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Título

Neutron spectroscopy as a probe of macromolecular structure and dynamics under extreme spatial confinement

AutorBarroso-Bujans, Fabienne ; Fernández-Alonso, Félix; Colmenero de León, Juan
Fecha de publicación2014
EditorInstitute of Physics Publishing
CitaciónJournal of Physics: Conference Series 549: 012009 (2014)
ResumenWe illustrate the use of high-resolution neutron spectroscopy to explore the extreme spatial confinement of soft matter in nanostructured materials. Two well-defined limits are considered, involving either intercalation or interfacial adsorption of the ubiquitous polymer poly(ethylene oxide) in graphite-oxide-based hosts. Vibrational modes associated with the confined macromolecular phase undergo dramatic changes over a broad range of energy transfers, from those associated with intermolecular modes in the Terahertz frequency range (1 THz = 33 cm−1), to those characteristic of strong chemical bonds above 2000 cm−1. We also consider the effects of polymer chain size and chemical composition of the host material. Variation of the degree of oxidation and exfoliation of graphite oxide leads to two distinct cases, namely: (i) subnanometer two-dimensional confinement; and (ii) surface immobilization. Case (i) is characterised by significant changes to conformational and collective vibrational modes of the polymer as a consequence of a preferentially planar trans-trans-trans chain conformation, whereas case (ii) leads to a substantial increase in the population of gauche conformers. Macroscopically, case (i) translates into the complete suppression of crystallization and glassy behaviour. In contrast, case (ii) exhibits well-defined glass and melting transitions associated with the confined phase, yet at significantly lower temperatures than those of the bulk.
Descripción6th Meeting of the Spanish Neutron Scattering Association (SETN2012).
Versión del editorhttp://dx.doi.org/10.1088/1742-6596/549/1/012009
URIhttp://hdl.handle.net/10261/137043
DOI10.1088/1742-6596/549/1/012009
Identificadoresdoi: 10.1088/1742-6596/549/1/012009
issn: 1742-6588
e-issn: 1742-6596
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