Piet O. Schmidt

Characterization of the trap rf induced a.c. Zeeman shift is essential for achieving high accuracy in optical ion clocks. In this work, we demonstrate the experimental characterization of this shift using highly charged $\mathrm{Ca}^{14+}$. The transverse component of the a.c. magnetic field is measured using the Autler-Townes splitting of the equally-spaced Zeeman components of the $^{3}\mathrm{P}_1$ when the Zeeman splitting is close to resonance with the trap rf drive frequency. We observe the resulting modulation by performing quantum logic spectroscopy using the co-trapped $\mathrm{Be}^{+}$. The longitudinal component is measured from probing the $\mathrm{Be}^{+}$ magnetic field-insensitive hyperfine transition $|F=2,m_F=0 \rangle \rightarrow | F=1,m_F=0 \rangle$. We confirm the small influence of the a.c. Zeeman shift in highly charged ions. The employed techniques can easily be transferred to other multi-level atomic systems.

We report on the sympathetic cooling and Coulomb crystallization of xenon highly charged ions (HCIs) with laser-cooled Ca$^+$ ions. The HCIs are produced in a compact electron beam ion trap, then charge selected, decelerated, and finally injected into a cryogenic linear Paul trap. There, they are captured into $^{40}$Ca$^+$ Coulomb crystals, and co-crystallized within them, causing dark voids in their fluorescence images. Fine control over the number of trapped ions and HCIs allows us to realize mixed-species crystals with arbitrary ordering patterns. By investigating Xe$^{q+}$--Ca$^+$ strings, we confirm the HCI charge states, measure their lifetime and characterize the mixed-species motional modes. Our system effectively combines the established quantum control toolbox for Ca$^+$ with the rich set of atomic properties of Xe highly charged ions, providing a resourceful platform for optical frequency metrology, searches for signatures of new physics, and quantum information science.

Single ion optical clocks have shown systematic frequency uncertainties below $10^{-18}$, but typically require more than one week of averaging to achieve a corresponding statistical uncertainty. This time can be reduced with longer probe times, but comes at the cost of a higher time-dilation shift due to motional heating of the ions in the trap. We show that sympathetic ground-state cooling using electromagnetically-induced transparency (EIT) of an \Al clock ion via a co-trapped \Ca ion during clock interrogation suppresses the heating of the ions. \Al can be kept close to the motional ground state, independent from the chosen interrogation time, at a relative time dilation shift of $(-1.69\pm0.20)\times10^{-18}$. The \Ca cooling light introduces an additional light shift on the \Al clock transition of $(-9.27\pm 1.03)\times10^{-18}$. We project that the uncertainty of this light shift can be further reduced by nearly an order of magnitude. This sympathetic cooling enables seconds of interrogation time with $10^{-19}$ motional and cooling laser-induced uncertainties for \Al and can be employed in other ion clocks as well.

In quantum logic spectroscopy, internal transitions of trapped ions and molecules can be probed by measuring the motional displacement caused by an applied light field of variable frequency. This provides a solution to ``needle in a haystack'' problems, such as the search for narrow clock transitions in highly charged ions, recently discussed by S. Chen et al. (Phys. Rev. Applied 22, 054059). The main bottleneck is the search speed over a frequency bandwidth, which can be increased by enhancing the sensitivity of displacement detection. In this work, we explore two complementary improvements: the use of squeezed motional states, explained using an analytical phase space model and optimal statistical postprocessing of data using a hypothesis testing framework. We demonstrate that each method independently provides a substantial boost to search speed. Their combination effectively mitigates state preparation and measurement errors, improving the search speed by an order of magnitude and fully leveraging the quantum enhancement offered by squeezing.

We measured the $g$-factor of the excited state $^3\text{P}_1$ in $\text{Ca}^{14+}$ ion to be $g = 1.499032(6)$ with a relative uncertainty of $4\times10^{-6}$. The magnetic field magnitude is derived from the Zeeman splitting of a $\text{Be}^+$ ion, co-trapped in the same linear Paul trap as the highly charged $\text{Ca}^{14+}$ ion. Furthermore, we experimentally determined the second-order Zeeman coefficient $C_2$ of the $^3\text{P}_0$ - $^3\text{P}_1$ clock transition. For the $m_J=0\rightarrow m_{J'}=0$ transition, we obtain $C_2 = 0.39\pm0.04\text{HzmT}^{-2}$, which is to our knowledge the smallest reported for any atomic transition to date. This confirms the predicted low sensitivity of highly charged ions to higher-order Zeeman effects, making them ideal candidates for high-precision optical clocks. Comparison of the experimental results with our state-of-the art electronic structure calculations shows good agreement, and demonstrates the significance of the frequency-dependent Breit contribution, negative energy states and QED effects on magnetic moments.

