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arXiv:0712.0222

2-photon ionization and necessary laser and vacuum systems for experiments with trapped strontium ions

Emil Kirilov, Seth Putterman

Published Dec 3, 2007• 0 citations
arXivHTMLPDF

Abstract

We describe a efficient way to photoionize strontium atoms in a linear radio-frequency trap. We use a 2-photon second order process to excite the autoionization resonance (4d2 + 5p2) 1D2. A doubled pulsed Ti:Saphire laser system is used at 431nm to provide 100fsec pulses at 82Mhz. The fabrication of the laser systems for addressing the Sr+ transitions necessary for laser cooling and excitation of quantum jumps, vacuum system and ion trap structure are also described in detail. With the current setup a easy and repeatable trapping of linear ion chains is achieved at UHV pressures.

DOI
10.48550/arxiv.0712.0222

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We describe a efficient way to photoionize strontium atoms in a linear radio-frequency trap. We use a 2-photon second order process to excite the autoionization resonance (4d2 + 5p2) 1D2. A doubled pulsed Ti:Saphire laser system is used at 431nm to provide 100fsec pulses at 82Mhz. The fabrication of the laser systems for addressing the Sr+ transitions necessary for laser cooling and excitation of quantum jumps, vacuum system and ion trap structure are also described in detail. With the current setup a easy and repeatable trapping of linear ion chains is achieved at UHV pressures.
We report a demonstration of simple and effective loading of strontium ions into a linear radio frequency Paul trap using photoionization. The ionization pathway is 5s2 1S0 -- 5s5p 1P1 -- 5p2 1D2, and the 5p2 1D2 final state is auto-ionizing. Both transitions are driven using diode lasers: a grating-stabilized 922 nm diode doubled in a single pass through potassium niobate to 461 nm and a bare diode at 405 nm. Using this technique, we have reduced the background pressure during the ion loading process by a factor of 2 compared to the conventional technique of electron bombardment. Initial ion temperatures are low enough that the ions immediately form crystals. It is also possible to observe the trapping region with a CCD camera during ion creation, allowing specific ion number loading with high probability.
We report on the single and double multiphoton ionization of ground state Sr atoms observed in an atomic beam experiment with laser pulses of ∼5 ns duration, maximum intensity ∼4 × 10 11 W cm −2 and within the 710–740 nm wavelength range. The Sr + spectrum consists of two strong lines originating from three-photon resonant four-photon ionization of bound states, a number of weak autoionizing resonances and a broad line due to four-photon excitation of the doubly excited 5p 2 1 S 0 state. The latter, along with a strong, broad and structured spectral feature, is also evident in the wavelength dependence of the doubly charged Sr 2+ ion. A weakly evident but reproducible inflection point ('knee' structure) appears in the intensity dependence of the Sr 2+ yield at the location of the 5p 2 1 S 0 resonance. A complementary fluorescence experiment revealed the accumulation of population in the 5p 1/2 , 3/2 , 6s 1/2 and 5d 3/2 , 5/2 excited Sr + states during the laser pulse. All fluorescence signals depend on laser wavelength in a manner similar to the recorded Sr + spectrum. The population accumulation in the 5p 1/2 , 3/2 ionic states unambiguously proves the absorption of two photons above the first 5s 1/2 atomic threshold while that of the 5d 3/2 , 5/2 and 6s 1/2 ones suggest the absorption of at least two more. Since under our laser pulse duration and intensity the absorption of such a number of photons in an unstructured continuum is highly improbable, it may be concluded that the process is mediated by dense manifolds of near- resonant doubly excited states, their role in the dynamics of laser–atom interaction under our conditions being far more crucial than in studies conducted using intense ultrashort pulses.
Atomic cadmium ions are loaded into radiofrequency ion traps by photoionization of atoms in a cadmium vapor with ultrafast laser pulses. The photoionization is driven through an intermediate atomic resonance with a frequency-quadrupled mode-locked Ti:sapphire laser that produces pulses of either $100\text{\ensuremath{-}}\mathrm{fs}$ or $1\text{\ensuremath{-}}\mathrm{ps}$ duration at a central wavelength of 229nm229\phantom{\rule{0.3em}{0ex}}\mathrm{nm}229nm. The large bandwidth of the pulses photoionizes all velocity classes of the Cd vapor, resulting in a high loading efficiency compared to previous ion trap loading techniques. Measured loading rates are compared with a simple theoretical model, and we conclude that this technique can potentially ionize every atom traversing the laser beam within the trapping volume. This may allow the operation of ion traps with lower levels of background pressures and less trap electrode surface contamination. The technique and laser system reported here should be applicable to loading most laser-cooled ion species.
The development of an all-solid-state systems of lasers is described for the cooling and probing of strontium ions in a radio-frequency (rf) trap. The Sr+ ions created within the rf trap are laser cooled by repeated cycling on the 422 nm 2S1/2 - 2P1/2 resonance transition. The 422 nm light was generated from a single mode 70 mW 844 nm diode laser, whose output was frequency doubled to 422 nm in a KNbO3 crystal inside a resonant enhancement cavity. Decays from the Sr+ upper resonance level into the 2D3/2 metastable state remove ions from the cooling cycle. This loss was prevented by driving the 1092 nm 2D3/2 - 2P1/2 transition using a Nd3+-doped fiber laser, diode-pumped at 826 nm. The 2S1/2 - 2D5/2 optical 'clock' transition at 674 nm has a natural linewidth of 0.4 Hz and may be probed with an AlGaInP laser diode. The laser diodes at 844 nm and 674 nm are both collimated using a piezo-mounted GRIN rod which also provides longitudinal mode selection. The spectral output is optically narrowed using resonant optical feedback.
We demonstrate a linear radio-frequency trap for confining strontium ions that is simply constructed nearly entirely with commercial off-the-shelf components. The electrodes of this trap are spaced to allow tight radial confinement, and segmented to give tight axial confinement with minimal distortion of the radio-frequency field. The resulting secular frequencies of the trap are 1 MHz in the radial direction and 100 kHz in the axial direction, the ions can be imaged with 2–3 μm resolution, and we detect over 20 000 photons per second per ion. This article describes the construction of the vital parts of the trap system, the laser system and optics used to Doppler cool the ions and to observe quantum jumps, and the operation and behavior of the complete system.
This paper reports on trapping and laser cooling of singly ionized strontium ions in a linear Paul trap. We describe the loading technique based on two-photon absorption of femtosecond pulses at a wavelength of 431 nm and we compare this technique to electron-bombardment ionization. We perform Doppler cooling of the ions in the few-ions regime as well as in the case of large clouds. The analysis of the fluorescence spectra and direct imaging of the cloud allows us to identify the Coulomb-crystal regime. These experiments open the way to the use of a large cold trapped-ion cloud as a medium for quantum optics and quantum information experiments.