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State-changing collisions between Xenon Rydberg atoms and neutral targets

Higgs, Charles

Published Jan 1, 1982• 0 citations
OpenAlex

Abstract

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.

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Collisions of Rydberg atoms with neutral targets

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International Reviews in Physical Chemistry•Apr 3, 2018•5 citations
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.
Thermal collisions between Xe(nf) Rydberg atoms and HF molecules have been investigated. The highly excited collision products were detected using selective field ionisation (SFI). Both n-changing and l-changing collisions were identified and the absolute rate constants for these processes, and for collisional ionisation, have been measured for n=26, 27. In addition, the first evidence of molecular rotational excitation through the transfer of energy of electronic excitation from a Rydberg atom is presented.
In thermal collisions between Xe(nf) Rydberg atoms and NH(,3) collisional depopulation of the nf state occurs through at least three distinct mechanisms: n-changing collisions, l-changing collisions, and ionizing collisions. Using selective field ionization, the total collisional depopulation rate constants k(,d) are measured for laser-excited Xe(nf) atoms in the n range of 22 to 39. The magnitudes of k(,d) are large, corresponding to reaction cross sections comparable to the geometric size of the Xe(nf) atom at n = 22. In the n range of 25 to 40, Xe('+) ion production provides an absolute measure of the rate constants for collisional ionization. Approximate rate constants for n-and l-changing collisions are also presented for the 31f state. In these experiments, one finds that the state-changing collision rate constants are fairly independent of n and are determined largely by the l-changing collisions. The collisional ionization rate constants measured are smaller than the state-changing rate constants and increase with increasing n, ranging between 0.2 and 4.6 x 10('-7) cm('3)/sec for n between 25 and 40. The present results are compared to those of recent theoretical calculations.
The title process with simultaneous rotational deexcitation of molecules was investigated theoretically by using the semiquantal approximation. The dipole Born and dipole Glauber differential cross sections were employed for the electron-molecule rotational deexcitation process. Numerical applications were made to the following systems: Xe+CO, HCl, HF, and LiF. A comparative study of the two approximations was carried out concerning the dependences of the cross sections on the following various quantities: n (principal quantum number), J (initial rotational quantum number), \ensuremath{\Delta}J (rotational quantum number change), D (dipole moment), V (relative collision velocity). As the molecular dipole moment becomes larger, there appears a prominent difference in the n dependence of the cross section. The Glauber approximation brings about a decrease in the cross section and yields a sawlike n dependence in contrast to a steplike n dependence in the case of the Born approximation. In the collisions involving lowly excited Rydberg atoms, ionization with simultaneous dipole-forbidden transition of a molecule becomes dominant compared to the ionization with simultaneous dipole-allowed transition. The cross section was found to be inversely proportional to the relative collision velocity; thus the ionization rate becomes independent of temperature. A comparison was also made between the experiment for the ionization rate at 300 K for Xe(27f)+HF and Xe(31f)+HCl.
In collisions with NH3{\mathrm{H}}_{3}H3​ molecules it is observed that Xe(nf)\mathrm{Xe}(\mathrm{nf})Xe(nf) Rydberg atoms are selectively excited to discrete, more highly excited states. These states are identified by the technique of field ionization and are found to be displaced in energy from the initial Rydberg states by amounts equal to the rotational spacings of the NH3{\mathrm{H}}_{3}H3​ molecule. These measurements demonstrate, for the first time, the conversion of rotational energy to electronic energy in collisions.
Simple analytical formulas are given that allow the rapid estimation of cross sections for lll mixing, nnn changing, and ionization of Rydberg atoms with atomic and molecular targets. These formulas are derived by using the quasifree-electron model and the impulse approximation. The lll dependence of the cross section is accounted for only via the atomic energy. The quasielastic process of angular-momentum mixing caused by either the short- or long-range interaction between the Rydberg electron and the neutral perturber is studied and the corresponding cross sections are evaluated. The Rydberg-atom---molecule inelastic transitions (nnn changing and ionization) caused by the ${e}^{\ensuremath{-}}$-dipole or ${e}^{\ensuremath{-}}$-quadrupole interaction are investigated. It is shown that the nnn-changing reactions occur via quasiresonant internal-energy transfer between the two colliding partners. The influence of the relevant physical parameters is clearly stated for the three types of interaction (short-range, ${e}^{\ensuremath{-}}$-dipole, ${e}^{\ensuremath{-}}$-quadrupole). Comparison with more sophisticated approaches and experimental data shows that the accuracy of the formulas is about a factor of 2.
Atoms in highly excited Rydberg states possess physical characteristics quite unlike those associated with atoms in the ground or low-lying excited states. In particular, they are physically very large and are only very weakly bound. In consequence, collisions can lead to a wide variety of reaction processes many of which are unique to Rydberg species and have very large collision cross sections. In collisions with neutral targets, Rydberg atoms behave not as an atom but rather as a pair of well-separated independent scatterers, namely the core ion and the excited Rydberg electron. In the present article we discuss many of the different reactions that can occur when Rydberg atoms collide with neutral targets, focusing principally on reactions that are dominated by (binary) Rydberg electron-target interactions and include collisions with molecules that attach free low-energy electrons and with polar targets. In certain situations, however, interactions involving the Rydberg core ion are important. This is illustrated using as an example the destruction of ultralong-range Rydberg molecules excited in a cold dense gas.