Recent advances in high-precision spectroscopy of highly charged ions necessitate an understanding of energy shifts of ionic levels caused by external electric and magnetic fields. Beyond the well-known Stark and linear Zeeman shifts, trapped ions may also exhibit quadratic Zeeman and electric quadrupole shifts. In this contribution, we present a systematic approach for the theoretical analysis of these shifts for arbitrary many-electron ions. Based on the derived expressions and making use of the multiconfigurational Dirac-Fock approach, we performed calculations of quadratic Zeeman shift coefficients and quadrupole moments for various ionic states in Ca$^{14+}$, Ni$^{12+}$ and Xe$^{q+}$ ions. These ions attract particular interest for ongoing and future experiments in optical clocks and tests of fundamental physics.

Extending quantum control to increasingly complex systems is crucial for both advancing quantum technologies and fundamental physics. In trapped ion systems, quantum logic techniques that combine a well-controlled logic species with a more complex spectroscopy species have proven to be a powerful tool for extending the range of accessible species. Here, we demonstrate that a quantum system as complex as $^{48}$Ti$^+$ with its many metastable states can be controlled employing a combination of intrinsic thermalization due to collisions with background gas and quantum-logic techniques using a far-detuned Raman laser. The preparation of pure quantum states allows coherent manipulation and high resolution measurements of the Zeeman structure in $^{48}$Ti$^+$. The presented techniques are applicable to a wide range of ionic species giving access to a larger variety of systems for fundamental physics and constitute the first step for quantum-controlled spectroscopy of transition metals, relevant, e.g., for the interpretation of astrophysical spectra.

The demand for efficient preparation methods for dual-species ion crystals is rapidly expanding across quantum technology and fundamental physics applications with trapped ions. We present a deterministic and efficient technique to produce such crystals, utilizing the segmented structure of a linear Paul trap. By precisely tailoring the trapping potentials, we can split, move, and discard parts of an ion chain. This process is automated in a sequence that converts a larger ion sample into the desired configuration. A critical component of our approach is the accurate identification of crystal constituents. This is achieved by matching the measured positions of fluorescing ions against theoretical expectations for larger crystals, thus facilitating the detection of non-fluorescing ions and enabling accurate ion counting. We demonstrate that our method reliably produces two-ion crystals within minutes. These results represent a significant advance in the production of two-species ion crystals with applications ranging from quantum logic spectroscopy and optical clocks to quantum computing and simulation with trapped ions.

We present the experimental realization of a continuous dynamical decoupling scheme which suppresses leading frequency shifts in a multi-ion frequency reference based on $^{40}\mathrm{Ca}^+$. By near-resonant magnetic coupling of the $^2\mathrm{S}_{1/2}$ and $^2\mathrm{D}_{5/2}$ Zeeman sub-levels using radio-frequency dressing fields, engineered transitions with reduced sensitivity to magnetic-field fluctuations are obtained. A second stage detuned dressing field reduces the influence of amplitude noise in the first stage driving fields and decreases 2\textsuperscript{nd}-rank tensor shifts, such as the electric quadrupole shift. Suppression of the quadratic dependence of the quadrupole shift to $3(2)\,\text{mHz}/μm^2$ and coherence times of $290(20)\,\text{ms}$ on the optical transition are demonstrated even within a laboratory environment with significant magnetic field noise. Besides removing inhomogeneous line shifts in multi-ion clocks, the demonstrated dynamical decoupling technique may find applications in quantum computing and simulation with trapped ions by a tailored design of decoherence-free subspaces.

