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Wavelength-dependent UV photodesorption of pure N2 and O2 ices.

Authors :
Fayolle, E. C.
Bertin, M.
Romanzin, C.
Poderoso, H. A. M.
Philippe, L.
Michaut, X.
Jeseck, P.
Linnartz, H.
Öberg, K. I.
Fillion, J.-H.
Source :
Astronomy & Astrophysics / Astronomie et Astrophysique; Aug2013, Vol. 556 Issue 6, p1-7, 7p
Publication Year :
2013

Abstract

Context. Ultraviolet photodesorption of molecules from icy interstellar grains can explain observations of cold gas in regions where thermal desorption is negligible. This non-thermal desorption mechanism should be especially important where UV fluxes are high. Aims. N<subscript>2</subscript> and O<subscript>2</subscript> are expected to play key roles in astrochemical reaction networks, both in the solid state and in the gas phase. Measurements of the wavelength-dependent photodesorption rates of these two infrared-inactive molecules provide astronomical and physical-chemical insights into the conditions required for their photodesorption. Methods. Tunable radiation from the DESIRS beamline at the SOLEIL synchrotron in the astrophysically relevant 7 to 13.6 eV range is used to irradiate pure N<subscript>2</subscript> and O<subscript>2</subscript> thin ice films. Photodesorption of molecules is monitored through quadrupole mass spectrometry. Absolute rates are calculated by using the well-calibrated CO photodesorption rates. Strategic N<subscript>2</subscript> and O<subscript>2</subscript> isotopolog mixtures are used to investigate the importance of dissociation upon irradiation. Results. N<subscript>2</subscript> photodesorption mainly occurs through excitation of the b<superscript>1</superscript>Π<subscript>u</subscript> state and subsequent desorption of surface molecules. The observed vibronic structure in the N<subscript>2</subscript> photodesorption spectrum, together with the absence of N<subscript>3</subscript> formation, supports that the photodesorption mechanism of N<subscript>2</subscript> is similar to CO, i.e., an indirect DIET (Desorption Induced by Electronic Transition) process without dissociation of the desorbing molecule. In contrast, O<subscript>2</subscript> photodesorption in the 7-13.6 eV range occurs through dissociation and presents no vibrational structure. Conclusions. Photodesorption rates of N<subscript>2</subscript> and O<subscript>2</subscript> integrated over the far-UV field from various star-forming environments are lower than for CO. Rates vary between 10<superscript>-3</superscript> and 10<superscript>-2</superscript> photodesorbed molecules per incoming photon. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00046361
Volume :
556
Issue :
6
Database :
Complementary Index
Journal :
Astronomy & Astrophysics / Astronomie et Astrophysique
Publication Type :
Academic Journal
Accession number :
89749706
Full Text :
https://doi.org/10.1051/0004-6361/201321533