Segmental dynamics of polymers in 1 and 2nm slit-pores

Research output: Contribution to journalConference article

Abstract

Molecular dynamics computer simulations are used to study the structure and dynamics of 1nm wide films of poly(ethylene oxide) (PEO) confined between mica type layered silicates of different cation exchange capacities(CEC). The simulation setup mimics the experimental systems formed by intercalation of PEO in silicate clays with differing numbers of inherent charges. Counterbalancing lithium cations are present in the interlayer gallery to offset the negative charge on the silicate platelets created by the isomorphic substitution of trivalent aluminum by divalent magnesium ions. It is seen that the presence of the lithium has a significance influence on the behavior of the system, with PEO segmental motion strongly dependent on the number of Li+ present in the slit pore. In particular, the coexistence of fast and slow modes for C-H bond dynamics is heavily affected due to the strong interaction between the Li+ ions and partially charged PEO oxygen. In conjunction with local density inhomogeneities, the coordination between lithium and oxygen is responsible for the anomalous segmental dynamics of nanoconfined PEO.

Original languageEnglish (US)
Pages (from-to)47-52
Number of pages6
JournalMaterials Research Society Symposium - Proceedings
Volume790
StatePublished - Dec 1 2003
EventDynamics in Small Confining Systems - 2003 - Boston, MA, United States
Duration: Dec 1 2003Dec 4 2003

Fingerprint

Polyethylene oxides
slits
silicates
Polymers
lithium
porosity
Silicates
polymers
Lithium
cations
oxygen
ethylene oxide
platelets
mica
intercalation
clays
Cations
magnesium
interlayers
ions

All Science Journal Classification (ASJC) codes

  • Materials Science(all)
  • Condensed Matter Physics
  • Mechanics of Materials
  • Mechanical Engineering

Cite this

@article{c32b18b4b3e3409aaf084beaaaaabbdd,
title = "Segmental dynamics of polymers in 1 and 2nm slit-pores",
abstract = "Molecular dynamics computer simulations are used to study the structure and dynamics of 1nm wide films of poly(ethylene oxide) (PEO) confined between mica type layered silicates of different cation exchange capacities(CEC). The simulation setup mimics the experimental systems formed by intercalation of PEO in silicate clays with differing numbers of inherent charges. Counterbalancing lithium cations are present in the interlayer gallery to offset the negative charge on the silicate platelets created by the isomorphic substitution of trivalent aluminum by divalent magnesium ions. It is seen that the presence of the lithium has a significance influence on the behavior of the system, with PEO segmental motion strongly dependent on the number of Li+ present in the slit pore. In particular, the coexistence of fast and slow modes for C-H bond dynamics is heavily affected due to the strong interaction between the Li+ ions and partially charged PEO oxygen. In conjunction with local density inhomogeneities, the coordination between lithium and oxygen is responsible for the anomalous segmental dynamics of nanoconfined PEO.",
author = "V. Kuppa and Evangelos Manias",
year = "2003",
month = "12",
day = "1",
language = "English (US)",
volume = "790",
pages = "47--52",
journal = "Materials Research Society Symposium - Proceedings",
issn = "0272-9172",
publisher = "Materials Research Society",

}

Segmental dynamics of polymers in 1 and 2nm slit-pores. / Kuppa, V.; Manias, Evangelos.

In: Materials Research Society Symposium - Proceedings, Vol. 790, 01.12.2003, p. 47-52.

Research output: Contribution to journalConference article

TY - JOUR

T1 - Segmental dynamics of polymers in 1 and 2nm slit-pores

AU - Kuppa, V.

AU - Manias, Evangelos

PY - 2003/12/1

Y1 - 2003/12/1

N2 - Molecular dynamics computer simulations are used to study the structure and dynamics of 1nm wide films of poly(ethylene oxide) (PEO) confined between mica type layered silicates of different cation exchange capacities(CEC). The simulation setup mimics the experimental systems formed by intercalation of PEO in silicate clays with differing numbers of inherent charges. Counterbalancing lithium cations are present in the interlayer gallery to offset the negative charge on the silicate platelets created by the isomorphic substitution of trivalent aluminum by divalent magnesium ions. It is seen that the presence of the lithium has a significance influence on the behavior of the system, with PEO segmental motion strongly dependent on the number of Li+ present in the slit pore. In particular, the coexistence of fast and slow modes for C-H bond dynamics is heavily affected due to the strong interaction between the Li+ ions and partially charged PEO oxygen. In conjunction with local density inhomogeneities, the coordination between lithium and oxygen is responsible for the anomalous segmental dynamics of nanoconfined PEO.

AB - Molecular dynamics computer simulations are used to study the structure and dynamics of 1nm wide films of poly(ethylene oxide) (PEO) confined between mica type layered silicates of different cation exchange capacities(CEC). The simulation setup mimics the experimental systems formed by intercalation of PEO in silicate clays with differing numbers of inherent charges. Counterbalancing lithium cations are present in the interlayer gallery to offset the negative charge on the silicate platelets created by the isomorphic substitution of trivalent aluminum by divalent magnesium ions. It is seen that the presence of the lithium has a significance influence on the behavior of the system, with PEO segmental motion strongly dependent on the number of Li+ present in the slit pore. In particular, the coexistence of fast and slow modes for C-H bond dynamics is heavily affected due to the strong interaction between the Li+ ions and partially charged PEO oxygen. In conjunction with local density inhomogeneities, the coordination between lithium and oxygen is responsible for the anomalous segmental dynamics of nanoconfined PEO.

UR - http://www.scopus.com/inward/record.url?scp=2942662006&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=2942662006&partnerID=8YFLogxK

M3 - Conference article

AN - SCOPUS:2942662006

VL - 790

SP - 47

EP - 52

JO - Materials Research Society Symposium - Proceedings

JF - Materials Research Society Symposium - Proceedings

SN - 0272-9172

ER -