Lasers with high spectral purity are indispensable for optical clocks and coherent manipulation of atomic and molecular qubits for applications such as quantum computing and quantum simulation. Stabilisation of the laser to a reference can provide a narrow linewidth and high spectral purity. However, widely-used diode lasers exhibit fast phase noise that prevents high fidelity qubit manipulation. Here we demonstrate a self-injection locked diode laser system utilizing a medium finesse cavity. The cavity not only provides a stable resonance frequency, but at the same time acts as a low-pass filter for phase noise beyond the cavity linewidth of around 100 kHz, resulting in low phase noise from dc to the injection lock limit. We model the expected laser performance and benchmark it using a single trapped $^{40}$Ca$^{+}$-ion as a spectrum analyser. We show that the fast phase noise of the laser at relevant Fourier frequencies of 100 kHz to >2 MHz is suppressed to a noise floor of between -110 dBc/Hz and -120 dBc/Hz, an improvement of 20 to 30 dB over state-of-the-art Pound-Drever-Hall-stabilized extended-cavity diode lasers. This strong suppression avoids incoherent (spurious) spin flips during manipulation of optical qubits and improves laser-driven gates in using diode lasers with applications in quantum logic spectroscopy, quantum simulation and quantum computation.

We implement sympathetic cooling of highly charged ions (HCI) by fully enclosing a linear Paul trap within a superconducting radio-frequency resonator. A quantization magnetic field applied while cooling down into the superconducting state remains present in the trap for centuries and external electromagnetic fluctuations are greatly suppressed. A magnetic field decay rate at the 10$^{-10}$ s$^{-1}$ level is found using trapped Doppler-cooled Be$^+$ ions as hyperfine-structure (hfs) qubits. Ramsey interferometry and spin-echo measurements on magnetically-sensitive hfs transitions yield coherence times of >400 ms, showing excellent passive shielding at frequencies down to DC. For sympathetic cooling of HCI, we extract them from an electron beam ion trap (EBIT) and co-crystallize one together with Doppler-cooled Be$^+$ ions. By subsequently ejecting all but one Be$^+$ ions, we prepare single HCI for quantum logic spectroscopy towards frequency metrology and qubit operations with a great variety of HCI species.

Most ions lack the fast, cycling transitions that are necessary for direct laser cooling. In most cases, they can still be cooled sympathetically through their Coulomb interaction with a second, coolable ion species confined in the same potential. If the charge-to-mass ratios of the two ion types are too mismatched, the cooling of certain motional degrees of freedom becomes difficult. This limits both the achievable fidelity of quantum gates and the spectroscopic accuracy. Here we introduce a novel algorithmic cooling protocol for transferring phonons from poorly- to efficiently-cooled modes. We demonstrate it experimentally by simultaneously bringing two motional modes of a Be$^{+}$-Ar$^{13+}$ mixed Coulomb crystal close to their zero-point energies, despite the weak coupling between the ions. We reach the lowest temperature reported for a highly charged ion, with a residual temperature of only $T\lesssim200~\mathrm{μK}$ in each of the two modes, corresponding to a residual mean motional phonon number of $\langle n \rangle \lesssim 0.4$. Combined with the lowest observed electric field noise in a radiofrequency ion trap, these values enable an optical clock based on a highly charged ion with fractional systematic uncertainty below the $10^{-18}$ level. Our scheme is also applicable to (anti-)protons, molecular ions, macroscopic charged particles, and other highly charged ion species, enabling reliable preparation of their motional quantum ground states in traps.

Precision spectroscopy has been the driving force for progress of our physical understanding and still is a promising tool for the investigation of new physics. Molecules offer transitions which allow tests that are not possible in atomic systems. However, usually precision spectroscopy of molecules is challenging due to the lack of cycling transitions for state preparation and state detection. For molecular ions, this obstacle can be overcome by quantum logic spectroscopy, where dissipation for state preparation and detection is provided by a co-trapped atomic ion exploiting the shared eigenstates of motion. Here, we propose a full quantum logic spectroscopy scheme for molecular oxygen ions and theoretically investigate the feasibility of quantum logic assisted state detection and preparation. Furthermore, we provide coupling rates for a direct single-photon quadrupole excitation of a vibrational overtone transition that can serve as a sensitive transition for tests of a possible variation of the proton-to-electron mass ratio.

