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Register a new userRydberg spectrum of a single trapped Ca$^+$ ion: A Floquet analysis
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We compute the Rydberg spectrum of a single Ca$^+$ ion in a Paul trap by incorporating various internal and external coupling terms of the ion to the trap in the Hamiltonian. The coupling terms include spin-orbit coupling in Ca$^+$, charge (electron and ionic core) coupling to the radio frequency and static fields, ion-electron coupling in the Paul trap, and ion center-of-mass coupling. The electronic Rydberg states are precisely described by a one-electron model potential for e$^-$+Ca$^{2+}$, and accurate eigenenergies, quantum defect parameters, and static and tensor polarizabilities for a number of excited Rydberg states are obtained. The time-periodic rf Hamiltonian is expanded in the Floquet basis, and the trapping-field-broadened Rydberg lines are compared with recent observations of Ca$^+(23P)$ and Ca$^+(52F)$ Rydberg lines.
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We provide a comprehensive theoretical framework for describing the dynamics of a single trapped ion interacting with a neutral buffer gas, thus extending our previous studies on buffer-gas cooling of ions beyond the critical mass ratio [B. Holtkemeier et al., Phys. Rev. Lett. 116, 233003 (2016)]. By transforming the collisional processes into a frame, where the ions micromotion is assigned to the buffer gas atoms, our model allows one to investigate the influence of non-homogeneous buffer gas configurations as well as higher multipole orders of the radio-frequency trap in great detail. Depending on the neutral-to-ion mass ratio, three regimes of sympathetic cooling are identified which are characterized by the form of the ions energy distribution in equilibrium. We provide analytic expressions and numerical simulations of the ions energy distribution, spatial profile and cooling rates for these different regimes. Based on these findings, a method for actively decreasing the ions energy by reducing the spatial expansion of the buffer gas arises (Forced Sympathetic Cooling).
We provide a detailed theoretical and conceptual study of a planned experiment to excite Rydberg states of ions trapped in a Paul trap. The ultimate goal is to exploit the strong state dependent interactions between Rydberg ions to implement quantum information processing protocols and to simulate the dynamics of strongly interacting spin systems. We highlight the promises of this approach when combining the high degree of control and readout of quantum states in trapped ion crystals with the novel and fast gate schemes based on interacting giant Rydberg atomic dipole moments. We discuss anticipated theoretical and experimental challenges on the way towards its realization.
We describe rapid, random-access loading of a two-dimensional (2D) surface-electrode ion-trap array based on two crossed photo-ionization laser beams. With the use of a continuous flux of pre-cooled neutral atoms from a remotely-located source, we achieve loading of a single ion per site while maintaining long trap lifetimes and without disturbing the coherence of an ion quantum bit in an adjacent site. This demonstration satisfies all major criteria necessary for loading and reloading extensive 2D arrays, as will be required for large-scale quantum information processing. Moreover, the already high loading rate can be increased by loading ions in parallel with only a concomitant increase in photo-ionization laser power and no need for additional atomic flux.
Many ion species commonly used for laser-cooled ion trapping studies have a low-lying metastable 2D3/2 state that can become populated due to spontaneous emission from the 2P1/2 excited state. This requires a repumper laser to maintain the ion in the Doppler cooling cycle. Typically the 2D3/2 state, or some of its hyperfine components if the ion has nuclear spin, has a higher multiplicity than the upper state of the repumping transition. This can lead to dark states, which have to be destabilized by an external magnetic field or by modulating the polarization of the repumper laser. We propose using unpolarized, incoherent amplified spontaneous emission (ASE) to drive the repumping transition. An ASE source offers several advantages compared to a laser. It prevents the buildup of dark states without external polarization modulation even in zero magnetic field, it can drive multiple hyperfine transitions simultaneously, and it requires no frequency stabilization. These features make it very compact and robust, which is essential for the development of practical, transportable optical ion clocks. We construct a theoretical model for the ASE radiation, including the possibility of the source being partially polarized. Using 88Sr+ as an example, the performance of the ASE source compared to a single-mode laser is analyzed by numerically solving the eight-level density matrix equations for the involved energy levels. Finally a reduced three-level system is derived, yielding a simple formula for the excited state population and scattering rate, which can be used to optimize the experimental parameters. The required ASE power spectral density can be obtained with current technology.
We study the formation and destabilization of dark states in a single trapped 88Sr+ ion caused by the cooling and repumping laser fields required for Doppler cooling and fluorescence detection of the ion. By numerically solving the time-dependent density matrix equations for the eight-level system consisting of the sublevels of the 5s 2S1/2, 5p 2P1/2, and 4d 2D3/2 states, we analyze the different types of dark states and how to prevent them in order to maximize the scattering rate, which is crucial for both the cooling and the detection of the ion. The influence of the laser linewidths and ion motion on the scattering rate and the dark resonances is studied. The calculations are then compared with experimental results obtained with an endcap ion trap system located at the National Research Council of Canada and found to be in good agreement. The results are applicable also to other alkaline earth ions and isotopes without hyperfine structure.
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