TY - JOUR
T1 - Oxygen as an Electron Scavenger
T2 - Its Role in Electron-Induced Activation of Coadsorbed Methane Embedded in Amorphous Solid Water
AU - Ramakrishnan, Sujith
AU - Sagi, Roey
AU - Sorek, Elishama
AU - Methikkalam, Rabin Rajan J.
AU - Asscher, Micha
N1 - Publisher Copyright:
Copyright © 2018 American Chemical Society.
PY - 2019/4/4
Y1 - 2019/4/4
N2 - Low-energy electrons are known to play a fundamental role in activating small molecules in interstellar chemistry. Here we illustrate the electron-induced activation of the inert molecule methane while sandwiched between two 50 monolayers thick layers of amorphous solid water (ASW) on ruthenium substrate at 25 K by employing externally supplied low-energy electrons (5 eV) under ultrahigh vacuum conditions. We demonstrate how electron transmission through ASW layers under cryogenic conditions is strongly affected in the presence of cosandwiched oxygen molecules. We conclude that the resonant nature and direct electron attachment process leads to a higher degree of conversion in the presence of embedded oxygen molecules along with methane. Cross sections ranging from 1 × 10 -18 to 1 × 10 -19 cm 2 /electrons were obtained from the post-irradiation temperature-programmed desorption spectra.
AB - Low-energy electrons are known to play a fundamental role in activating small molecules in interstellar chemistry. Here we illustrate the electron-induced activation of the inert molecule methane while sandwiched between two 50 monolayers thick layers of amorphous solid water (ASW) on ruthenium substrate at 25 K by employing externally supplied low-energy electrons (5 eV) under ultrahigh vacuum conditions. We demonstrate how electron transmission through ASW layers under cryogenic conditions is strongly affected in the presence of cosandwiched oxygen molecules. We conclude that the resonant nature and direct electron attachment process leads to a higher degree of conversion in the presence of embedded oxygen molecules along with methane. Cross sections ranging from 1 × 10 -18 to 1 × 10 -19 cm 2 /electrons were obtained from the post-irradiation temperature-programmed desorption spectra.
UR - http://www.scopus.com/inward/record.url?scp=85054397360&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.8b06388
DO - 10.1021/acs.jpcc.8b06388
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AN - SCOPUS:85054397360
SN - 1932-7447
VL - 123
SP - 7766
EP - 7775
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 13
ER -