There has been tremendous progress in the performance of optical frequency standards since the first proposals to carry out precision spectroscopy on trapped, single ions in the 1970s. The estimated fractional frequency uncertainty of today's leading optical standards is currently in the $10^{-18}$ range, approximately two orders of magnitude better than that of the best caesium primary frequency standards. This exceptional accuracy and stability is resulting in a growing number of research groups developing optical clocks. While good review papers covering the topic already exist, more practical guidelines are needed as a complement. The purpose of this document is therefore to provide technical guidance for researchers starting in the field of optical clocks. The target audience includes national metrology institutes (NMIs) wanting to set up optical clocks (or subsystems thereof) and PhD students and postdocs entering the field. Another potential audience is academic groups with experience in atomic physics and atom or ion trapping, but with less experience of time and frequency metrology and optical clock requirements. These guidelines have arisen from the scope of the EMPIR project "Optical clocks with $1 \times 10^{-18}$ uncertainty" (OC18). Therefore, the examples are from European laboratories even though similar work is carried out all over the world. The goal of OC18 was to push the development of optical clocks by improving each of the necessary subsystems: ultrastable lasers, neutral-atom and single-ion traps, and interrogation techniques. This document shares the knowledge acquired by the OC18 project consortium and gives practical guidance on each of these aspects.

A cryogenic radio-frequency ion trap system designed for quantum logic spectroscopy of highly charged ions is presented. It includes a segmented linear Paul trap, an in-vacuum imaging lens and a helical resonator. We demonstrate ground state cooling of all three modes of motion of a single $^9$Be$^+$ ion and determine their heating rates as well as excess axial micromotion. The trap shows one of the lowest levels of electric field noise published to date. We investigate the magnetic-field noise suppression in cryogenic shields made from segmented copper, the resulting magnetic field stability at the ion position and the resulting coherence time. Using this trap in conjunction with an electron beam ion trap and a deceleration beamline, we have been able to trap single highly charged Ar$^{13+}$ (Ar XIV) ions concurrently with single Be$^+$ ions, a key prerequisite for the first quantum logic spectroscopy of a highly charged ion.

Simulating computationally intractable many-body problems on a quantum simulator holds great potential to deliver insights into physical, chemical, and biological systems. While the implementation of Hamiltonian dynamics within a quantum simulator has already been demonstrated in many experiments, the problem of initialization of quantum simulators to a suitable quantum state has hitherto remained mostly unsolved. Here, we show that already a single dissipatively driven auxiliary particle can efficiently prepare the quantum simulator in a low-energy state of largely arbitrary Hamiltonians. We demonstrate the scalability of our approach and show that it is robust against unwanted sources of decoherence. While our initialization protocol is largely independent of the physical realization of the simulation device, we provide an implementation example for a trapped ion quantum simulator.

We present a multilayer surface-electrode ion trap with embedded 3D microwave circuitry for implementing entangling quantum logic gates. We discuss the electromagnetic full-wave simulation procedure that has led to the trap design and the characterization of the resulting microwave field-pattern using a single ion as a local field probe. The results agree with simulations within the uncertainty; compared to previous traps, this design reduces detrimental AC Zeeman shifts by three orders of magnitude. The design presented here can be viewed as an entangling gate component in a library for surface-electrode ion traps intended for quantum logic operations.

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.

In photon recoil spectroscopy, signals are extracted from recoils imparted by the spectroscopy light on the motion of trapped ions as demonstrated by C. Hempel et al., Nature Photonics 7, 630 (2013) and Y. Wan et al., Nature Communications 5, 3096 (2014). The method exploits the exquisite efficiency in the detection of phonons achievable in ion crystals, and is thus particularly suitable for species with broad non-cycling transitions where detection of fluorescence photons is impractical. Here, we develop a theoretical model for the description of photon recoil spectroscopy based on a Fokker-Planck equation for the Wigner function of the phonon mode. Our model correctly explains systematic shifts due to Doppler heating and cooling as observed in the experiment. Furthermore, we investigate quantum metrological schemes for enhancing the spectroscopic sensitivity based on the preparation and detection of nonclassical states of the phonon mode.

