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Physical Review A

Photon-burst method in high-resolution laser spectroscopy

D. A. Lewis, J. F. Tonn, S. L. Kaufman, G. W. Greenlees

Published Apr 1, 1979• 24 citations

Abstract

The sensitivity of high-resolution fluorescence spectroscopy has been enhanced by the detection of bursts of photons from single atoms crossing a laser beam. A tunable cw laser beam intersected a well-collimated atomic beam at right angles, and the fluorescent light was detected by an ellipsoidal collector and a photomultiplier. The passage of an atom through the beam was identified with a burst of detected photon pulses, which could be differentiated easily from the random background. For increasing burst multiplicity the spectra show improved background suppression and also significant peak narrowing. High-resolution spectra were obtained with as few as 10 atoms/sec crossing the laser beam. Statistical predictions for the case of transit-time limited signals are calculated and compared with results obtained for the Na 5890-\AA{} and Ba 5535-\AA{} transitions.

DOI: 10.1103/physreva.19.1580

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The sensitivity of high-resolution fluorescence spectroscopy has been enhanced by the detection of bursts of photons from single atoms crossing a laser beam. A tunable cw laser beam intersected a well-collimated atomic beam at right angles, and the fluorescent light was detected by an ellipsoidal collector and a photomultiplier. The passage of an atom through the beam was identified with a burst of detected photon pulses, which could be differentiated easily from the random background. For increasing burst multiplicity the spectra show improved background suppression and also significant peak narrowing. High-resolution spectra were obtained with as few as 10 atoms/sec crossing the laser beam. Statistical predictions for the case of transit-time limited signals are calculated and compared with results obtained for the Na 5890-\AA{} and Ba 5535-\AA{} transitions.

Abstract Resonance scattering techniques are very useful for high-resolution atomic spectroscopy. The applicability of these techniques has been much extended, particularly through the rapid development of tunable-laser technology. The use of a narrow-band tunable laser, acting on a collimated atomic beam, gives a direct method enabling, for example, hyperfine structure and isotope shift studies. The intensity of lasers allows stepwise excitations to be performed, and with the two-photon absorption technique, Doppler-free measurements on thermal gases are also possible. By using pulsed lasers, time-resolved measurements yielding radiative life-times and structural information can be performed. The basic resonance scattering methods can be combined with radiofrequency and coherence techniques to yield a resolution, limited only by the uncertainty relation. Optical double resonance and level-crossing techniques, not requiring a narrow-band light source, have been extensively used. Several examples of the application of resonance scattering methods are given.

Using a digital correlator, we record the burst of photons emitted by a single atom as it passes through a resonant laser beam. A high efficiency light collection system allows us to register many counts from each atom. The transit time of the atom across the laser beam is computed from the displayed autocorrelation function. By averaging over many atoms, we determine diffusion coefficients for ground state sodium in helium, neon and argon. We have also used this technique to measure rapid flow speeds of gases.

High-peak-power ultrafast lasers are widely used in nonlinear spectroscopy, but often limit its spectral resolution because of the broad frequency bandwidth of ultrashort laser pulses. Improving the resolution by achieving spectrally narrow excitation of, or emission from, the resonant medium by means of multiphoton interferences has been the focus of many recent developments in ultrafast spectroscopy. We demonstrate an alternative approach in which high resolution is exercised by detecting narrow spectral correlations between broadband excitation and emission optical fields. All-optical correlation analysis, easily incorporated into a traditional spectroscopic setup, enables direct, robust, and simultaneous detection of multiple narrow resonances in a single measurement.

The use of highly monochromatic light permits the selective excitation of atoms in vapors if excitation and detection of the fluorescence is carried out collinearly. The atoms capable of absorbing light then form an atomic beam of well-defined velocity along the direction of the laser beam, but no velocity selection occurs perpendicular to it. The potential of the technique for Doppler-free atomic spectroscopy and for the study of excited atom collisions is demonstrated by using the Na D1 line as an example.

The use of highly monochromatic light permits the selective excitation of atoms in vapors if excitation and detection of the fluorescence is carried out collinearly. The atoms capable of absorbing light then form an atomic beam of well-defined velocity along the direction of the laser beam, but no velocity selection occurs perpendicular to it. The potential of the technique for Doppler-free atomic spectroscopy and for the study of excited atom collisions is demonstrated by using the Na D1 line as an example.