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Solution Structure and Hydration Forces between Mica and Hydrophilic Versus Hydrophobic Surfaces
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    C: Physical Properties of Materials and Interfaces

    Solution Structure and Hydration Forces between Mica and Hydrophilic Versus Hydrophobic Surfaces
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    • E. Nakouzi*
      E. Nakouzi
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      *Email: [email protected]
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    • S. Kerisit
      S. Kerisit
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      More by S. Kerisit
    • B. A. Legg
      B. A. Legg
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      More by B. A. Legg
    • S. Yadav
      S. Yadav
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      More by S. Yadav
    • D. Li
      D. Li
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      More by D. Li
    • A. G. Stack
      A. G. Stack
      Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
      More by A. G. Stack
    • C. J. Mundy
      C. J. Mundy
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      Department of Materials Science and Engineering, University of Washington, Seattle, Washington 98195, United States
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    • J. Chun
      J. Chun
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      Department of Chemical Engineering, CUNY City College of New York, New York, New York 10031, United States
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    • G. K. Schenter
      G. K. Schenter
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      Department of Chemistry, Washington State University, Pullman, Washington 99164, United States
    • J. J. De Yoreo*
      J. J. De Yoreo
      Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      Department of Materials Science and Engineering, University of Washington, Seattle, Washington 98195, United States
      *Email: [email protected]
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    The Journal of Physical Chemistry C

    Cite this: J. Phys. Chem. C 2023, 127, 5, 2741–2752
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    https://doi.org/10.1021/acs.jpcc.2c09120
    Published January 26, 2023
    Copyright © 2023 American Chemical Society

    Abstract

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    Solid–liquid interfaces are central to a range of interesting phenomena including colloidal aggregation, crystallization by particle attachment, catalysis, heterogeneous nucleation, water desalination, and biomolecular assembly. While three-dimensional atomic force microscopy (3D AFM) has emerged as a technique for resolving interfacial solution structure at the molecular scale, key challenges for data interpretation persist, most notably regarding the influence of the probe on the measured structure. Using the mica–water system as a case study, we investigate the effect of hydrophilic and hydrophobic probes on interfacial solution structure measured by 3D AFM. Data from hydrophilic silicon-based probes are in good agreement with molecular dynamics simulations, wherein the innermost water molecules adsorb preferentially at the surface ditrigonal cavity sites, followed by two additional ordered hydration layers. In contrast, the hydrophobic carbon-based probes detect vertical oscillatory features but do not show lateral patterning that matches the underlying mica lattice. At high ionic strength, up to six of these oscillatory features are observed extending 2 nm into the solution phase with an average spacing of 0.29 ± (0.04) nm. We also determine that the repulsive hydration force between mica and the hydrophilic probe depends on the nature and concentration of ions in solution. Specifically, solutions with stronger ion–water and ion–ion interactions produce a stronger repulsive hydration force as the probe approaches the surface. Based on these observations, we present a scheme for controlling the outcomes of particle aggregation and attachment by varying the solution conditions to tune the hydration force.

    Copyright © 2023 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.jpcc.2c09120.

    • Supporting 3D AFM and MD data and tables describing the parameters used in the MD simulations (PDF)

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    Most electronic Supporting Information files are available without a subscription to ACS Web Editions. Such files may be downloaded by article for research use (if there is a public use license linked to the relevant article, that license may permit other uses). Permission may be obtained from ACS for other uses through requests via the RightsLink permission system: http://pubs.acs.org/page/copyright/permissions.html.

    Cited By

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    This article is cited by 5 publications.

    1. Pravalika Butreddy, Jaeyoung Heo, Nikhil Rampal, Tingting Liu, Lili Liu, William Smith, Xin Zhang, Micah P. Prange, Benjamin A. Legg, Gregory K. Schenter, James J. De Yoreo, Jaehun Chun, Andrew G. Stack, Elias Nakouzi. Ion Correlations Decrease Particle Aggregation Rate by Increasing Hydration Forces at Interfaces. ACS Nano 2024, 18 (38) , 26047-26055. https://doi.org/10.1021/acsnano.4c05563
    2. Kazuki Miyata, Kosuke Adachi, Naoyuki Miyashita, Keisuke Miyazawa, Adam S. Foster, Takeshi Fukuma. High-Speed Three-Dimensional Scanning Force Microscopy Visualization of Subnanoscale Hydration Structures on Dissolving Calcite Step Edges. Nano Letters 2024, 24 (35) , 10842-10849. https://doi.org/10.1021/acs.nanolett.4c02368
    3. Lili Liu, Sakshi Yadav Schmid, Zhaojie Feng, Dongsheng Li, Timothy C. Droubay, Peter J. Pauzauskie, Gregory K. Schenter, James J. De Yoreo, Jaehun Chun, Elias Nakouzi. Effect of Solvent Composition on Non-DLVO Forces and Oriented Attachment of Zinc Oxide Nanoparticles. ACS Nano 2024, 18 (26) , 16743-16751. https://doi.org/10.1021/acsnano.4c01797
    4. Tingting Liu, Nikhil Rampal, Elias Nakouzi, Benjamin A. Legg, Jaehun Chun, Lili Liu, Gregory K. Schenter, James J. De Yoreo, Lawrence M. Anovitz, Andrew G. Stack. Molecular Mechanisms of Sorbed Ion Effects during Boehmite Particle Aggregation. Langmuir 2024, 40 (17) , 8791-8805. https://doi.org/10.1021/acs.langmuir.3c03532
    5. Jonathan G. Hedley, Hélène Berthoumieux, Alexei A. Kornyshev. The Dramatic Effect of Water Structure on Hydration Forces and the Electrical Double Layer. The Journal of Physical Chemistry C 2023, 127 (18) , 8429-8447. https://doi.org/10.1021/acs.jpcc.3c00262

    The Journal of Physical Chemistry C

    Cite this: J. Phys. Chem. C 2023, 127, 5, 2741–2752
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acs.jpcc.2c09120
    Published January 26, 2023
    Copyright © 2023 American Chemical Society

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