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  Determining the radial distribution function of water using electron scattering: A key to solution phase chemistry

de Kock, M., Azim, S., Kassier, G., & Miller, R. J. D. (2020). Determining the radial distribution function of water using electron scattering: A key to solution phase chemistry. The Journal of Chemical Physics, 153(19): 194504. doi:10.1063/5.0024127.

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5.0024127.pdf (Publisher version), 2MB
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Open Access. - All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
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Supplemental: silicon_nitride_data (csv), water_data (csv)
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https://dx.doi.org/10.1063/5.0024127 (Publisher version)
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https://dx.doi.org/10.1063/10.0002830 (Supplementary material)
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Scilight Article "The shape – or structure – of water" by Anashe Bandari
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 Creators:
de Kock, M.1, Author           
Azim, S.1, Author           
Kassier, G.1, Author           
Miller, R. J. D.2, Author
Affiliations:
1Miller Group, Atomically Resolved Dynamics Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society, ou_1938288              
2Departments of Chemistry and Physics, University of Toronto, ou_persistent22              

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 Abstract: High energy electron scattering of liquid water (H2O) at near-ambient temperature and pressure was performed in a transmission electron microscope (TEM) to determine the radial distribution of water, which provides information on intra- and intermolecular spatial correlations. A recently developed environmental liquid cell enables formation of a stable water layer, the thickness of which is readily controlled by pressure and flow rate adjustments of a humid air stream passing between two silicon nitride (Si3N4) membranes. The analysis of the scattering data is adapted from the x-ray methodology to account for multiple scattering in the H2O:Si3N4 sandwich layer. For the H2O layer, we obtain oxygen–oxygen (O–O) and oxygen–hydrogen (O–H) peaks at 2.84 Å and 1.83 Å, respectively, in good agreement with values in the literature. This demonstrates the potential of our approach toward future studies of water-based physics and chemistry in TEMs or electron probes of structural dynamics.

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Language(s): eng - English
 Dates: 2020-08-052020-10-192020-11-202020-11-21
 Publication Status: Published in print
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 Rev. Type: Peer
 Identifiers: DOI: 10.1063/5.0024127
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Project name : The authors thank Djordje Gitaric and Josef Gonschior from the Atomic Resolved Dynamics department and the Machine Physics Scientific Support unit, both at the Max Planck Institute for the Structure and Dynamics of Matter in Hamburg, Germany, for their technical assistance. We also thank the Max Planck Society, Joachim Herz Foundation, and the Natural Sciences and Engineering Research Council of Canada (NSERC) for funding support.
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Title: The Journal of Chemical Physics
  Other : J. Chem. Phys.
Source Genre: Journal
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Publ. Info: Woodbury, N.Y. : American Institute of Physics
Pages: - Volume / Issue: 153 (19) Sequence Number: 194504 Start / End Page: - Identifier: ISSN: 0021-9606
CoNE: https://pure.mpg.de/cone/journals/resource/954922836226