Issue 35, 2011

Radiolysis of astrophysical ice analogs by energetic ions: the effect of projectile mass and ice temperature

Abstract

An experimental study of the interaction of highly charged, energetic ions (52 MeV 58Ni13+ and 15.7 MeV 16O5+) with mixed H2O : C18O2 astrophysical ice analogs at two different temperatures is presented. This analysis aims to simulate the chemical and the physicochemical interactions induced by cosmic rays inside dense, cold astrophysical environments, such as molecular clouds or protostellar clouds as well at the surface of outer solar system bodies. The measurements were performed at the heavy ion accelerator GANIL (Grand Accelerateur National d'Ions Lourds) in Caen, France. The gas samples were deposited onto a CsI substrate at 13 K and 80 K. In situ analysis was performed by a Fourier transform infrared (FTIR) spectrometer at different fluences. Radiolysis yields of the produced species were quantified. The dissociation cross section at 13 K of both H2O and CO2 is about 3–4 times smaller when O ions are employed. The ice temperature seems to affect differently each species when the same projectile was employed. The formation cross section at 13 K of molecules such as C18O, CO (with oxygen from water), and H2O2 increases when Ni ions are employed. The formation of organic compounds seems to be enhanced by the oxygen projectiles and at lower temperatures. In addition, because the organic production at 13 K is at least 4 times higher than the value at 80 K, we also expect that interstellar ices are more organic-rich than the surfaces of outer solar system bodies.

Graphical abstract: Radiolysis of astrophysical ice analogs by energetic ions: the effect of projectile mass and ice temperature

Article information

Article type
Paper
Submitted
02 Mar 2011
Accepted
06 May 2011
First published
06 Jun 2011

Phys. Chem. Chem. Phys., 2011,13, 15755-15765

Radiolysis of astrophysical ice analogs by energetic ions: the effect of projectile mass and ice temperature

S. Pilling, E. S. Duarte, A. Domaracka, H. Rothard, P. Boduch and E. F. D. Silveira, Phys. Chem. Chem. Phys., 2011, 13, 15755 DOI: 10.1039/C1CP20592G

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