Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Conference on Lasers and Electro-Optics

Two-Photon Excitation of the n=3 Level in H and D Atoms

Jeffrey Bokor A, Richard R. Freeman, J. C. White, R. H. Storz

Published Jan 1, 1981• 2 citations
Publisher

Abstract

We report the first observation of two-photon excitation from the n=1 to the n=3 level in hydrogen atoms. The process was detected by both laser-induced- fluorescence from the 656 ran Balmer α transition and two-photon resonant three-photon ionization. The excitation source used was a tunable argon-fluoride excimer laser1, which was frequency shifted via stimulated Raman scattering in D2.

DOI
10.1364/cleo.1981.ths8

Related papers

Two-photon excitation of the n = 3 level in H and D atoms

Jeffrey Bokor A, Richard R. Freeman, J. C. White +1 more

Tunable coherent ultraviolet radiation has been used to excite selectively the $n=3$ level in hydrogen and deuterium atoms via two-photon absorption from the ground state. The resulting Balmer-$\ensuremath{\alpha}$ fluorescence at 656 nm was observed as well as resonant three-photon ionization. This work demonstrates several advantages over other techniques for selective detection of neutral H and D atoms, including three-dimensional spatial resolution and a remote monitoring capability afforded by the use of laser-induced-fluorescence detection.

IEEE Journal of Quantum Electronics•Dec 1, 1981•3 citations

Two-photon excitation of the n=3 level in H and D atoms

Jeffrey Bokor A, Richard R. Freeman, J. C. White +1 more

Tunable coherent ultraviolet radiation has been used to excite selectively the $n=3$ level in hydrogen and deuterium atoms via two-photon absorption from the ground state. The resulting Balmer-$\ensuremath{\alpha}$ fluorescence at 656 nm was observed as well as resonant three-photon ionization. This work demonstrates several advantages over other techniques for selective detection of neutral H and D atoms, including three-dimensional spatial resolution and a remote monitoring capability afforded by the use of laser-induced-fluorescence detection.

Physical Review A•Jul 1, 1981•124 citations

Detection of atomic hydrogen at low density by two-photon spectroscopy

Philippe Verkerk, G. Grynberg

We have observed the 1S—3S and 1S—3D Doppler-free two-photon transitions in atomic hydrogen using a powerful narrow-band tunable light source at 205 nm. The excitation is monitored by looking at the fluorescent light emitted on the Balmer α transition. By this method we have been able to detect atomic hydrogen and atomic deuterium at low density (around 107-108 at/cm3). One of the possible applications of this method is the search of superheavy hydrogen atoms. These atoms composed of a heavy proton and an electron are predicted by some supersymmetry theories.1 Because of their important mass shift, they should be easily distinguishable from hydrogen, deuterium, or tritium. Using a preliminary centrifugation, we believe that we can improve the present limit (~10−15) on the abundance of these superheavy atoms.

Annual Meeting Optical Society of America•Jan 1, 1989•0 citations

Two-photon excitation of dense sodium vapor near the n d 2D5/2, 3/2 (n=3, 4, 5) levels: Na2 1 3Σ+g→1 3Σ+u excimer emission

Stanley J. Bajic, R. N. Compton, John A. D. Stockdale +1 more

Laser excitation and ionization processes in dense (1–10 Torr) sodium vapor have been studied for laser wavelengths near the two-photon allowed nd 2D(n=3, 4, 5) and ns 2S(n=4, 5, 6) states. In particular, the 1 3Σ+g→1 3Σ+u excimer emission in Na2, predicted in 1980 by Konowalow and Julienne and observed recently by Dinev et al, was studied here in greater detail. Strong excimer emission (∼830 nm) was observed for two-photon pumping to both sides of the unresolved 4D states, and weak excimer emission was seen when pumping near the 5D levels. The excimer emission exhibits a complicated pump laser profile with a pronounced ‘‘dip’’ at the 4d 2D two-photon resonance. Similarly, [2+1] photon ionization via the 3d 2D and 4d 2D states shows a dramatic decrease as the sodium density increases. These results can be attributed either to depleted 3d 2D or 4d 2D population due to stimulated electronic Raman scattering (SERS) or to the interference effects recently reported by Malcuit et al. and Krasnikov et al. and treated theoretically by Manykin and Afanas’ev and by Agarwal. It is argued that both mechanisms are operative. Strong ionization and SERS signals were observed at the hybrid resonances corresponding to 3p 2P3/2, 1/2 →4d 2D transitions; however, no excimer lasing at 830 nm was detected. No excimer emission was detected upon two-photon pumping near or at the 3d 2D or ns 2S(n=4, 5, 6) states. Based on these and other observations, the 1 3Σ+g→1 3Σ+u excimer emission is attributed to a molecular Raman process involving stimulated emission or six-wave mixing via a pathway of the type 1 3Σ+u→2hν 3Δu→ j 3Πg→(k 3Πu, l 3Σ +u)→1 3Σ+g→1 3Σ +u .

