Rare calcium isotope 43Ca+ ion (0.135%) is the only naturally abundant isotope with hyperfine structure. This isotope is considered an attractive candidate both for an optical frequency standard and for quantum information processing. We report a method to load 43Ca+ ions selectively into a linear Paul trap using a two-step, resonant photo-ionization process. Isotope selectivity is achieved by utilizing the isotope shifts for the resonant 4s2 1S0-4s4p 1P1 transition of neutral calcium. The second non-resonant excitation is achieved by an ultraviolet light emitting diode (LED). The use of an LED is simpler and more economical than using a laser for the second transition. Additionally the laser cooling of 43Ca+ is demonstrated using two ultraviolet-diode lasers and two infrared-diode lasers. Due to the hyperfine structure, the laser requirements for Doppler cooling 43Ca+ are more demanding than for the other isotopes.
Rare calcium isotope 43Ca+ ion (0.135%) is the only naturally abundant isotope with hyperfine structure. This isotope is considered an attractive candidate both for an optical frequency standard and for quantum information processing. We report a method to load 43Ca+ ions selectively into a linear Paul trap using a two-step, resonant photo-ionization process. Isotope selectivity is achieved by utilizing the isotope shifts for the resonant 4s2 1S0-4s4p 1P1 transition of neutral calcium. The second non-resonant excitation is achieved by an ultraviolet light emitting diode (LED). The use of an LED is simpler and more economical than using a laser for the second transition. Additionally the laser cooling of 43Ca+ is demonstrated using two ultraviolet-diode lasers and two infrared-diode lasers. Due to the hyperfine structure, the laser requirements for Doppler cooling 43Ca+ are more demanding than for the other isotopes.
We present studies of resonance-enhanced photoionization for isotope-selective loading of Ca+ into a Paul trap. The ${4s}^{2}{}^{1}{S}_{0}\ensuremath{\leftrightarrow}4s4p{}^{1}{P}_{1}$ transition of neutral calcium is driven by a 423 nm laser and the atoms are photoionized by a second laser at 389 nm. Isotope selectivity is achieved by using crossed atomic and laser beams to reduce the Doppler width significantly below the isotope shifts in the 423 nm transition. The loading rate of ions into the trap is studied under a range of experimental parameters for the abundant isotope 40Ca+. Using the fluorescence of the atomic beam at 423 nm as a measure of the Ca number density, we estimate a lower limit for the absolute photoionization cross section of 170(60) Mb. We achieve loading and laser cooling of all the naturally occurring isotopes, without the need for enriched sources. Laser heating/cooling is observed to enhance the isotope selectivity. In the case of the rare species 43Ca+ and 46Ca+, which have not previously been laser cooled, the loading is not fully isotope selective, but we show that pure crystals of 43Ca+ may nevertheless be obtained. We find that for loading 40Ca+ the 389 nm laser may be replaced by an incoherent source.
In this paper, we present a detailed method for rapidly and effectively loading a single 40 Ca + ion into a miniature linear Paul trap. Calcium atoms are generated by laser ablation, and the single ion is loaded and specific isotopes are selected by a two-step photo-ionization method. Compared to the traditional photo-ionization method in which atoms are typically emitted from a resistively heated oven, the advantages of laser ablation are that it can be precisely controlled, it can effectively avoid the problem of fluxed calcium deposition on the trap electrodes, and it restricts the generation of dark ions, which can influence atomic-precision spectroscopy measurements. With its short loading time, it is possible to load an ion in few seconds with the appropriate parameters. The technique of laser ablation has been applied to generate several species of atoms and ions at present, it will potentially benefit in the studies of optical frequency standards, quantum simulation and quantum information processing in an ultra-high vacuum condition and cryogenic system.
