Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-03T05:42:03.808Z Has data issue: false hasContentIssue false

5 - Photoionization dominated by double excitation in two-electron and divalent atoms

Published online by Cambridge University Press:  22 September 2009

J. J. Boyle
Affiliation:
Harvard University, Massachusetts
M. S. Pindzola
Affiliation:
Auburn University, Alabama
Get access

Summary

Introduction

Photoionization of a two-electron or a divalent atom in the vicinity of a doubly excited resonance due to the strong interaction between two outer electrons represents perhaps one of the most direct and unambiguous atomic processes for a quantitative study of the many-electron effects in atomic transitions. Recent applications of high resolution intense lasers and elaborate experiments in shorter wavelength regions with more advanced applications of synchrotron radiation to highly correlated atomic systems have opened up more opportunities for such a study. For example, operating at high synchrotron radiation intensity, Domke, Remmers, and Kaindl have recently observed the doubly-excited 2pnd1P series of He below the He+N = 2 threshold with an improved energy resolution of ≅ 4 meV. Parallel to the fast growing experimental advances, significant progress have also been made in many of the existing theoretical approaches.

One of the best known doubly excited photoionization structures is perhaps the He 2s2p1P resonance shown in Fig. 5.1. This resonance was first observed in detail by Madden and Codling in He photoionization from its ground state and classified subsequently by Cooper, Fano, and Prats. Theoretically, the photoionization structure of an isolated resonance located at resonant energy Er is best described by the Fano formula in terms of a set of resonant parameters, which includes the resonance width Γ, the asymmetry parameter q, and the nonresonant background cross section σb.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×