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Lund reports on atomic physics

Time Resolved Laser Spectroscopy of Rydberg States in Group IIIA and IIIA Elements

Goran B Jönsson

Published Jan 1, 1984• 0 citations
OpenAlex

Abstract

In this work radiative properties of neutral elements with one or two electrons outside closed subshells have been investigated. Using laser techniques in connection with atomic beams selective excitation of Rydberg states was performed. Most of the studied states were populated with two-step excitation. Some states were reached directly from the ground state or from a metastable state and occasionally two-photon absorption was used. The excitation sometimes involved the use of frequency-doubling and Raman- shifting techniques. By time-resolved detection of the decay light from an excited state, primarily information on the radiative lifetime is obtained. With two different experimental arrangements radiative lifetimes in several Rydberg states have been determined. Using the quantum-beat technique time-resolved detection also provides information on energy splittings. This technique was used to measure hyperfine-structure splittings.To obtain information about hyperfine-structure constants and isotope shifts high- resolution spectroscopy on a collimated atomic beam was also employed. The behaviour of highly excited alkali atoms is mostly hydrogen- like and well predicted by theory. Group III A elements have one electron outside a closed subshell and are expected to behave like alkali atoms. The situation is however complicated by the presence of doubly excited states. Configuration interaction can then cause a partial mixing between singly and doubly excited states. In the alkaline-earth atoms (group II A elements), having two electrons outside closed shells, the situation is similar. In a Rydberg series of one excited electron the admixture of doubly excited states can cause large deviations from hydrogenic behaviour. Another complication in the alkaline-earth atoms is the mixture of singlet- and triplet states. - 4 - The presented results from measurements made on Na, Mg, Ca, Sr, Ba, Al, Ga and In will primarily serve as a basis for tests of modern atomic-physics models. Some of the lifetime values are also of astrophysical interest. Keywords: Laser spectroscopy, Rydberg states, time resolved, high resolution, two-step excitation, metastable state, two-photon absorption, frequency doubling, Raman shifting, radiative lifetime, quantum beat, hyperfine structure, isotope shift, Stark shift, alkali atoms, group III A elements, alkaline-earth atoms, configuration interaction, singlet-triplet mixing.

Related papers

High-resolution Rydberg-state spectroscopy of stable alkaline-earth elements

R. Beigang

High-resolution Rydberg-state spectroscopy was applied to investigate high-lying Rydberg states of the alkaline-earth elements Mg, Ca, Sr, and Ba up to principal quantum numbers n > 200. In this energy range interactions dominate that are negligible at low n. It is shown that the hyperfine interaction can be used as a sensitive probe for configuration interactions, singlet–triplet mixing, and hyperfine-induced n mixing.

Journal of the Optical Society of America B•Dec 1, 1988•6 citations

Recent advances in Rydberg physics using alkaline-earth atoms

F. B. Dunning, T. C. Killian, S. Yoshida +1 more

Abstract In this brief review, the opportunities that the alkaline-earth elements offer for studying new aspects of Rydberg physics are discussed. For example, the bosonic alkaline-earth isotopes have zero nuclear spin which eliminates many of the complexities present in alkali Rydberg atoms, permitting simpler and more direct comparison between theory and experiment. The presence of two valence electrons allows the production of singlet and triplet Rydberg states that can exhibit a variety of attractive or repulsive interactions. The availability of weak intercombination lines is advantageous for laser cooling and for applications such as Rydberg dressing. Excitation of one electron to a Rydberg state leaves behind an optically active core ion allowing, for high- L states, the optical imaging of Rydberg atoms and their (spatial) manipulation using light scattering. The second valence electron offers the possibility of engineering long-lived doubly excited states such as planetary atoms. Recent advances in both theory and experiment are highlighted together with a number of possible directions for the future.