Non-vanishing fluctuations of the vacuum state are a salient feature of quantum theory. These fluctuations fundamentally limit the precision of quantum sensors. Nowadays, several systems such as optical clocks, gravitational wave detectors, matter-wave interferometers, magnetometers, and optomechanical systems approach measurement sensitivities where the effect of quantum fluctuations sets a fundamental limit, the so-called standard quantum limit (SQL). It has been proposed that the SQL can be overcome by squeezing the vacuum fluctuations. Realizations of this scheme have been demonstrated in various systems. However, protocols based on squeezed vacuum crucially rely on precise control of the relative orientation of the squeezing with respect to the operation imprinting the measured quantity. Lack of control can lead to an amplification of noise and reduces the sensitivity of the device. Here, we experimentally demonstrate a novel quantum metrological paradigm based on phase insensitive Fock states of the motional state of a trapped ion, with applications in frequency metrology and displacement detection. The measurement apparatus is used in two different experimental settings probing non-commuting observables with sensitivities beyond the SQL. In both measurements, classical preparation and detection noise are sufficiently small to preserve the quantum gain in a full metrological protocol.

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.

Efficient preparation and detection of the motional state of trapped ions is important in many experiments ranging from quantum computation to precision spectroscopy. We investigate the stimulated Raman adiabatic passage (STIRAP) technique for the manipulation of motional states in a trapped ion system. The presented technique uses a Raman coupling between two hyperfine ground states in $^{25}$Mg$^+$, implemented with delayed pulses, which removes a single phonon independent of the initial motional state. We show that for a thermal state the STIRAP population transfer is more efficient than a stimulated Raman Rabi pulse on a motional sideband. In contrast to previous implementations, a large detuning of more than 200 times the natural linewidth of the transition is used. This approach renders STIRAP suitable for atoms in which resonant laser fields would populate fluorescing excited states and thus impede the STIRAP process. We use the technique to measure the wavefunction overlap of excited motional states with the motional ground state. This is an important application for photon recoil spectroscopy and other force sensing applications that utilize the high sensitivity of the motional state of trapped ions to external fields. Furthermore, a determination of the ground state population enables a simple measurement of the ion's temperature.

Laser spectroscopy of cold and trapped molecular ions is a powerful tool for fundamental physics, including the determination of fundamental constants, the laboratory test for their possible variation, and the search for a possible electric dipole moment of the electron. Optical clocks based on molecular ions sensitive to some of these effects are expected to achieve uncertainties approaching the $10^{-18}$ level. While the complexity of molecular structure facilitates these applications, the absence of cycling transitions poses a challenge for direct laser cooling, quantum state control, and detection. Previously employed state detection techniques based on photo-dissociation or chemical reactions are destructive and therefore inefficient. Here we experimentally demonstrate non-destructive state detection of a single trapped molecular ion through its strong Coulomb coupling to a well-controlled co-trapped atomic ion. An algorithm based on a state-dependent optical dipole force(ODF) changes the internal state of the atom conditioned on the internal state of the molecule. We show that individual states in the molecule can be distinguished by their coupling strength to the ODF and observe black-body radiation-induced quantum jumps between rotational states. Using the detuning dependence of the state detection signal, we implement a variant of quantum logic spectroscopy and improve upon a previous measurement of the $\mathrm{X}^1Σ^+(J=1)\rightarrow\mathrm{A}^1Σ^+(J=0)$ transition in MgH, finding a frequency of 1067.74752(53)THz. We estimate that non-destructive state detection with near 100% efficiency could take less than 10 ms. The technique we demonstrate is applicable to a wide range of molecular ions, enabling further applications in state-controlled quantum chemistry and spectroscopic investigations of molecules serving as probes for interstellar clouds.

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.

We demonstrate an efficient high-precision optical spectroscopy technique for single trapped ions with non-closed transitions. In a double-shelving technique, the absorption of a single photon is first amplified to several phonons of a normal motional mode shared with a co-trapped cooling ion of a different species, before being further amplified to thousands of fluorescence photons emitted by the cooling ion using the standard electron shelving technique. We employ this extension of the photon recoil spectroscopy technique to perform the first high precision absolute frequency measurement of the $^{2}$D$_{3/2}$ $\rightarrow$ $^{2}$P$_{1/2}$ transition in $^{40}$Ca$^{+}$, resulting in a transition frequency of $f=346\, 000\, 234\, 867(96)$ kHz. Furthermore, we determine the isotope shift of this transition and the $^{2}$S$_{1/2}$ $\rightarrow$ $^{2}$P$_{1/2}$ transition for $^{42}$Ca$^{+}$, $^{44}$Ca$^{+}$ and $^{48}$Ca$^{+}$ ions relative to $^{40}$Ca$^{+}$ with an accuracy below 100 kHz. Improved field and mass shift constants of these transitions as well as changes in mean square nuclear charge radii are extracted from this high resolution data.

