Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.

Rotationally resolved zero-kinetic-energy (ZEKE) photoelectron spectra of the X g+2(v+=0,1) X g+1(v=0) bands of nitrogen have been recorded. The spectra show unexpected rotational-line intensities. The intensity distortions are explained by channel interactions. The strong S and U branches [(N+-J)=+...

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Main Authors: Merkt, F, Softley, T
Format: Journal article
Language:English
Published: 1992
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author Merkt, F
Softley, T
author_facet Merkt, F
Softley, T
author_sort Merkt, F
collection OXFORD
description Rotationally resolved zero-kinetic-energy (ZEKE) photoelectron spectra of the X g+2(v+=0,1) X g+1(v=0) bands of nitrogen have been recorded. The spectra show unexpected rotational-line intensities. The intensity distortions are explained by channel interactions. The strong S and U branches [(N+-J)=+2 and +4, respectively] of the (1-0) band borrow intensity from a nearly degenerate Rydberg state, converging to an electronic excited state of the ion, by a complex resonance mechanism. Field-induced rotational autoionization is shown to enhance the O branch and M branch [(N+-J)=-2 and -4] intensity of the (0-0) band. Recording ZEKE spectra with extraction fields of 10100 V/cm appears to be an attractive and powerful way of obtaining spectroscopic information on Rydberg states with simultaneously high principal quantum number n and high total-angular-momentum quantum number J. © 1992 The American Physical Society.
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spelling oxford-uuid:95209c21-5484-4aab-abe4-6de711f009c12022-03-26T23:44:00ZRotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:95209c21-5484-4aab-abe4-6de711f009c1EnglishSymplectic Elements at Oxford1992Merkt, FSoftley, TRotationally resolved zero-kinetic-energy (ZEKE) photoelectron spectra of the X g+2(v+=0,1) X g+1(v=0) bands of nitrogen have been recorded. The spectra show unexpected rotational-line intensities. The intensity distortions are explained by channel interactions. The strong S and U branches [(N+-J)=+2 and +4, respectively] of the (1-0) band borrow intensity from a nearly degenerate Rydberg state, converging to an electronic excited state of the ion, by a complex resonance mechanism. Field-induced rotational autoionization is shown to enhance the O branch and M branch [(N+-J)=-2 and -4] intensity of the (0-0) band. Recording ZEKE spectra with extraction fields of 10100 V/cm appears to be an attractive and powerful way of obtaining spectroscopic information on Rydberg states with simultaneously high principal quantum number n and high total-angular-momentum quantum number J. © 1992 The American Physical Society.
spellingShingle Merkt, F
Softley, T
Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.
title Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.
title_full Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.
title_fullStr Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.
title_full_unstemmed Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.
title_short Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen.
title_sort rotationally resolved zero kinetic energy photoelectron spectrum of nitrogen
work_keys_str_mv AT merktf rotationallyresolvedzerokineticenergyphotoelectronspectrumofnitrogen
AT softleyt rotationallyresolvedzerokineticenergyphotoelectronspectrumofnitrogen