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arXiv:2402.17981 · Journal of Physics D Applied Physics

Dynamic laser ablation loading of a linear Paul trap

Lin Li, Zi Li, Xia Hua, Xin Tong

Published Apr 29, 2024• 7 citations
arXivHTMLPDF

Abstract

Abstract We present a detailed method for accumulating Ca+ ions controllably in a linear Paul trap. The ions are generated by pulsed laser ablation and dynamically loaded into the ion trap by switching the trapping potential on and off. The loaded ions are precooled by buffer gas and then laser-cooled to form Coulomb crystals for verifying quantity. The number of ions is controlled by manipulating the trapping potential of the ion trap, partial pressure of buffer gas and turn-on time of the entrance end cap voltage. With single-pulse laser ablation, the number of trapped ions ranges from tens to ten thousand. The kinetic energy of loaded ions can be selected via the optimal turn-on time of the entrance end cap. Using multiple-pulse laser ablation, the number is further increased and reaches about 4 × 10 4 . The dynamic loading method has wide application for accumulating low-yielding ions via laser ablation in the ion trap.

DOI
10.1088/1361-6463/ad449f

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Abstract We present a detailed method for accumulating Ca+ ions controllably in a linear Paul trap. The ions are generated by pulsed laser ablation and dynamically loaded into the ion trap by switching the trapping potential on and off. The loaded ions are precooled by buffer gas and then laser-cooled to form Coulomb crystals for verifying quantity. The number of ions is controlled by manipulating the trapping potential of the ion trap, partial pressure of buffer gas and turn-on time of the entrance end cap voltage. With single-pulse laser ablation, the number of trapped ions ranges from tens to ten thousand. The kinetic energy of loaded ions can be selected via the optimal turn-on time of the entrance end cap. Using multiple-pulse laser ablation, the number is further increased and reaches about 4 × 10 4 . The dynamic loading method has wide application for accumulating low-yielding ions via laser ablation in the ion trap.
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.
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.
Coulomb crystals, containing up to a few hundred ions of which more than 50% were cooled sympathetically by the Coulomb interaction with laser cooled Mg+ ions, have been produced in a linear Paul trap. By controlling the balance of the radiation pressure from the two cooling lasers, the Coulomb crystals could be segregated according to ion species. Previous studies of ion crystals and molecular dynamics simulations suggest that the temperature may be around 10 mK or lower. The obtained results indicate that a wide range of atomic and molecular ions, which due to their internal structures are not amenable to direct laser cooling, can be effectively cooled and localized (crystallized) in linear Paul traps. For high resolution spectroscopy of such ions this may turn out to be very useful.
We have investigated the efficiency of ion trapping in a linear Paul trap. First, we measured the dependence of trapping efficiency on dc and rf voltages using a channel electron multiplier for the direct detection of the electric current of the trapped ions. The most efficient dc and rf voltages were 5.0 and 175 V, respectively. Second, we calculated the trapping efficiency using a simulation code and compared it with the experimental results. We determined that the efficiency of ion trapping decreased monotonically with increasing dc voltage and had an optimum rf voltage. From the numerical calculation, the dependences of trapping efficiency on dc and rf voltages and the initial kinetic energy of ions was derived and the optimum dc and rf voltages and the initial kinetic energy of ions were found to be 0, 210 V, and 1 eV, respectively.
Trapped atomic ions find wide applications ranging from precision measurement to quantum information science and quantum computing. Beryllium ions are widely used due to the light mass and convenient atomic structure of beryllium; however, conventional ion loading from thermal ovens exerts undesirable gas loads for a prolonged duration. Here, we demonstrate a method to rapidly produce pure linear chains of beryllium ions with pulsed laser ablation, serving as a starting point for large-scale quantum information processing. Our method is fast compared to thermal ovens, reduces the gas load to only 10−12 Torr (10−10 Pa) level, yields a short recovery time of a few seconds, and also eliminates the need for a deep ultraviolet laser for photoionization. We also study the loading dynamics, which show non-Poissonian statistics in the presence of sympathetic cooling. In addition, we apply feedback control to obtain defect-free ion chains with desirable lengths.