Ian D. Leroux

We present a novel method for engineering an optical clock transition that is robust against external field fluctuations and is able to overcome limits resulting from field inhomogeneities. The technique is based on the application of continuous driving fields to form a pair of dressed states essentially free of all relevant shifts. Specifically, the clock transition is robust to magnetic shifts, quadrupole and other tensor shifts, and amplitude fluctuations of the driving fields. The scheme is applicable to either a single ion or an ensemble of ions, and is relevant for several types of ions, such as $^{40}\mathrm{Ca}^{+}$, $^{88}\mathrm{Sr}^{+}$, $^{138}\mathrm{Ba}^{+}$ and $^{176}\mathrm{Lu}^{+}$. Taking a spherically symmetric Coulomb crystal formed by 400 $^{40}\mathrm{Ca}^{+}$ ions as an example, we show through numerical simulations that the inhomogeneous linewidth of tens of Hertz in such a crystal together with linear Zeeman shifts of order 10~MHz are reduced to form a linewidth of around 1~Hz. We estimate a two-order-of-magnitude reduction in averaging time compared to state-of-the art single ion frequency references, assuming a probe laser fractional instability of $10^{-15}$. Furthermore, a statistical uncertainty reaching $2.9\times 10^{-16}$ in 1~s is estimated for a cascaded clock scheme in which the dynamically decoupled Coulomb crystal clock stabilizes the interrogation laser for an $^{27}\mathrm{Al}^{+}$ clock.

We introduce and demonstrate double-bright electromagnetically induced transparency (D-EIT) cooling as a novel approach to EIT cooling. By involving an additional ground state, two bright states can be shifted individually into resonance for cooling of motional modes of frequencies that may be separated by more than the width of a single EIT cooling resonance. This allows three-dimensional ground state cooling of a $^{40}$Ca$^+$ ion trapped in a linear Paul trap with a single cooling pulse. Measured cooling rates and steady-state mean motional quantum numbers for this D-EIT cooling are compared with those of standard EIT cooling as well as concatenated standard EIT cooling pulses for multi-mode cooling. Experimental results are compared to full density matrix calculations. We observe a failure of the theoretical description within the Lamb-Dicke regime that can be overcome by a time-dependent rate theory. Limitations of the different cooling techniques and possible extensions to multi-ion crystals are discussed.

In many of the high-precision optical frequency standards with trapped atoms or ions that are under development to date, the AC Stark shift induced by thermal radiation leads to a major contribution to the systematic uncertainty. We present an analysis of the inhomogeneous thermal environment experienced by ions in various types of ion traps. Finite element models which allow the determination of the temperature of the trap structure and the temperature of the radiation were developed for 5 ion trap designs, including operational traps at PTB and NPL and further optimized designs. Models were refined based on comparison with infrared camera measurement until an agreement of better than 10% of the measured temperature rise at critical test points was reached. The effective temperature rises of the radiation seen by the ion range from 0.8 K to 2.1 K at standard working conditions. The corresponding fractional frequency shift uncertainties resulting from the uncertainty in temperature are in the 10-18 range for optical clocks based on the Sr+ and Yb+ E2 transitions, and even lower for Yb+ E3, In+ and Al+. Issues critical for heating of the trap structure and its predictability were identified and design recommendations developed.

We demonstrate phase locking of a 729 nm diode laser to a 1542 nm master laser via an erbium-doped-fiber frequency comb, using a transfer-oscillator feedforward scheme which suppresses the effect of comb noise in an unprecedented 1.8 MHz bandwidth. We illustrate its performance by carrying out coherent manipulations of a trapped calcium ion with 99 % fidelity even at few-microsecond timescales. We thus demonstrate that transfer-oscillator locking can provide sufficient phase stability for high-fidelity quantum logic manipulation even without pre-stabilization of the slave diode laser.

Optical clocks based on ensembles of trapped ions offer the perspective of record frequency uncertainty with good short-term stability. Most suitable atomic species lack closed transitions for fast detection such that the clock signal has to be read out indirectly through transferring the quantum state of clock ions to co-trapped logic ions by means of quantum logic operations. For ensembles of clock ions existing methods for quantum logic readout require a linear overhead in either time or the number of logic ions. Here we report a quantum algorithmic readout whose overhead scales logarithmically with the number of clock ions in both of these respects. We show that the readout algorithm can be implemented with a single application of a multi-species quantum gate, which we describe in detail for a crystal of Aluminum and Calcium ions.

We demonstrate that it is possible, with sub-micron precision, to locate the absolute center of a Fabry-Pérot resonator oriented along the rf-field-free axis of a linear Paul trap through the application of two simultaneously resonating optical fields. In particular, we apply a probe field, which is near-resonant with an electronic transition of trapped ions, simultaneously with an off-resonant strong field acting as a periodic AC Stark-shifting potential. Through the resulting spatially modulated fluorescence signal we can find the cavity center of an 11.7 mm-long symmetric Fabry- Pérot cavity with a precision of $\pm$135 nm, which is smaller than the periodicity of the individual standing wave fields. This can e.g. be used to position the minimum of the axial trap potential with respect to the center of the cavity at any location along the cavity mode.

Precision spectroscopy of atomic and molecular ions offers a window to new physics, but is typically limited to species with a cycling transition for laser cooling and detection. Quantum logic spectroscopy has overcome this limitation for species with long-lived excited states. Here, we extend quantum logic spectroscopy to fast, dipole-allowed transitions and apply it to perform an absolute frequency measurement. We detect the absorption of photons by the spectroscopically investigated ion through the photon recoil imparted on a co-trapped ion of a different species, on which we can perform efficient quantum logic detection techniques. This amplifies the recoil signal from a few absorbed photons to thousands of fluorescence photons. We resolve the line center of a dipole-allowed transition in 40Ca+ to 1/300 of its observed linewidth, rendering this measurement one of the most accurate of a broad transition. The simplicity and versatility of this approach enables spectroscopy of many previously inaccessible species.