Michael Drewsen

Ion Coulomb crystals are ordered structures formed by laser-cooled ions in traps that are characterized by interparticle distances of several micrometers and energy scales on the order of $μ$eV. Their crystalline structure emerges from the interplay between Coulomb repulsion and the external confining potential, which can be readily tuned. Moreover, individual ions can be precisely manipulated with lasers and imaged via resonance fluorescence. These unusual and unique properties make ion crystals a powerful platform for studying phases of matter in the strongly correlated regime and at low temperatures where their dynamics is manifestly quantum mechanical. This review examines the theoretical framework and experimental characterization of ion Coulomb crystals from a condensed-matter perspective. We discuss their dynamical and thermodynamic properties in one, two, and three dimensions, and review recent investigations into their out-of-equilibrium behavior. We provide outlooks on future directions for exploring novel condensed matter phenomena with trapped ion crystals, as well as for exploiting these features for scientific and technical applications.

In the study of ion-atom interactions, the ion often remain trapped during the experiments. However, the effects of the trapping potential of the ion on ion-neutral interactions remain largely unexplored. Although trap-assisted ion-neutral complex formation has been experimentally studied and described by applying semiclassical theories where the ion is treated as a point charge particle, the potential effect of a delocalized charge distribution of a confined ion due to its quantum mechanical wavefunction has not been considered. To remedy this, in the present theoretical work we substitute the point charge of the ion with a delocalized charged distribution according to its motional ground state in the trap. Our results show that the trapping frequency and hence the spatial extension of the ion's ground-state wavefunction drastically affects the elastic and transport cross sections in interactions with neutral atoms. Stimulated by these results, we propose experimental procedures to verify the effects of the delocalize charge distribution in ion-atom interactions via measuring the heating rate of the ion due to the energy transfer in atomic collisions. Our novel approach brings new possibilities for investigating ion-neutral systems and, through them, new perspectives on ionic polarons and potentially a better understanding of trap-induced losses in ion-neutral experiments.

Sympathetic cooling of molecular ions through the Coulomb interaction with laser-cooled atomic ions is an efficient tool to prepare translationally cold molecules without, ideally, affecting the internal state of the molecular ions. However, the electric field due to the Coulomb interaction may induce rotational transitions that change the purity of initially quantum state prepared molecules. Here, we use estimates of rotational state changes in single collisions of diatomic ions with atomic ions [arXiv:1905.02130] to determine the overall rotational excitation accumulated over the sympathetic cooling. Considering two different experimental scenarios, that of a molecular ion co-trapped with a single atomic ion and a molecular ion immersed in a Coulomb crystal of atomic ions, we also estimate the cooling time.

In the last decade, a growing interest has been devoted to models of spontaneous collapse of the wavefunction, known also as collapse models. They coherently solve the well-known quantum measurement problem by suitably modifying the Schrödinger evolution. Quantum experiments are now finally within the reach of testing such models (and thus testing the limits of quantum theory). Here, we propose a method based on a two-ions confined in a linear Paul trap to possibly enhance the testing capabilities of such experiments. The combination of an atomic and a macromolecular ion provide a good match for the cooling of the motional degrees of freedom and a non-negligible insight in the collapse mechanism, respectively.

We explore the interaction between two trapped ions mediated by a surrounding quantum degenerate Bose or Fermi gas. Using perturbation theory valid for weak atom-ion interaction, we show analytically that the interaction mediated by a Bose gas has a power-law behaviour for large distances whereas it has a Yukawa form for intermediate distances. For a Fermi gas, the mediated interaction is given by a power-law for large density and by a Ruderman-Kittel-Kasuya-Yosida form for low density. For strong atom-ion interactions, we use a diagrammatic theory to demonstrate that the mediated interaction can be a significant addition to the bare Coulomb interaction between the ions, when an atom-ion bound state is close to threshold. Finally, we show that the induced interaction leads to substantial and observable shifts in the ion phonon frequencies.

We reflect on the prospect of exploiting the recoil associated with absorption and emission of photons to perform spectroscopy of a single molecular ion. For this recoil to be detectable, the molecular ion is sympathetically cooled by a laser-cooled atomic ion to near their common quantum mechanical ground state within a trapping potential. More specifically, we present a general framework for simulating the expected photon recoil spectra in regimes where either the natural transition linewidth $Γ_t$ of the molecular ion or the spectral width $Γ_L$ of the exciting light source exceeds the motional frequencies of the two-ion system. To exemplify the framework, we present two complementary cases: spectroscopy of the broad 3s $^2$S$_{1/2}$ - 3p $^2$P$_{3/2}$ electronic transition ($Γ_t/2π= 41.8$ MHz) of a single $^{24}$Mg$^+$ ion at $λ=279.6$ nm by a narrow laser source ($Γ_L/2π\lesssim 1$ MHz) and mid-infrared vibrational spectroscopy of the very narrow $|v=0,J=1\rangle$ - $|v'=1,J'=0\rangle$ transition ($Γ_t/2π= 2.50 $ Hz) at $λ=6.17$ $μ$m in the $^1Σ^+$ electronic ground state of $^{24}$MgH$^+$ by a broadband laser source ($Γ_L/2π\gtrsim$ 50 MHz). The atomic ion $^{24}$Mg$^+$ has been picked to introduce a simple system to make comparisons with experimental results while still capturing most of the physics involved in electronic excitations of molecular ions.