Journal of Physics B Atomic Molecular and Optical Physics•May 9, 2016•49 citations

Two-photon spectra of Rydberg states of alkaline-earth atoms (strontium and barium)

G. Philip

The even-parity spectra of strontium and barium are very complex due to strong perturbation by several doubly excited configurations and this also increases discrepancies between theory and experiment in accurate level assignment and energy level and atomic structure data, particularly for the spectra of highly excited atoms and their behaviour in external fields and collisional processes which are of fundamental importance in the emerging applications in physics of cold atoms, quantum computing, precision atomic clocks and in the crossed-field problem. This thesis presents results from an experimental study to improve and extend the previously published observations in the two-photon spectra of the high-lying Rydberg states of SrI and Bal placed under a variety of test conditions such as external fields, collisions etc. Orthogonal excitation of a novel atomic jet in a purpose-built heat-pipe setup using a Xenon Chloride excimer laser pumped tunable narrow bandwidth dye laser and high sensitivity space-charge ionization in thermionic diode with complimentary optical detection was used for measurements. Presented are the two-photon spectra covering the dye laser wavelength (air) range of 460 - 425 nm for strontium and 495 - 467 nm for barium by which the J = 0,2 even-parity Rydberg series and autoionizing resonances just above the ionization limits labeled as; (4d2+5p2) 1D2 in strontium and 5d5f2p1 in barium were observed. Original new energy level values are presented with substantial extension to the data in the literature for even-parity Rydberg series: Sr I: 5sns 1S0 (12 < n < 46), 5snd 3D2 (9 < n < 47) and 5snd 1D2 (9 < n < 82) Ba I: 6sns 1S0 (13 < n < 68), 6snd 3D2 (11 < n < 46) and 6snd 1D2 (11 < n < 88) New observation of certain anomalies including a Stark shift reversal effect and zero-field thermionic diode detection with remarkable sensitivity preserving all spectral features of Rydberg states is also presented. Controlled configuration mixing by exploiting electric field and collisions has allowed new observations for the two-photon forbidden odd-parity Rydberg series of SrI: 5s2 1S0 -> 5snp 1P1o (32 < n < 46) and 5s2 1S0 -> 5snf 1F30 (29 < n < 44) Extensive study of collision involving Rydberg atoms with neutral rare gas atoms has allowed to obtain new data for shift and broadening rates for Sr I series: 5sns 1S0 and 5snd 1,3D2 in the perturbed region which clearly exhibit Ramsauer effect. Collisional evolution of a remarkably broad resonance, labeled as 4d2 1G4, also exhibiting Ramsauer effect, is presented besides new level data for strontium 4d2 3PJ states accessed by two distinct processes- direct two-photon excitation and single-photon sequential excitation. Furthermore, the thesis presents the results of a novel experimental technique involving time-resolved gated pulsed field detection technique (GPT) employed for the first time to examine the time decay of Rydberg atoms yielding their effective lifetimes.

•Jan 1, 2008•0 citations

Direct Measurements of Excited-State Lifetimes in Group-II and Group-Iii Atoms.

Mark D. Havey

The lifetimes of a large number of excited states in the Group II and Group III atoms have been measured.Among these states are the 5s5p3Pj metastable state of Sr and the lowest 3Sj state of Mg, Ca, and Sr.Also measured were the lifetimes of the lowest 2Sa states of Al, Ga, In and Tl, and "2 the lifetimes of several andXD2 states of Ca.The ex cited states were populated by one-and two-step dye laser excitation, and the lifetimes determined by direct observa tion of the subsequent resonance or branching fluorescence.The results obtained for states in the triplet series of the Group II atoms are: t {Sr 3P ) =(21.0 ± 1.0)ysec, r{Mg 3Sl) = (9.7 ± 0.5) nsec, t(Ca 3S 1)= ( 11.7 ± 0.6) nsec,x(Sr 3Sj ) = (12.9± 0.7) nsec.ix CHAPTER X