The Journal of Chemical Physics•Dec 15, 1988•12 citations

Two-photon excitation of dense sodium vapor near the nd /sup 2/D/sub 5/2,//sub //sub 3/2/ (n = 3, 4, 5) levels: Na/sub 2/ 1 /sup 3//Sigma//sup +//sub g//yields/1 /sup 3//Sigma//sup +//sub u/ excimer emission

Stanley J. Bajic, R. N. Compton, John A. D. Stockdale +1 more

Laser excitation and ionization processes in dense (1--10 Torr) sodium vapor have been studied for laser wavelengths near the two-photon allowed nd /sup 2/D(n = 3, 4, 5) and ns /sup 2/S(n = 4, 5, 6) states. In particular, the 1 /sup 3//Sigma//sup +//sub g//yields/1 /sup 3//Sigma//sup +//sub u/ excimer emission in Na/sub 2/, predicted in 1980 by Konowalow and Julienne and observed recently by Dinev et al, was studied here in greater detail. Strong excimer emission (/similar to/30 nm) was observed for two-photon pumping to both sides of the unresolved 4D states, and weak excimer emission was seen when pumping near the 5D levels. The excimer emission exhibits a complicated pump laser profile with a pronounced ''dip'' at the 4d /sup 2/D two-photon resonance. Similarly, (2+1) photon ionization via the 3d /sup 2/D and 4d /sup 2/D states shows a dramatic decrease as the sodium density increases. These results can be attributed either to depleted 3d /sup 2/D or 4d /sup 2/D population due to stimulated electronic Raman scattering (SERS) or to the interference effects recently reported by Malcuit et al. and Krasnikov et al. and treated theoretically by Manykin and Afanas'ev and by Agarwal. It is argued thatmore » both mechanisms are operative.« less

•Dec 15, 1988•0 citations

Two-photon Excitation of Argon

Michael Stuart Pindzola

Multiphoton excitation is describable in terms of rate equations1,2 when the generalized n-photon Rabi frequency and the excited-state photo-ionization rate are much less than the laser bandwidth. This is generally the case when powerful excimer lasers are used to excite atomic levels in rare gases. The two photon excitation rate may be written as where ω1 and ω2 are the frequencies of lasers 1 and 2 respectively, I1 and I2 are the laser intensities, G(ω1, ω2) is the bandwidth-dependent line-shape function and α is the two-photon excitation parameter defined by Eq. (1).

