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Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous Solid Water at Low Temperatures
[Image: see text] Mixtures of methanol and amorphous solid water (ASW) ices are observed in the interstellar medium (ISM), where they are subject to irradiation by UV photons and bombardment by charged particles. The charged particles, if at high enough density, induce a local electric field in the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948533/ https://www.ncbi.nlm.nih.gov/pubmed/36763094 http://dx.doi.org/10.1021/acs.langmuir.2c03441 |
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author | Akerman, Michelle Sykes Iny, Hiley Sagi, Roey Asscher, Micha |
author_facet | Akerman, Michelle Sykes Iny, Hiley Sagi, Roey Asscher, Micha |
author_sort | Akerman, Michelle Sykes |
collection | PubMed |
description | [Image: see text] Mixtures of methanol and amorphous solid water (ASW) ices are observed in the interstellar medium (ISM), where they are subject to irradiation by UV photons and bombardment by charged particles. The charged particles, if at high enough density, induce a local electric field in the ice film that potentially affects the photochemistry of these ices. When CD(3)OD@ASW ices grown at 38 K on a Ru(0001) substrate are irradiated by 193 nm (6.4 eV) photons, products such as HD, D(2), CO, and CO(2) are formed in large abundances relative to the initial amount of CD(3)OD. Other molecules such as D(2)O, CD(4), acetaldehyde, and ethanol and/or dimethyl ether are also observed, but in smaller relative abundances. The reactivity cross sections range from (2.6 ± 0.3) × 10(–21) to (3.8 ± 0.3) × 10(–25) cm(2)/photon. The main products are formed through two competing mechanisms: direct photodissociation of methanol and water and dissociative electron attachment (DEA) by photoelectrons ejected from the Ru(0001) substrate. An electric field of 2 × 10(8) V/m generated within the ASW film during Ne(+) ions bombardment is apparently not strong enough to affect the relative abundances (selectivity) of the photochemical products observed in this study. |
format | Online Article Text |
id | pubmed-9948533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99485332023-02-24 Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous Solid Water at Low Temperatures Akerman, Michelle Sykes Iny, Hiley Sagi, Roey Asscher, Micha Langmuir [Image: see text] Mixtures of methanol and amorphous solid water (ASW) ices are observed in the interstellar medium (ISM), where they are subject to irradiation by UV photons and bombardment by charged particles. The charged particles, if at high enough density, induce a local electric field in the ice film that potentially affects the photochemistry of these ices. When CD(3)OD@ASW ices grown at 38 K on a Ru(0001) substrate are irradiated by 193 nm (6.4 eV) photons, products such as HD, D(2), CO, and CO(2) are formed in large abundances relative to the initial amount of CD(3)OD. Other molecules such as D(2)O, CD(4), acetaldehyde, and ethanol and/or dimethyl ether are also observed, but in smaller relative abundances. The reactivity cross sections range from (2.6 ± 0.3) × 10(–21) to (3.8 ± 0.3) × 10(–25) cm(2)/photon. The main products are formed through two competing mechanisms: direct photodissociation of methanol and water and dissociative electron attachment (DEA) by photoelectrons ejected from the Ru(0001) substrate. An electric field of 2 × 10(8) V/m generated within the ASW film during Ne(+) ions bombardment is apparently not strong enough to affect the relative abundances (selectivity) of the photochemical products observed in this study. American Chemical Society 2023-02-10 /pmc/articles/PMC9948533/ /pubmed/36763094 http://dx.doi.org/10.1021/acs.langmuir.2c03441 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Akerman, Michelle Sykes Iny, Hiley Sagi, Roey Asscher, Micha Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous Solid Water at Low Temperatures |
title | Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming
Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous
Solid Water at Low Temperatures |
title_full | Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming
Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous
Solid Water at Low Temperatures |
title_fullStr | Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming
Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous
Solid Water at Low Temperatures |
title_full_unstemmed | Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming
Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous
Solid Water at Low Temperatures |
title_short | Chemical Reactivity of Strongly Interacting, Hydrogen-Bond-Forming
Molecules Following 193 nm Photon Irradiation: Methanol in Amorphous
Solid Water at Low Temperatures |
title_sort | chemical reactivity of strongly interacting, hydrogen-bond-forming
molecules following 193 nm photon irradiation: methanol in amorphous
solid water at low temperatures |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948533/ https://www.ncbi.nlm.nih.gov/pubmed/36763094 http://dx.doi.org/10.1021/acs.langmuir.2c03441 |
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