Rotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogen

Rotationally resolved zero-kinetic-energy (ZEKE) photoelectron spectra of the X^2 Σ_(g)^(+) (V^(+) = 0,1)← X^(1)Σ_(g)^(+) (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...

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Main Authors: Merkt, F, Softley, T
Format: Journal article
Language:English
Published: American Physical Society 1992
Subjects:
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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^2 Σ_(g)^(+) (V^(+) = 0,1)← X^(1)Σ_(g)^(+) (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^(+) 0 J^(primeprime)) = +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^(+) 0 J^(primeprime)) = -2 and -4] intensity of the (O-O) band. Recording ZEKE spectra with extraction fields of 10-100V/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.
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spelling oxford-uuid:801b37c3-ce76-4b7c-8a0f-baced0ddd6612022-03-26T21:21:12ZRotationally resolved zero-kinetic-energy photoelectron spectrum of nitrogenJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:801b37c3-ce76-4b7c-8a0f-baced0ddd661Chemistry & allied sciencesPhysical & theoretical chemistryEnglishOxford University Research Archive - ValetAmerican Physical Society1992Merkt, FSoftley, TRotationally resolved zero-kinetic-energy (ZEKE) photoelectron spectra of the X^2 Σ_(g)^(+) (V^(+) = 0,1)← X^(1)Σ_(g)^(+) (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^(+) 0 J^(primeprime)) = +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^(+) 0 J^(primeprime)) = -2 and -4] intensity of the (O-O) band. Recording ZEKE spectra with extraction fields of 10-100V/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.
spellingShingle Chemistry & allied sciences
Physical & theoretical chemistry
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
topic Chemistry & allied sciences
Physical & theoretical chemistry
work_keys_str_mv AT merktf rotationallyresolvedzerokineticenergyphotoelectronspectrumofnitrogen
AT softleyt rotationallyresolvedzerokineticenergyphotoelectronspectrumofnitrogen