We demonstrate the use of a femtosecond frequency comb to coherently drive stimulated Raman transitions between terahertz-spaced atomic energy levels. More specifically, we address the $3d~^2D_{3/2}$ and $3d~^2D_{5/2}$ fine structure levels of a single trapped $^{40}$Ca$^+$ ion and spectroscopically resolve the transition frequency to be $ν_D = 1{,}819{,}599{,}021{,}534 \pm 8$ Hz. The achieved accuracy is nearly a factor of five better than the previous best Raman spectroscopy, and is currently limited by the stability of our atomic clock reference. Furthermore, the population dynamics of frequency-comb-driven Raman transitions can be fully predicted from the spectral properties of the frequency comb, and Rabi oscillations with a contrast of 99.3(6)\% and millisecond coherence time has been achieved. Importantly, the technique can be easily generalized to transitions in the sub-kHz to tens of THz range and should be applicable for driving, e.g., spin-resolved rovibrational transitions in molecules and hyperfine transitions in highly charged ions.

A Ramsey-type interferometer is suggested, employing a cold trapped ion and two time-delayed off-resonant femtosecond laser pulses. The laser light couples to the molecular polarization anisotropy, inducing rotational wavepacket dynamics. An interferogram is obtained from the delay dependent populations of the final field-free rotational states. Current experimental capabilities for cooling and preparation of the initial state are found to yield an interferogram visibility of more than 80\%. The interferograms can be used to determine the polarizability anisotropy with an accuracy of about $\pm 2\%$, respectively $\pm 5\%$, provided the uncertainty in the initial populations and measurement errors are confined to within the same limits.

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.

We present experimental results on adiabatic cooling of a single 40Ca+ ion in a linear radiofrequency trap. After a period of laser cooling, the secular frequency along the rf-field-free axis is adiabatically lowered by nearly a factor of eight from 583 kHz to 75 kHz. For an ion originally Doppler laser cooled to a temperature of 0.65 +/- 0.03 mK, a temperature of 87 +/- 7 μK is measured after the adiabatic expansion. Applying the same adiabatic cooling procedure to a single sideband cooled ion in the ground state (P0 = 0.978 +/- 0.002) resulted in a final ground state occupation of 0.947 +/- 0.005. Both results are in excellent agreement with an essentially fully adiabatic behavior. The results have a wide range of perspectives within such diverse fields as ion based quantum information science, high resolution molecular ion spectroscopy and ion chemistry at ultra-low temperatures.

We present a method for determining the 3D intensity distribution of directed laser radiation with micrometer resolution in restricted volumes. Our method is based on in-coupling and guiding properties of optical fibers, with the current version requiring only few hundred micrometers. We characterize the performance of the method and experimentally demonstrate profiling of micrometer sized laser beams. We discuss the limiting factors and routes towards a further increase of the resolution and beam profiling in even more restricted volumes. Finally, as an application example, we present profiling of laser beams inside a micro ion trap with integrated optical fibers.

We demonstrate experimentally how the process of Stimulated Raman Adiabatic Passage (STIRAP) can be utilized for efficient coherent internal state transfer in single trapped and laser-cooled $^{40}$Ca$^+$ ions. The transfer from the D$_{3/2}$ to the D$_{5/2}$ state, is detected by a fluorescence measurement revealing the population not transfered to the D$_{5/2}$ state. A coherent population transfer efficiency at the level of 95 % in a setup allowing for the internal state detection of individual ions in a string has been obtained.

With MgH^+ ions as a test case, we investigate to what extent the rotational motion of smaller polar molecular ions sympathetically cooled into Coulomb crystals in linear Paul traps couples to the translational motions of the ion ensemble. By comparing results obtained from rotational state-selective resonance-enhanced photo-dissociation experiments with data from theoretical simulations, we conclude that the effective rotational temperature exceeds the translational temperature (< 100 mK) by more than two orders of magnitude, indicating a very weak coupling. In fact, the experimental results are consistent with the rotational temperature being in thermal equilibrium with the surrounding environment at ~300 K.

We present an implementation of quantum logic gates via internal state dependent displacements of ions in a linear Paul trap caused by optical dipole forces. Based on a general quantum analysis of the system dynamics we consider specific implementations with alkaline earth ions. For experimentally realistic parameters gate infidelities as low as $10^{-4}$ can be obtained.

We present a measurement of the lifetime of the metastable 3d 2D5/2 state in the 40Ca+ ion, using the so-called shelving technique on a string of five Doppler laser-cooled ions in a linear Paul trap. A detailed account of the data analysis is given, and systematic effects due to unwanted excitation processes and collisions with background gas atoms are discussed and estimated. From a total of 6805 shelving events, we obtain a lifetime tau=1149+/-14(stat.)+/-4(sys.)ms, a result which is in agreement with the most recent measurements.

We present a scheme utilizing position-dependent ac Stark shifts for doing quantum logic with trapped ions. By a proper choice of direction, position and size, as well as power and frequency of a far-off-resonant Gaussian laser beam, specific ac Stark shifts can be assigned to the individual ions, making them distinguishable in frequency-space. In contrast to previous all-optical based quantum gates with trapped ions, the present scheme enables individual addressing of single ions and selective addressing of any pair of ions for two-ion quantum gates, without using tightly focused laser beams. Furthermore, the decoherence rate due to off-resonant excitations can be made negligible as compared with other sources of decoherence.