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  Electron-Induced Synthesis of Ozone in a Dioxygen Matrix

Lacombe, S., Cemic, F., Jacobi, K., Hedhili, M. N., Le Coat, Y., Azria, R., et al. (1997). Electron-Induced Synthesis of Ozone in a Dioxygen Matrix. Physical Review Letters, 79(6), 1146-1149. doi:10.1103/PhysRevLett.79.1146.

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PhysRevLett.79.1146.pdf (Publisher version), 101KB
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PhysRevLett.79.1146.pdf
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1997
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APS
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 Creators:
Lacombe, S.1, Author           
Cemic, F.1, Author           
Jacobi, Karl2, Author           
Hedhili, M. N.3, Author
Le Coat, Y.3, Author
Azria, R.3, Author
Tronc, M.4, Author
Affiliations:
1Fritz Haber Institute, Max Planck Society, ou_24021              
2Physical Chemistry, Fritz Haber Institute, Max Planck Society, ou_634546              
3Laboratoire des Collisions Atomiques et Moléculaires, Université Paris-Sud , Bâtiment 351, 91405 Orsay, France, ou_persistent22              
4Laboratoire de Chimie Physique-Matière et Rayonnement, Université Pierre et Marie Curie, 75231 Paris Cedex 05, France, ou_persistent22              

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 Abstract: Ozone (O3) was synthesized in the condensed phase induced by electron bombardment of multilayer films of molecular oxygen condensed at temperatures below 30 K on metal surfaces. O3 formation
was demonstrated by the observation of the asymmetric stretching (v3) and bending (v2) normal modes
of vibration in a high-resolution electron energy-loss spectroscopy experiment, and by characteristic changes in electron-stimulated desorption of O-. The threshold electron energy for the O3 formation is found at 3.5±0,2 eV. It corresponds to the formation of O(3P) associated with O-(2P) by dissociative
electron attachment at condensed O2, followed by the third body reaction O+O2 +O2→O3+O2. Above 5.1 eV bombarding energy, dissociative excitation of the O̊̇̑2̑
(c1Σu
-,C3Δu,A3Σu+
,B3Σu-) states is the main source of atomic oxygen O(3P) or O(1D) involved in the O3 synthesis.

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Language(s): eng - English
 Dates: 1997-02-281997-08-11
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1103/PhysRevLett.79.1146
 Degree: -

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Title: Physical Review Letters
  Abbreviation : Phys. Rev. Lett.
Source Genre: Journal
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Publ. Info: Woodbury, N.Y. : American Physical Society
Pages: 4 Volume / Issue: 79 (6) Sequence Number: - Start / End Page: 1146 - 1149 Identifier: ISSN: 0031-9007
CoNE: https://pure.mpg.de/cone/journals/resource/954925433406_1