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.

Optical atomic clocks represent the state-of-the-art in the frontier of modern measurement science. In this article we provide a detailed review on the development of optical atomic clocks that are based on trapped single ions and many neutral atoms. We discuss important technical ingredients for optical clocks, and we present measurement precision and systematic uncertainty associated with some of the best clocks to date. We conclude with an outlook on the exciting prospect for clock applications.

We present and characterize fiber mirrors and a miniaturized ion-trap design developed to integrate a fiber-based Fabry-Perot cavity (FFPC) with a linear Paul trap for use in cavity-QED experiments with trapped ions. Our fiber-mirror fabrication process not only enables the construction of FFPCs with small mode volumes, but also allows us to minimize the influence of the dielectric fiber mirrors on the trapped-ion pseudopotential. We discuss the effect of clipping losses for long FFPCs and the effect of angular and lateral displacements on the coupling efficiencies between cavity and fiber. Optical profilometry allows us to determine the radii of curvature and ellipticities of the fiber mirrors. From finesse measurements we infer a single-atom cooperativity of up to $12$ for FFPCs longer than $200 μ$m in length; comparison to cavities constructed with reference substrate mirrors produced in the same coating run indicates that our FFPCs have similar scattering losses. We discuss experiments to anneal fiber mirrors and explore the influence of the atmosphere under which annealing occurs on coating losses, finding that annealing under vacuum increases the losses for our reference substrate mirrors. Our unique linear Paul trap design provides clearance for such a cavity and is miniaturized to shield trapped ions from the dielectric fiber mirrors. We numerically calculate the trap potential in the absence of fibers. In the experiment additional electrodes can be used to compensate distortions of the potential due to the fibers. Home-built fiber feedthroughs connect the FFPC to external optics, and an integrated nanopositioning system affords the possibility of retracting or realigning the cavity without breaking vacuum.

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.

Sympathetic cooling of trapped ions has become an indispensable tool for quantum information processing and precision spectroscopy. In the simplest situation a single Doppler-cooled ion sympathetically cools another ion which typically has a different mass. We analytically investigate the effect of the mass ratio of such an ion crystal on the achievable temperature limit in the presence of external heating. As an example, we show that cooling of a single Al+ with Be+, Mg+ and Ca+ ions provides similar results for heating rates typically observed in ion traps, whereas cooling ions with a larger mass perform worse. Furthermore, we present numerical simulation results of the rethermalisation dynamics after a background gas collision for the Al+/Ca+ crystal for different cooling laser configurations.

Protocols used in quantum information and precision spectroscopy rely on efficient internal quantum state discrimination. With a single ion in a linear Paul trap, we implement a novel detection method which utilizes correlations between two detection events with an intermediate spin-flip. The technique is experimentally characterized as more robust against fluctuations in detection laser power compared to conventionally implemented methods. Furthermore, systematic detection errors which limit the Rabi oscillation contrast in conventional methods are overcome.

We prove an uncertainty relation for energy and arrival time, where the arrival of a particle at a detector is modeled by an absorbing term added to the Hamiltonian. In this well-known scheme the probability for the particle's arrival at the counter is identified with the loss of normalization for an initial wave packet. Under the sole assumption that the absorbing term vanishes on the initial wave function, we show that $ΔT ΔE \geq \sqrt p \hbar/2$ and $<T> ΔE\geq 1.37\sqrt p\hbar$, where $<T>e$ denotes the mean arrival time, and $p$ is the probability for the particle to be eventually absorbed. Nearly minimal uncertainty can be achieved in a two-level system, and we propose a trapped ion experiment to realize this situation.

We present a single solid-state laser system to cool, coherently manipulate and detect $^{25}$Mg$^+$ 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.