This thesis describes experimental work towards developing a trapped ion quantum information processor. An existing ion trap apparatus was capable of trapping and laser-cooling single ions or small ion strings of 40 Ca+, and had been used for studies of quantum jumps and natural lifetime measurements in Ca. This thesis describes improvements in this apparatus, which have allowed the stability and the flexibility of experimental control of the ions to be greatly increased. This enabled experiments to read out the spin state of a single trapped ion, and to load ions with isotope selectivity through photoionization. The optical systems were improved by installation of new lasers, optical reference cavities, and a system of acousto-optic modulators for laser intensity switching and frequency control. The photon counting for fluorescence detection was improved, and a new photon time-of-arrival correlation circuit developed. This has permitted rapid and more sensitive detection of micromotion, and hence cancellation of stray fields in the trap. A study of resonant circuits in the low RF, high voltage (10 MHz, 1 kV) regime was carried out with a view to developing a new RF supply for the Paul trap with reduced noise and increased power. A new supply based on a helical resonator was built and used to trap ions. This technique has reduced noise and will permit higher secular frequencies to be attained in the future. A magnetic field B in the ion trap is used to define a quantization axis, and in one series of experiments was required to be of order 100 G to provide a substantial Zeeman splitting. A set of magnetic field coils to control the size and direction of B is described. The design of these posed some problems owing to an unforseen issue with the vacuum chamber. In short, it is magnetizable and acts to first approximation like a magnetic shield. The field coils had to be sufficiently substantial to produce the desired field at the ion even in the presence of this shielding effect, and dark resonance (and other) spectra with Zeeman splitting were obtained to calibrate the field using the ion as a probe. Finally, the thesis describes the successful loading of the ion trap by laser photoionization from a weak atomic beam. This involved two new lasers at 423 nm and 389 nm. Saturated absorption spectroscopy of neutral calcium is first described, then transverse excitation of an atomic beam in our vacuum chamber is used to identify all the main isotopes of calcium and confirm their abundances in our source (a heated sample of natural calcium). Finally, photoionization is used to load the trap. This has three advantages over electron-impact ionization. By avoiding an electron gun, we avoid charging of insulating patches and subsequent electric field drift as they discharge; the flux in the atomic beam and hence calcium (and other) deposits on the electrodes can be greatly reduced; and most importantly, the photoionization is isotope selective. Evidence is presented which suggests that even with an non-enriched source, the rare isotope 43 Ca can be loaded with reasonable efficiency. This isotope is advantageous for quantum information experiments for several reasons, but chiefly because its ground state hyperfine structure can act as a stable qubit.
Trapped single ions provide an ideal platform for studying quantum optics, light-matter interactions, and quantum information processing. Many of these applications rely on the availability of well-defined and reproducible quantum emitters as well as precise control over the internal states of ions. To study both of these concepts, this thesis focuses on the isotope selectivity of neutral Barium (Ba) transitions as well as the state preparation of single trapped 138Ba+ ions. The first part of this thesis introduces the theoretical framework for experiments, focusing on single Ba+ ions and light-matter interactions. Therefore, the working principle of Paul traps is presented, the Ba ion is introduced and fundamental light-matter interaction tightly related to the experiments and simulations presented in this work are established. In the second part, the isotope selectivity of the neutral Ba 6s2 1S0 to 6s6p 1P1 transition at 553 nm is investigated and compared with the isotope selectivity of the 6s2 1S0 to 5d6p 3D1 transition at 413 nm. A secondary photon can be used in both cases to achieve isotope selective ionization of Ba+ ions. The isotope selectivity of the 553 nm transition was tested by carrying out spectroscopy and comparing the results with existing data. The isotope selectivity for other naturally available Ba isotopes is simulated for both transitions (553 nm and 413 nm) and for different angles between atomic beam and laser beam (90°, 85° and 80°). The simulations show, that under ideal conditions (when the atomic beam and ionization laser beam are orthogonal) both transitions perform similarly. However, the 553 nm transition exhibits greater robustness against Doppler shifts as the angle deviates from 90°. At an angle of 80° between the atomic beam and the laser beam, the maximum probability of generating 138Ba+ is 99 % using 553 nm, while the maximum probability of generating the isotope using 413 nm does not exceed 94 %. In the third part of this thesis, we focus on state preparation of Ba+ ions in the 6P1/2 state. A heralding state preparation scheme that exploits the spontaneous emission of a 389 nm photon during the decay of the excited state 6D3/2 is introduced. The detection of a photon at this wavelength projects the ion into the desired state 6P1/2 in a deterministic fashion. A simulation of this scheme shows that the preparation probability may exceed 78 %, and the heralding process ensures state preparation with 100 % fidelity, if a photon at a wavelength of 389 nm is detected. The state preparation method will be adopted in near-future experiments that are provided as an outlook at the end of this thesis.
We report on the isotope-selective manipulation of Ca + using the laser-heating and laser-cooling techniques in a linear Paul trap. Only 40 Ca + was selectively laser-heated using the optical isotope shift and eliminated from the trap while keeping the target isotope in the trap. The elimination process of the dominant isotope 40 Ca + was investigated and 42, 43, 44, 48 Ca + in the natural isotope mixture of Ca + generated by laser ablation were successfully observed by means of applying the appropriate dc voltage on the end-cap electrodes without changing the laser frequencies, the laser powers and the duration of the laser irradiation. This simplified method enables us to efficiently laser-cool the rare isotopes.