•Jun 1, 1977•0 citations

Metastable D-state spectroscopy and laser cooling of barium

Umakanth Dammalapati

This thesis is written as a part of the TRImP programme. Rare and short-lived radioactive isotopes offer new possibilities for investigating fundamental interactions and symmetries. Radium, a radioactive alkaline earth element has been identified as a new candidate for searches for a permanent electric dipole moment in neutral atoms. The TRImP facility at KVI, Groningen, The Netherlands is being setup to produce and utilize these radioactive isotopes to study fundamental interactions and symmetries. We use atom traps for these studies. We presented the various stages for the production, separation and slowing of the short-lived radioactive isotopes of our interest at the TRImP facility. We need to expand laser cooling and trapping methods to heavy alkaline earth elements barium and radium. Stable barium is well suited as a precursor for radioactive radium, because of its similar level scheme and chemical properties. Because of the radioactivity of radium we have chosen to prepare the cooling and trapping with the homologue barium. Stable isotopes of barium were used in the present study. For spectroscopy, metastable singlet and triplet D-states were populated by optical methods rather than using the conventional method of atomic discharges. The singlet D-state is populated by driving the 1S0-1P1 transition. To populate the triplet D-states efficiently the branching ratio of the 3P1 level was exploited by optical pumping with the intercombination line using the diode lasers at 791.3 nm. Long term frequency stability of these lasers were achieved by referencing the frequency to a nearby transition in molecular iodine. We performed first direct optical spectroscopy of the 1D2-1P1(1500.4 nm), 3D1-1P1(1107.8 nm) and 3D2-1p1 (1130.6 nm) transitions respectively. The hyperfine structure of the 3D1 and 3D2 levels for the Ba-135,137 isotopes were optically resolved. In addition, isotope shifts of the 3D1-1P1 transition were measured. We report the experimental observation of coherent Raman resonances in barium. The relevant Rabi frequencies were extracted for the lambda system and estimated the transition rates, relevant for the laser cooling experiment. We have achieved the first slowing of a barium atomic beam. These results can be applied for atoms, in which a closed cooling cycle can only be found with several laser fields at different wavelengths.

•Jan 1, 2006•4 citations

A cold strontium Rydberg gas

James Millen

Cold gases of Rydberg atoms are an ideal system in which to study the novel effects of strong interatomic interactions. This thesis describes the design and construction of the world's first experiment to study Rydberg states in a cold gas of an alkaline earth metal, in this particular case strontium. We have studied a wide range of Rydberg states, and have developed a sensitive ``step-scan" spectroscopic technique that detects the spontaneous ionization of the Rydberg gas. The step-scan method is used to acquire Stark maps, and these measurements verify a single-electron model for calculating dipole matrix-elements. From the matrix-elements, interaction strengths between strontium Rydberg atoms have been calculated for the first time. The presence of two valence electrons in an alkaline earth metal, such as strontium, offers a new angle on the study of Rydberg atoms. We create doubly excited ``autoionizing" states, the first such study in a cold gas. Autoionization is used as a high yield probe of Rydberg states, and enables a study of excitation dynamics with nanosecond time-resolution. We show that autoionization can quantitatively identify and elucidate state mixing in the Rydberg gas, and probe population transfer at the very onset of ultra-cold plasma formation.

