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The Journal of Chemical Physics

Effects of thermal-energy atomic and molecular collisions on lithium high-Rydberg quantum-state distributions

Carl A. Kocher, C.L. Shepard

Published Jan 1, 1981• 5 citations
Publisher

Abstract

The distribution of principal quantum numbers for high-Rydberg states of lithium, produced in a thermal atomic beam by electron impact excitation, has been determined after passage of the beam through gaseous targets. Target densities were selected for an approximately tenfold reduction of the on-axis flux of Rydberg atoms. The state distribution, determined by electric field ionization, is markedly affected by a target of rapidly rotating polar molecules having rotational energy level separations comparable to the binding energy of the Rydberg valence electron. However, the distribution is not appreciably influenced by rare-gas or slowly rotating polar molecular targets, for which the Rydberg beam spreads as a result of momentum transfer.

DOI
10.1063/1.440844

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Collisional Phenomena Between Electrons and High Rydberg Atoms.

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Highly excited (Rydberg) atoms are produced and can exist for significant periods of time in various plasma environments. It is necessary to know cross sections for the various collision processes involving these atoms if a complete understanding of the physics of these environments is to be attained.\nThe experimental investigation of collisional phenomena between high Rydberg sodium atoms and electrons is described in this thesis. A fraction of the atoms in a ground state sodium beam is optically excited (using lasers) to well-defined, high Rydberg states (principal quantum numbers chosen around 40). Subsequent to their production the Rydberg atoms are allowed to interact with 25 eV electrons for a specified time interval following which the collision products are detected. The electrons are produced in a beam which is crossed at right angles with the sodium beam. Important collision processes are (1) electron impact ionization of the Rydberg atom, and (2) electron-Rydberg atom interactions in which the quantum state of the atom is changed (state changing collisions).\nResults are presented for an observed state changing process which is identified as angular momentum state changing only (no change in the value of the principal quantum number). Cross sections for this process are measured to be 10('-10) to 10('-9) cm('2). Problems encountered during the work which prevented the measurement of electron impact ionization cross sections are discussed. In the course of the work two other topics required study: (1) the process of electric field ionization of Rydberg atoms (used to detect the atoms), and (2) the effects of background (300 K) radiation (from the chamber walls, for example) on Rydberg atoms. Results of these studies are also presented.