Topical Meeting on Laser Techniques in the Extreme Ultraviolet•Jan 1, 1982•0 citations
We report the first observation of two-photon excitation from the n=1 to the n=3 level in hydrogen atoms. The process was detected by both laser-induced- fluorescence from the 656 ran Balmer α transition and two-photon resonant three-photon ionization. The excitation source used was a tunable argon-fluoride excimer laser1, which was frequency shifted via stimulated Raman scattering in D2.
Tunable coherent ultraviolet radiation has been used to excite selectively the n=3n=3n=3 level in hydrogen and deuterium atoms via two-photon absorption from the ground state. The resulting Balmer-$\ensuremath{\alpha}$ fluorescence at 656 nm was observed as well as resonant three-photon ionization. This work demonstrates several advantages over other techniques for selective detection of neutral H and D atoms, including three-dimensional spatial resolution and a remote monitoring capability afforded by the use of laser-induced-fluorescence detection.
Tunable coherent ultraviolet radiation has been used to excite selectively the n=3n=3n=3 level in hydrogen and deuterium atoms via two-photon absorption from the ground state. The resulting Balmer-$\ensuremath{\alpha}$ fluorescence at 656 nm was observed as well as resonant three-photon ionization. This work demonstrates several advantages over other techniques for selective detection of neutral H and D atoms, including three-dimensional spatial resolution and a remote monitoring capability afforded by the use of laser-induced-fluorescence detection.
We have observed the 1S—3S and 1S—3D Doppler-free two-photon transitions in atomic hydrogen using a powerful narrow-band tunable light source at 205 nm. The excitation is monitored by looking at the fluorescent light emitted on the Balmer α transition. By this method we have been able to detect atomic hydrogen and atomic deuterium at low density (around 107-108 at/cm3). One of the possible applications of this method is the search of superheavy hydrogen atoms. These atoms composed of a heavy proton and an electron are predicted by some supersymmetry theories.1 Because of their important mass shift, they should be easily distinguishable from hydrogen, deuterium, or tritium. Using a preliminary centrifugation, we believe that we can improve the present limit (~10−15) on the abundance of these superheavy atoms.
Laser excitation and ionization processes in dense (1–10 Torr) sodium vapor have been studied for laser wavelengths near the two-photon allowed nd 2D(n=3, 4, 5) and ns 2S(n=4, 5, 6) states. In particular, the 1 3Σ+g→1 3Σ+u excimer emission in Na2, predicted in 1980 by Konowalow and Julienne and observed recently by Dinev et al, was studied here in greater detail. Strong excimer emission (∼830 nm) was observed for two-photon pumping to both sides of the unresolved 4D states, and weak excimer emission was seen when pumping near the 5D levels. The excimer emission exhibits a complicated pump laser profile with a pronounced ‘‘dip’’ at the 4d 2D two-photon resonance. Similarly, [2+1] photon ionization via the 3d 2D and 4d 2D states shows a dramatic decrease as the sodium density increases. These results can be attributed either to depleted 3d 2D or 4d 2D population due to stimulated electronic Raman scattering (SERS) or to the interference effects recently reported by Malcuit et al. and Krasnikov et al. and treated theoretically by Manykin and Afanas’ev and by Agarwal. It is argued that both mechanisms are operative. Strong ionization and SERS signals were observed at the hybrid resonances corresponding to 3p 2P3/2, 1/2 →4d 2D transitions; however, no excimer lasing at 830 nm was detected. No excimer emission was detected upon two-photon pumping near or at the 3d 2D or ns 2S(n=4, 5, 6) states. Based on these and other observations, the 1 3Σ+g→1 3Σ+u excimer emission is attributed to a molecular Raman process involving stimulated emission or six-wave mixing via a pathway of the type 1 3Σ+u→2hν 3Δu→ j 3Πg→(k 3Πu, l 3Σ +u)→1 3Σ+g→1 3Σ +u .
Laser excitation and ionization processes in dense (1--10 Torr) sodium vapor have been studied for laser wavelengths near the two-photon allowed nd /sup 2/D(n = 3, 4, 5) and ns /sup 2/S(n = 4, 5, 6) states. In particular, the 1 /sup 3//Sigma//sup +//sub g//yields/1 /sup 3//Sigma//sup +//sub u/ excimer emission in Na/sub 2/, predicted in 1980 by Konowalow and Julienne and observed recently by Dinev et al, was studied here in greater detail. Strong excimer emission (/similar to/30 nm) was observed for two-photon pumping to both sides of the unresolved 4D states, and weak excimer emission was seen when pumping near the 5D levels. The excimer emission exhibits a complicated pump laser profile with a pronounced ''dip'' at the 4d /sup 2/D two-photon resonance. Similarly, (2+1) photon ionization via the 3d /sup 2/D and 4d /sup 2/D states shows a dramatic decrease as the sodium density increases. These results can be attributed either to depleted 3d /sup 2/D or 4d /sup 2/D population due to stimulated electronic Raman scattering (SERS) or to the interference effects recently reported by Malcuit et al. and Krasnikov et al. and treated theoretically by Manykin and Afanas'ev and by Agarwal. It is argued thatmore » both mechanisms are operative.« less
Multiphoton excitation is describable in terms of rate equations1,2 when the generalized n-photon Rabi frequency and the excited-state photo-ionization rate are much less than the laser bandwidth. This is generally the case when powerful excimer lasers are used to excite atomic levels in rare gases. The two photon excitation rate may be written as where ω1 and ω2 are the frequencies of lasers 1 and 2 respectively, I1 and I2 are the laser intensities, G(ω1, ω2) is the bandwidth-dependent line-shape function and α is the two-photon excitation parameter defined by Eq. (1).