•Jan 1, 2011•6 citations
In this work radiative properties of neutral elements with one or two electrons outside closed subshells have been investigated. Using laser techniques in connection with atomic beams selective excitation of Rydberg states was performed. Most of the studied states were populated with two-step excitation. Some states were reached directly from the ground state or from a metastable state and occasionally two-photon absorption was used. The excitation sometimes involved the use of frequency-doubling and Raman- shifting techniques. By time-resolved detection of the decay light from an excited state, primarily information on the radiative lifetime is obtained. With two different experimental arrangements radiative lifetimes in several Rydberg states have been determined. Using the quantum-beat technique time-resolved detection also provides information on energy splittings. This technique was used to measure hyperfine-structure splittings.To obtain information about hyperfine-structure constants and isotope shifts high- resolution spectroscopy on a collimated atomic beam was also employed. The behaviour of highly excited alkali atoms is mostly hydrogen- like and well predicted by theory. Group III A elements have one electron outside a closed subshell and are expected to behave like alkali atoms. The situation is however complicated by the presence of doubly excited states. Configuration interaction can then cause a partial mixing between singly and doubly excited states. In the alkaline-earth atoms (group II A elements), having two electrons outside closed shells, the situation is similar. In a Rydberg series of one excited electron the admixture of doubly excited states can cause large deviations from hydrogenic behaviour. Another complication in the alkaline-earth atoms is the mixture of singlet- and triplet states. - 4 - The presented results from measurements made on Na, Mg, Ca, Sr, Ba, Al, Ga and In will primarily serve as a basis for tests of modern atomic-physics models. Some of the lifetime values are also of astrophysical interest. Keywords: Laser spectroscopy, Rydberg states, time resolved, high resolution, two-step excitation, metastable state, two-photon absorption, frequency doubling, Raman shifting, radiative lifetime, quantum beat, hyperfine structure, isotope shift, Stark shift, alkali atoms, group III A elements, alkaline-earth atoms, configuration interaction, singlet-triplet mixing.
Abstract In this brief review, the opportunities that the alkaline-earth elements offer for studying new aspects of Rydberg physics are discussed. For example, the bosonic alkaline-earth isotopes have zero nuclear spin which eliminates many of the complexities present in alkali Rydberg atoms, permitting simpler and more direct comparison between theory and experiment. The presence of two valence electrons allows the production of singlet and triplet Rydberg states that can exhibit a variety of attractive or repulsive interactions. The availability of weak intercombination lines is advantageous for laser cooling and for applications such as Rydberg dressing. Excitation of one electron to a Rydberg state leaves behind an optically active core ion allowing, for high- L states, the optical imaging of Rydberg atoms and their (spatial) manipulation using light scattering. The second valence electron offers the possibility of engineering long-lived doubly excited states such as planetary atoms. Recent advances in both theory and experiment are highlighted together with a number of possible directions for the future.
The even-parity spectra of strontium and barium are very complex due to strong perturbation by several doubly excited configurations and this also increases discrepancies between theory and experiment in accurate level assignment and energy level and atomic structure data, particularly for the spectra of highly excited atoms and their behaviour in external fields and collisional processes which are of fundamental importance in the emerging applications in physics of cold atoms, quantum computing, precision atomic clocks and in the crossed-field problem. This thesis presents results from an experimental study to improve and extend the previously published observations in the two-photon spectra of the high-lying Rydberg states of SrI and Bal placed under a variety of test conditions such as external fields, collisions etc. Orthogonal excitation of a novel atomic jet in a purpose-built heat-pipe setup using a Xenon Chloride excimer laser pumped tunable narrow bandwidth dye laser and high sensitivity space-charge ionization in thermionic diode with complimentary optical detection was used for measurements. Presented are the two-photon spectra covering the dye laser wavelength (air) range of 460 - 425 nm for strontium and 495 - 467 nm for barium by which the J = 0,2 even-parity Rydberg series and autoionizing resonances just above the ionization limits labeled as; (4d2+5p2) 1D2 in strontium and 5d5f2p1 in barium were observed. Original new energy level values are presented with substantial extension to the data in the literature for even-parity Rydberg series: Sr I: 5sns 1S0 (12 < n < 46), 5snd 3D2 (9 < n < 47) and 5snd 1D2 (9 < n < 82) Ba I: 6sns 1S0 (13 < n < 68), 6snd 3D2 (11 < n < 46) and 6snd 1D2 (11 < n < 88) New observation of certain anomalies including a Stark shift reversal effect and zero-field thermionic diode detection with remarkable sensitivity preserving