Repository logoCyprus University of Technology
Log In(current)
Ελληνικά
English
  1. Home
  2. Cyprus University of Technology (Research Output)
  3. Άρθρα/Articles
  4. Individual Contributions of Adsorbed and Free Chains to Microscopic Dynamics of Unentangled poly(ethylene Glycol)/Silica Nanocomposite Melts and the Important Role of End Groups: Theory and Simulation
  • Details

Individual Contributions of Adsorbed and Free Chains to Microscopic Dynamics of Unentangled poly(ethylene Glycol)/Silica Nanocomposite Melts and the Important Role of End Groups: Theory and Simulation

Journal
Macromolecules
Date Issued
May 25, 2021
Author(s)
Skountzos, Emmanuel N.  
Tsalikis, Dimitrios G.  
Stephanou, Pavlos S.  
Mavrantzas, Vlasis G.  
DOI
10.1021/acs.macromol.0c02485
Abstract
Molecular dynamics simulations and Rouse theory suitably adapted for polymer chains adsorbed by one or both of their ends are combined to offer a quantitative description of the local structure and microscopic dynamics in attractive polymer nanocomposite melts using a poly(ethylene glycol) (PEG)/silica nanocomposite as a model system. Our work reveals that the adsorbed layer around the silica nanoparticle is far from being characterized as "glassy"or "immobilized"since adsorbed polymer segments in the form of tails and loops on silica exhibit appreciable mobility locally, which helps adsorbed chains to relax at short length scales, albeit rather slowly. The simulations also reveal significant differences in the structural and dynamic properties of the PEG/silica nanocomposite melts studied for different terminal groups (hydroxyl versus methoxy) of the PEG chains, originating from the different ways that polymer chains adsorb on the silica surface: hydroxyl-terminated PEG chains are adsorbed by their ends giving rise to a brush-like structure, whereas methoxy-terminated ones are adsorbed equally probably along their entire contour, thus resulting in better packing of adsorbed segments. Due to the dense interfacial layer that develops in both cases, the diffusive behavior of free chains is also affected (it slows down compared to that in the corresponding pure PEG melt), especially in the nanocomposite where PEG chains are terminated with hydroxyl groups. Direct comparison of simulation and theoretical predictions with previously reported experimental data in the literature for the dynamic structure factor [Glomann et al., Phys. Rev. Lett. 2013, 110, 178001] for the same systems under the same temperature and pressure conditions reveals excellent agreement.
Subjects

Polymer molecular wei...

PEG matrix

Neutron Spin Eco

Early molecular dynam...

Explore by
  • Collections
  • Research Outputs
  • Researchers
  • Faculty & Departments
  • Theses
  • Patents
  • Projects
  • Journals
  • Conferences
Useful Links
  • Researcher Portfolio Guide
  • Researcher Profile
  • Create an ORCID ID
  • CUT Open Access Author Fund
  • ETDS Guide
Copyright Policies

Use Sherpa/Romeo to find publisher copyright policies

Go
Go
  • SPARC Author Addendum Engine
  • National Open Access Policy in Cyprus
Deposit your work to Ktisis
  • Self-archiving. Please sign in to Ktisis.
  • Email your work to:
    library.dspace@cut.ac.cy
  • Contact your subject librarian

Member of

OpenAIREre3dataOpenDOARCOREDART
Cyprus University of Technology
Library and
Information
Services

Copyright © 2022 - Library and Information Services Feedback - Built with DSpace-CRIS - 4Science

  • Accessibility settings
  • Privacy policy
  • End User Agreement
COAR NotifyCOAR Notify