnetic field is compensated with three pairs of mutually perpendicular Helmholtz coils. Light shift induced by the Raman cooling beams is measured. With the photo-ionization laser of Al, Al+ion is trapped together with Mg+ion. The linewidth of the clock laser of the27Al+ion is measured to be about 0.8 Hz. The Allan deviation of the beat note from two independent lasers is 6.5×10-15at 1s.
An aluminium ion optical clock is under development at Huazhong University of Science and Technology. The 25 Mg + ion is chosen as logic ion to sympathetically cool an Al + ion and to detect its states. The 25 Mg + ion is cooled to the motional ground state through Raman sideband cooling as the first step for quantum logic spectroscopy. Ultra-stable lasers for the interrogation of the clock transition are developed. The instability of the laser beat frequency is 1.2 x 10 -15 at 1 s, which is close to the thermal noise limit of the reference cavity.
The 435 mum171Yb+transition is a good candidate for an atomic clock based on an optical transition. We have stored single171Yb ions for several months in RF traps. The ions are cooled, repumped and the clock transition is interrogated by (frequency-doubled) diode lasers. The interrogation laser linewidth was 30 Hz determining the resolvable linewidth of the Yb+transition interrogated. The absolute frequency of this transition was measured using an optical comb generator, self referenced by broadening the spectrum to above one octave, with respect to a Cs fountain clock. Of all systematic frequency shifts to which this transition is subject an estimate indicates that the electric quadruple shift appears is the largest. To obtain a magnitude of the quadruple shift (and the quadruple moment) the clock frequencies of two independently stored and cooled171Yb ions were compared while varying the static electric field in one trap. The measured frequency shift amounting to ~1 Hz/V. This result would seem to permit clocks with much higher accuracy than the clocks based on microwave transition, particularly if the technique of aligning the ions with respect to the electric field were applicable. Anticipating even more precise clocks, we are presently investigating a blue nuclear transition in229Th. Such a nuclear transition should be even better shielded from environmental influences than transitions in the electron shell. This nuclear transition has not yet been directly optically observed. We are presently investigating the luminescence after incoherent broad band optical excitation. The triply ionized223Th is then a suitable system for trapped single ion spectroscopy. The cooling transition lies conveniently in the near infrared and the nuclear clock transition can be read out by nuclear/electron shell double resonance
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.
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.
We present a single solid-state laser system to cool, coherently manipulate and detect 25Mg+ ions. Coherent manipulation is accomplished by coupling two hyperfine ground state levels using a pair of far-detuned Raman laser beams. Resonant light for Doppler cooling and detection is derived from the same laser source by means of an electro-optic modulator, generating a sideband which is resonant with the atomic transition. We demonstrate ground-state cooling of one of the vibrational modes of the ion in the trap using resolved-sideband cooling. The cooling performance is studied and discussed by observing the temporal evolution of Raman-stimulated sideband transitions. The setup is a major simplification over existing state-of-the-art systems, typically involving up to three separate laser sources.