Critical In-Plane Density of Polyelectrolyte Brush for the Ordered Hydrogen-Bonded Structure of Incorporated Water
A polymer electrolyte brush is a reasonable platform to confine water molecules within a nanoscopic area to study their role in the function of interacting media because of their adjustable nanospace and charge by changing the in-plane density and side chains of the brush. Here, we demonstrate how t...
Publié dans: | Langmuir : the ACS journal of surfaces and colloids. - 1985. - 38(2022), 10 vom: 15. März, Seite 3076-3081 |
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Auteur principal: | |
Autres auteurs: | , , , , |
Format: | Article en ligne |
Langue: | English |
Publié: |
2022
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Accès à la collection: | Langmuir : the ACS journal of surfaces and colloids |
Sujets: | Journal Article |
Résumé: | A polymer electrolyte brush is a reasonable platform to confine water molecules within a nanoscopic area to study their role in the function of interacting media because of their adjustable nanospace and charge by changing the in-plane density and side chains of the brush. Here, we demonstrate how the in-plane spacing of cationic polymer brush chains, poly[2-(methacryloyloxy)ethyltrimethylammonium chloride] (PMTAC), affects the hydrogen bond configuration of incorporated water using soft X-ray emission spectroscopy. At the critical in-plane density σ = 0.30 chains/nm2 of PMTAC, tetrahedrally coordinated water molecules started to melt into distorted or broken hydrogen-bonded configurations. Considering the charge on the quaternary ammonium cations, the electric field required to form a tetrahedrally coordinated hydrogen-bonded configuration was estimated as ∼500 kV cm-1 and is effective up to ∼1 nm from the surface of the polymer chain. These findings are useful for designing specific interface properties and the resultant surface function of polyelectrolyte-based materials |
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Description: | Date Revised 15.03.2022 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
ISSN: | 1520-5827 |
DOI: | 10.1021/acs.langmuir.1c02895 |