Solvation dynamics of molecular glass-forming liquids in confinement

Ranko Richert, Min Yang

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Triplet state solvation dynamics experiments on geometrically confined glass-forming liquids are performed in order to study the effects of confinement on length scales of several nanometres. Variations of the surface chemistry of porous glasses and the spatially selective observation of the interfacial liquid layer indicate that the surface interactions determine the difference between the dynamics of the bulk and confined situations. For 3-methylpentane in pores of 7.5 nm diameter, the timescale of interfacial dynamics is slowed down by three orders of magnitude, while structural relaxation already remains bulk-like just a few nanometres away from the silica surface. The time-resolved optical linewidths indicate dynamical heterogeneity in confined liquids, but the signature differs from the bulk case.

Original languageEnglish (US)
JournalJournal of Physics Condensed Matter
Volume15
Issue number11
DOIs
StatePublished - Mar 26 2003

Fingerprint

Solvation
solvation
Glass
glass
Liquids
liquids
Structural relaxation
Surface chemistry
Silicon Dioxide
Linewidth
surface reactions
atomic energy levels
Silica
signatures
chemistry
silicon dioxide
porosity
Experiments

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics

Cite this

Solvation dynamics of molecular glass-forming liquids in confinement. / Richert, Ranko; Yang, Min.

In: Journal of Physics Condensed Matter, Vol. 15, No. 11, 26.03.2003.

Research output: Contribution to journalArticle

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