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Size-Resolved Electron Solvation in Neutral Water Clusters

[Image: see text] Cluster-size-resolved ultrafast dynamics of the solvated electron in neutral water clusters with n = 3 to ∼200 molecules are studied with pump–probe time-of-flight mass spectrometry after below band gap excitation. For the smallest clusters, no longer-lived (>100–200 fs) hydrate...

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Autores principales: Ban, Loren, Yoder, Bruce L., Signorell, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237264/
https://www.ncbi.nlm.nih.gov/pubmed/34114470
http://dx.doi.org/10.1021/acs.jpca.1c03631
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author Ban, Loren
Yoder, Bruce L.
Signorell, Ruth
author_facet Ban, Loren
Yoder, Bruce L.
Signorell, Ruth
author_sort Ban, Loren
collection PubMed
description [Image: see text] Cluster-size-resolved ultrafast dynamics of the solvated electron in neutral water clusters with n = 3 to ∼200 molecules are studied with pump–probe time-of-flight mass spectrometry after below band gap excitation. For the smallest clusters, no longer-lived (>100–200 fs) hydrated electrons were detected, indicating a minimum size of n ∼ 14 for being able to sustain hydrated electrons. Larger clusters show a systematic increase of the number of hydrated electrons per molecule on the femtosecond to picosecond time scale. We propose that with increasing cluster size the underlying dynamics is governed by more effective electron formation processes combined with less effective electron loss processes, such as ultrafast hydrogen ejection and recombination. It appears unlikely that any size dependence of the solvent relaxation dynamics would be reflected in the observed time-resolved ion yields.
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spelling pubmed-82372642021-07-06 Size-Resolved Electron Solvation in Neutral Water Clusters Ban, Loren Yoder, Bruce L. Signorell, Ruth J Phys Chem A [Image: see text] Cluster-size-resolved ultrafast dynamics of the solvated electron in neutral water clusters with n = 3 to ∼200 molecules are studied with pump–probe time-of-flight mass spectrometry after below band gap excitation. For the smallest clusters, no longer-lived (>100–200 fs) hydrated electrons were detected, indicating a minimum size of n ∼ 14 for being able to sustain hydrated electrons. Larger clusters show a systematic increase of the number of hydrated electrons per molecule on the femtosecond to picosecond time scale. We propose that with increasing cluster size the underlying dynamics is governed by more effective electron formation processes combined with less effective electron loss processes, such as ultrafast hydrogen ejection and recombination. It appears unlikely that any size dependence of the solvent relaxation dynamics would be reflected in the observed time-resolved ion yields. American Chemical Society 2021-06-11 2021-06-24 /pmc/articles/PMC8237264/ /pubmed/34114470 http://dx.doi.org/10.1021/acs.jpca.1c03631 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Ban, Loren
Yoder, Bruce L.
Signorell, Ruth
Size-Resolved Electron Solvation in Neutral Water Clusters
title Size-Resolved Electron Solvation in Neutral Water Clusters
title_full Size-Resolved Electron Solvation in Neutral Water Clusters
title_fullStr Size-Resolved Electron Solvation in Neutral Water Clusters
title_full_unstemmed Size-Resolved Electron Solvation in Neutral Water Clusters
title_short Size-Resolved Electron Solvation in Neutral Water Clusters
title_sort size-resolved electron solvation in neutral water clusters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237264/
https://www.ncbi.nlm.nih.gov/pubmed/34114470
http://dx.doi.org/10.1021/acs.jpca.1c03631
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