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Advances in electronics and electron physics

Rydberg Atom Collision Processes

F. B. Dunning, R. F. Stebbings

Published Jan 1, 1982• 5 citations
Publisher
DOI
10.1016/s0065-2539(08)60109-2

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In the present work very-high-n Rydberg-atoms $(n \\sim 100 - n \\sim 400)$ are used to probe electron-molecule collisions at ultra-low electron energies. Based on the essentially-free-electron model, for sufficiently high n, Rydberg atom-molecule collisions can be described in terms of a binary interaction between the target molecule and the essentially-free Rydberg electron. Since the average kinetic energy of the Rydberg electron is ultra-low $\\rm({\\sim}85\\mu eV - {\\sim}1.4meV),$ analysis of the very-high-n Rydberg-atom collision data can provide information on electron-molecule scattering at electron energies corresponding to electron temperatures of only $\\sim$1$\\sp\\circ$K, which are far below those accessible using any alternate approach.\nRate constants for destruction of very-high-n Rydberg atoms in collisions with various target molecules have been measured. This study focuses on Rydberg electron transfer to an electron-attaching molecule which results in negative ion formation via the reactions $$\\rm K({\\it np\\/}) + XY \\to K\\sp+ + (XY)\\sp{-*}\\ or\\ \\to K\\sp+ + X\\sp- + Y\\eqno(1)$$and on rotational energy transfer from polar molecules which leads to Rydberg atom ionization $$\\rm K({\\it np\\/}) + XY({\\it J\\/}) \\to K\\sp+ + {\\it e}\\sp- + XY({\\it J\\/}-1)\\eqno(2)$$\nThe n dependence of the rate constants for Rydberg-atom destruction depends on the reactions involved. In reaction (1) the rate constant is independent of n whereas in reaction (2) it increases nearly linearly with n. When both reactions are possible, the measured n dependence can be explained in terms of contributions from each process.\nThe essentially-free-electron model suggests that the n dependence of the rate constants for Rydberg-atom destruction reflects the energy dependence of the cross sections of the corresponding free electron-molecule collision processes which are $$\\eqalignno{&e\\sp- + \\rm XY \\to (XY)\\sp{-*}\\ or\\ \\to X\\sp- + Y&(1\\sp\\prime)\\cr &e\\sp- + \\rm XY({\\it J\\/}) \\to {\\it e}\\sp- + XY({\\it J\\/}-1)&(2\\sp\\prime)\\cr}$$Analysis of the data therefore provides the behavior of cross sections for these processes at ultra-low electron energies.

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During the last two years, theoretical studies were performed on a variety of topics related to collisions involving Rydberg atoms. Progress was made towards the understanding of ion-Rydberg atom, Rydberg atom-Rydberg atom, and ground state atom-Rydberg atom collisions. Cross sections were calculated for electron capture, ionization, and excitation processes and parametrized in terms of atomic parameters. A strong dc electric field was also incoporated in calculations of electron capture and ionization cross sections for ion-Rydberg atom collisions. The results of this latter investigation indicate the design of a far ir photon detector which is based on the field ionization of Rydberg atoms may be limited by the collision processes. (Author)
In the present work very-high-n Rydberg-atoms (nsim100−nsim400)(n \\sim 100 - n \\sim 400)(nsim100−nsim400) are used to probe electron-molecule collisions at ultra-low electron energies. Based on the essentially-free-electron model, for sufficiently high n, Rydberg atom-molecule collisions can be described in terms of a binary interaction between the target molecule and the essentially-free Rydberg electron. Since the average kinetic energy of the Rydberg electron is ultra-low rm(sim85mueV−sim1.4meV),\\rm({\\sim}85\\mu eV - {\\sim}1.4meV),rm(sim85mueV−sim1.4meV), analysis of the very-high-n Rydberg-atom collision data can provide information on electron-molecule scattering at electron energies corresponding to electron temperatures of only $\\sim111\\sp\\circ$K, which are far below those accessible using any alternate approach.\nRate constants for destruction of very-high-n Rydberg atoms in collisions with various target molecules have been measured. This study focuses on Rydberg electron transfer to an electron-attaching molecule which results in negative ion formation via the reactions rmK(itnp/)+XYtoKsp++(XY)sp−∗ortoKsp++Xsp−+Yeqno(1)\\rm K({\\it np\\/}) + XY \\to K\\sp+ + (XY)\\sp{-*}\\ or\\ \\to K\\sp+ + X\\sp- + Y\\eqno(1)rmK(itnp/)+XYtoKsp++(XY)sp−∗ortoKsp++Xsp−+Yeqno(1)and on rotational energy transfer from polar molecules which leads to Rydberg atom ionization rmK(itnp/)+XY(itJ/)toKsp++itesp−+XY(itJ/−1)eqno(2)\\rm K({\\it np\\/}) + XY({\\it J\\/}) \\to K\\sp+ + {\\it e}\\sp- + XY({\\it J\\/}-1)\\eqno(2)rmK(itnp/)+XY(itJ/)toKsp++itesp−+XY(itJ/−1)eqno(2)\nThe n dependence of the rate constants for Rydberg-atom destruction depends on the reactions involved. In reaction (1) the rate constant is independent of n whereas in reaction (2) it increases nearly linearly with n. When both reactions are possible, the measured n dependence can be explained in terms of contributions from each process.\nThe essentially-free-electron model suggests that the n dependence of the rate constants for Rydberg-atom destruction reflects the energy dependence of the cross sections of the corresponding free electron-molecule collision processes which are $$\\eqalignno{&e\\sp- + \\rm XY \\to (XY)\\sp{-*}\\ or\\ \\to X\\sp- + Y&(1\\sp\\prime)\\cr &e\\sp- + \\rm XY({\\it J\\/}) \\to {\\it e}\\sp- + XY({\\it J\\/}-1)&(2\\sp\\prime)\\cr}$$Analysis of the data therefore provides the behavior of cross sections for these processes at ultra-low electron energies.