Interaction of water with oligo(ethylene glycol) terminated monolayers: wetting versus hydration

Biorepulsivity of oligo(ethylene glycol) (OEG) substituted self-assembled monolayers (SAMs), serving as model systems for analogous polymeric surfaces, is generally ascribed to the hydration effect. In this context, we applied temperature-programmed desorption to study interaction of water (D2O) wit...

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Hauptverfasser: Sayın, Mustafa (VerfasserIn) , Nefedov, Alexei (VerfasserIn) , Zharnikov, Michael (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 27 Mar 2020
In: Physical chemistry, chemical physics
Year: 2020, Jahrgang: 22, Heft: 15, Pages: 8088-8095
ISSN:1463-9084
DOI:10.1039/D0CP00906G
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1039/D0CP00906G
Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/2020/cp/d0cp00906g
Volltext
Verfasserangaben:Mustafa Sayin, Alexei Nefedov and Michael Zharnikov

MARC

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520 |a Biorepulsivity of oligo(ethylene glycol) (OEG) substituted self-assembled monolayers (SAMs), serving as model systems for analogous polymeric surfaces, is generally ascribed to the hydration effect. In this context, we applied temperature-programmed desorption to study interaction of water (D2O) with a series of OH-terminated, OEG-substituted alkanethiolate SAMs with variable length of the OEG strand, defining their biorepulsion behavior. Along with the ice overlayer (wetting phase), growing also on the surface of the analogous non-substituted films, a hydration phase, corresponding to the adsorption of D2O into the OEG matrix, was observed, with a higher desorption energy (12.4 kcal mol−1vs. 10.4 kcal mol−1) and a weight correlating with the length of the OEG strand and, consequently, with biorepulsivity. The formation of hydration phase was found to occur over an activation barrier, presumably by temperature-promoted diffusion from the wetting phase, with this process being additionally enforced by a pre-desorption annealing. 
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