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IEEE Journal of Quantum Electronics

Laser highly selective ionization detector of single atoms and its applications

G. I. Bekov, Vladilen S Letokhov, V.I. Mishin

Published Sep 1, 1979• 0 citations
Publisher
DOI
10.1109/jqe.1979.1070110

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Resonance ionization spectroscopy, RIS, is a multistep photon absorption process in which the final state is the ionization continuum of an atom. The RIS process can be saturated with available pulsed lasers, so that one electron can be removed from each atom of the selected type. This method was first applied to the determination of the absolute number of He(21S2^{1}S21S) excited states produced when pulsed beams of protons interacted with helium gas. Laser schemes for RIS are classified into five basic types; with these, nearly all of the elements can be detected with commercially available lasers. A periodic table is included showing schemes applicable to all of the elements except He, Ne, F, and Ar. A compact theory of the RIS process is presented which delineates the conditions under which rate equations apply. Questions on the effects of collisional line broadening, laser coherence time, and nonresonant multiphoton ionization processes are discussed. The initial demonstration of one-atom detection of Cs is described. By using laser beams to saturate the RIS process and by using proportional counters as single-electron detectors, one-atom detection is made possible. With RIS, one-atom detection is highly selective, has the ultimate in sensitivity, and has excellent space and time resolution. Furthermore, a modification of the technique in which single electrons (or single ions) are detected with a channel electron multiplier permits single-atom detection in a vacuum. Resonance ionization spectroscopy has application to classical phenomena such as the diffusion of free atoms, the chemical reaction of free atoms with a gas, the measurement of concentration fluctuations in a dilute vapor, and a variety of other atomic fluctuation phenomena. The authors describe how RIS can be used for photophysics measurements such as far wing collisional line broadening, measurements of photoionization cross sections for excited states, and collisional redistribution among excited states. Modern applications include the detection of single atoms in individual ionization tracks, such as those created by the binary fission of a parent atom, and the extension of this technique to the detection of stable or unstable daughter atoms in time coincidence with the decay of a parent atom. These methods are beig developed for use in low-level counting to determine, for example, the flux of solar neutrinos on the earth.
In this paper, we describe the preparation and detection of ultracold atoms on a microchip with single-atom sensitivity. The detection scheme is based on multi-photon ionization of atoms and the subsequent guiding of the generated ions by ion optics to a channel electron multiplier. We resolve single atoms with a detection efficiency above 60%. The detector is suitable for real-time observations of static and dynamic processes in ultracold quantum gases. Although the ionization is destructive, sampling a small subset of the atomic distribution is sufficient for the determination of the desired information. We take full high-resolution spectra of ultracold atoms by ionizing only 5% of the atoms. Using an additional microwave near 6.8 GHz, the detection scheme becomes energy, position and state selective. This can be used for in situ determination of the energy distribution and temperature of atom clouds inside the trap and applied for future correlation measurements.
We present a compact, ionization-based detector for the state-selective and spatially resolved measurement of individual Rydberg atoms trapped in the vicinity of an atom chip. The system combines an electrostatic lens system for guiding charged particles with an array of channel electron multipliers (CEMs) capable of detecting both ions and electrons produced by ionization. Designed for quantum information applications, this device enables the detection of correlations between spatially separated Rydberg qubits. Additionally, the electrodes provide compensation for stray electric fields and control over particle trajectories. The imaging system achieves a total magnification of more than 12, with a single-axis magnification up to 200, while maintaining low aberrations. We characterize the performance of the system using a charged particle trajectory simulation software and discuss how a coincidence measurement of ions and electrons can be used to calibrate the detection efficiency. This detector enables high-fidelity measurement of multiple Rydberg atoms and is well-suited for applications in cavity-mediated quantum gates.