all spectral features of Rydberg states is also presented. Controlled configuration mixing by exploiting electric field and collisions has allowed new observations for the two-photon forbidden odd-parity Rydberg series of SrI: 5s2 1S0 -> 5snp 1P1o (32 < n < 46) and 5s2 1S0 -> 5snf 1F30 (29 < n < 44) Extensive study of collision involving Rydberg atoms with neutral rare gas atoms has allowed to obtain new data for shift and broadening rates for Sr I series: 5sns 1S0 and 5snd 1,3D2 in the perturbed region which clearly exhibit Ramsauer effect. Collisional evolution of a remarkably broad resonance, labeled as 4d2 1G4, also exhibiting Ramsauer effect, is presented besides new level data for strontium 4d2 3PJ states accessed by two distinct processes- direct two-photon excitation and single-photon sequential excitation. Furthermore, the thesis presents the results of a novel experimental technique involving time-resolved gated pulsed field detection technique (GPT) employed for the first time to examine the time decay of Rydberg atoms yielding their effective lifetimes.
The lifetimes of a large number of excited states in the Group II and Group III atoms have been measured.Among these states are the 5s5p3Pj metastable state of Sr and the lowest 3Sj state of Mg, Ca, and Sr.Also measured were the lifetimes of the lowest 2Sa states of Al, Ga, In and Tl, and "2 the lifetimes of several andXD2 states of Ca.The ex cited states were populated by one-and two-step dye laser excitation, and the lifetimes determined by direct observa tion of the subsequent resonance or branching fluorescence.The results obtained for states in the triplet series of the Group II atoms are: t {Sr 3P ) =(21.0 ± 1.0)ysec, r{Mg 3Sl) = (9.7 ± 0.5) nsec, t(Ca 3S 1)= ( 11.7 ± 0.6) nsec,x(Sr 3Sj ) = (12.9± 0.7) nsec.ix CHAPTER X
This thesis is written as a part of the TRImP programme. Rare and short-lived radioactive isotopes offer new possibilities for investigating fundamental interactions and symmetries. Radium, a radioactive alkaline earth element has been identified as a new candidate for searches for a permanent electric dipole moment in neutral atoms. The TRImP facility at KVI, Groningen, The Netherlands is being setup to produce and utilize these radioactive isotopes to study fundamental interactions and symmetries. We use atom traps for these studies. We presented the various stages for the production, separation and slowing of the short-lived radioactive isotopes of our interest at the TRImP facility. We need to expand laser cooling and trapping methods to heavy alkaline earth elements barium and radium. Stable barium is well suited as a precursor for radioactive radium, because of its similar level scheme and chemical properties. Because of the radioactivity of radium we have chosen to prepare the cooling and trapping with the homologue barium. Stable isotopes of barium were used in the present study. For spectroscopy, metastable singlet and triplet D-states were populated by optical methods rather than using the conventional method of atomic discharges. The singlet D-state is populated by driving the 1S0-1P1 transition. To populate the triplet D-states efficiently the branching ratio of the 3P1 level was exploited by optical pumping with the intercombination line using the diode lasers at 791.3 nm. Long term frequency stability of these lasers were achieved by referencing the frequency to a nearby transition in molecular iodine. We performed first direct optical spectroscopy of the 1D2-1P1(1500.4 nm), 3D1-1P1(1107.8 nm) and 3D2-1p1 (1130.6 nm) transitions respectively. The hyperfine structure of the 3D1 and 3D2 levels for the Ba-135,137 isotopes were optically resolved. In addition, isotope shifts of the 3D1-1P1 transition were measured. We report the experimental observation of coherent Raman resonances in barium. The relevant Rabi frequencies were extracted for the lambda system and estimated the transition rates, relevant for the laser cooling experiment. We have achieved the first slowing of a barium atomic beam. These results can be applied for atoms, in which a closed cooling cycle can only be found with several laser fields at different wavelengths.
Cold gases of Rydberg atoms are an ideal system in which to study the novel effects of strong interatomic interactions. This thesis describes the design and construction of the world's first experiment to study Rydberg states in a cold gas of an alkaline earth metal, in this particular case strontium. We have studied a wide range of Rydberg states, and have developed a sensitive ``step-scan" spectroscopic technique that detects the spontaneous ionization of the Rydberg gas. The step-scan method is used to acquire Stark maps, and these measurements verify a single-electron model for calculating dipole matrix-elements. From the matrix-elements, interaction strengths between strontium Rydberg atoms have been calculated for the first time. The presence of two valence electrons in an alkaline earth metal, such as strontium, offers a new angle on the study of Rydberg atoms. We create doubly excited ``autoionizing" states, the first such study in a cold gas. Autoionization is used as a high yield probe of Rydberg states, and enables a study of excitation dynamics with nanosecond time-resolution. We show that autoionization can quantitatively identify and elucidate state mixing in the Rydberg gas, and probe population transfer at the very onset of ultra-cold plasma formation.