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Journal article

The 193nm photolysis of NO2: NO(v) vibrational distribution, O(D-1) quantum yield and emission from vibrationally excited NO2

Abstract:: Time resolved Fourier transform infrared emission has been used to study the photolysis of NO2 and its dimer N2O4 at 193 nm. NO(ν) populations from the photolysis of NO2 show a bimodal distribution, peaking at ν = 5 and with a subsidiary maximum at ν = 14, close to the energetically allowed limit. The results are discussed in terms of previous measurements near this photolysis wavelength of the kinetic energies of the two possible O atomic fragments, O(3P) and O(1D), and on the electronic sta...
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Publication status:: Published

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APA Style

Hancock, G., & Morrison, M. (2005). The 193nm photolysis of NO2: NO(v) vibrational distribution, O(D-1) quantum yield and emission from vibrationally excited NO2. MOLECULAR PHYSICS, 103(13), 1727–1733.

MLA Style

Hancock, G., and M. Morrison. “The 193nm Photolysis of NO2: NO(v) Vibrational Distribution, O(D-1) Quantum Yield and Emission from Vibrationally Excited NO2.” MOLECULAR PHYSICS, vol. 103, no. 13, 2005, pp. 1727–33.

Chicago Style

Hancock, G, and M Morrison. 2005. “The 193nm Photolysis of NO2: NO(v) Vibrational Distribution, O(D-1) Quantum Yield and Emission from Vibrationally Excited NO2.” MOLECULAR PHYSICS 103 (13): 1727–33.
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Publisher copy:: 10.1080/00268970500086161

Authors

+ Hancock, G More by this author

Institution:

University of Oxford

Division:

MPLS

Department:

Chemistry

Sub department:

Physical & Theoretical Chem

Role:

Author

+ Morrison, M More by this author

Role:

Author

Bibliographic Details

Journal:: MOLECULAR PHYSICS
Volume:: 103
Issue:: 13
Pages:: 1727-1733
Publication date:: 2005-07-10
DOI:: 10.1080/00268970500086161
EISSN:: 1362-3028
ISSN:: 0026-8976

Item Description

Language:: English
Pubs id:: pubs:39554
UUID:: uuid:679eb282-3f98-4377-ad37-57fec1305970
Local pid:: pubs:39554
Source identifiers:: 39554
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2005

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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