•Mar 1, 1980•0 citations
The distribution of principal quantum numbers for high-Rydberg states of lithium, produced in a thermal atomic beam by electron impact excitation, has been determined after passage of the beam through gaseous targets. Target densities were selected for an approximately tenfold reduction of the on-axis flux of Rydberg atoms. The state distribution, determined by electric field ionization, is markedly affected by a target of rapidly rotating polar molecules having rotational energy level separations comparable to the binding energy of the Rydberg valence electron. However, the distribution is not appreciably influenced by rare-gas or slowly rotating polar molecular targets, for which the Rydberg beam spreads as a result of momentum transfer.
Lithium atoms in high Rydberg states, excited in an atomic beam by pulsed electron impact, are passed through a target gas and detected following electric-field state selection. Cross sections obtained from time-of-flight spectra are virtually independent of the principal quantum number and in numerical agreement with calculations for deflection of the core ion alone. This deflection has also been observed directly. These results suggest a new method for very-low-energy ion-atom scattering experiments.
Thermal collisions between laser excited Xe(nf) Rydberg atoms and a variety of neutral atomic and molecular targets have been investigated. In Xe(nf)-HF collisions, n-changing, 4-changing and collisional ionization were observed. For n = 26 and 27, absolute collisional cross sections for these processes have been determined using time-resolved selective field ionization. In addition, the first evidence of molecular rotational excitation through the transfer of energy of electronic excitation from a Rydberg atom is presented. In Xe(nf) - Xe, Kr, Ar, CO2, CO and N2 collisions the dominant mechanism was observed to be 4-changing: no evidence of n-changing or collisional ionization was apparent. Absolute collisional cross sections have been determined for a range of n between 24 and 37. Comparison of these cross sections with those obtained using a theoretical model in which effects due to the Rydberg core are ignored appears to lead to satisfactory results only for Xe, Kr and CO2, whereas when core effects are included satisfactory agreement between experiment and theory is found in all cases.
Using state-selective field ionization, the state distributions of Rydberg atoms in cold Rydberg gases are measured for various initially excited Rydberg levels, populations, and evolution times. We provide direct experimental evidence for lll-changing collisions that we previously observed indirectly [S. K. Dutta, D. Feldbaum, A. Walz-Flannigan, J. R. Guest, and G. Raithel, Phys. Rev. Lett. 86, 3993 (2001)]. We also observe nnn-mixing and find that its effects are largely in agreement with recent theoretical work on nnn-changing collisions between electrons and Rydberg atoms, thus enabling an estimation of the electron temperature. Unexpectedly large populations of atoms are found in states with principal quantum numbers much lower than that of the initially excited atoms. We explain this observation by collisions between high-lll Rydberg atoms, which are highly polar and can collide due to static electric-dipole forces between them.
Potassium atoms in selected high-lying np Rydberg states (80 {<=} n {<=} 400) are being used as a tool to examine electron-polar molecule collisions at ultra-low energies ({approximately}80 {mu}eV - 1 meV). This energy regime has not been investigated previously and is of interest because the corresponding electron de Broglie wavelength is large, {approximately}1300 - 330 {Angstrom}, and because the collision time is comparable to the period of molecular rotation. A variety of target molecules has been studied, including simple rotors such as HF, and more complex species such as NH{sub 3}, CH{sub 3}I, CH{sub 2}Br{sub 2} and C{sub 6}H{sub 5}NO{sub 2}. These targets encompass a range of dipole moments and rotational behavior, but analysis of the data shows that in each case the cross section {sigma}({epsilon}) for rotationally-inelastic electron-polar molecule scattering varies approximately as 1/{epsilon} where {epsilon} is the electron energy. Such threshold behavior is not predicted by the Born approximation and possible reasons for this discrepancy will be discussed. In the case of NH{sub 3}, the data show that near-resonant energy transfer associated with transitions between different inversion levels is an important process leading to collisional state changing.
Thermal collisions between potassium Rydberg atoms with intermediate values of quantum number n and target molecules that capture free low-energy electrons are investigated. The velocity, binding energy, and angular distributions of heavy-Rydberg ion-pair states formed through such collisions are measured. The experimental data are analyzed with the aid of semiclassical Monte Carlo simulations to investigate the dynamics of electron attachment to a variety of target species. Multiple reaction channels involving short- and long-lived intermediates are seen for electron capture by 1,1,1-C2Cl3F3 and CBrCl3 (where dissociation of CBrCl3 intermediates involves production of Br- and Cl- ions). Electron attachment to BrCN produces long-lived BrCN-* intermediates whose dissociation results in the creation of rotationally-hot CN- anions. Electron capture by Fe(CO)5 leads to formation of Fe(CO)5-* intermediates which can fragment producing Fe(CO)4- anions, either directly or after partial redistribution of the excess energy within the intermediate has occurred. Electron transfer in Rydberg atom collisions with C2Cl4 provide no evidence of formation of long-lived C2Cl4 ions, only Cl- ions are seen. Moreover, strong Rydberg atom scattering is observed following collisions of K(12p) Rydberg states with CH3NO2. This finding is consistent with a theory which predicts that collisions between Rydberg atoms with intermediate values of n and polar molecules can lead to strong resonant quenching of Rydberg states, i.e., n and l changing, through formation of short-lived K+...CH3NO2- ion-pair states. Finally, the improvements in sensitivity to electron capture reaction dynamics that might be achieved using different Rydberg species and a crossed molecular beam are examined. Simulations are performed to demonstrate that the use of a hyperthermal helium Rydberg atomic beam and a crossed beam of target molecules such as CCl4, BrCN and CF3I can provide new insights into dissociative electron attachment reactions. The calculations show that not only can much detailed information on translational energy release distributions and intermediate lifetimes be obtained, but also on the electron radial probability density distributions in the Rydberg atoms themselves.
Highly excited (Rydberg) atoms are produced and can exist for significant periods of time in various plasma environments. It is necessary to know cross sections for the various collision processes involving these atoms if a complete understanding of the physics of these environments is to be attained.\nThe experimental investigation of collisional phenomena between high Rydberg sodium atoms and electrons is described in this thesis. A fraction of the atoms in a ground state sodium beam is optically excited (using lasers) to well-defined, high Rydberg states (principal quantum numbers chosen around 40). Subsequent to their production the Rydberg atoms are allowed to interact with 25 eV electrons for a specified time interval following which the collision products are detected. The electrons are produced in a beam which is crossed at right angles with the sodium beam. Important collision processes are (1) electron impact ionization of the Rydberg atom, and (2) electron-Rydberg atom interactions in which the quantum state of the atom is changed (state changing collisions).\nResults are presented for an observed state changing process which is identified as angular momentum state changing only (no change in the value of the principal quantum number). Cross sections for this process are measured to be 10('-10) to 10('-9) cm('2). Problems encountered during the work which prevented the measurement of electron impact ionization cross sections are discussed. In the course of the work two other topics required study: (1) the process of electric field ionization of Rydberg atoms (used to detect the atoms), and (2) the effects of background (300 K) radiation (from the chamber walls, for example) on Rydberg atoms. Results of these studies are also presented.