RAMAN-SCATTERING FROM SYSTEMS OF LINEAR-CHAIN MOLECULES (POLY(PROPYLENE OXIDE)) OF DIFFERENT LENGTHS - A COMPARISON WITH MOLECULAR-DYNAMICSSIMULATIONS

Citation
A. Brodin et al., RAMAN-SCATTERING FROM SYSTEMS OF LINEAR-CHAIN MOLECULES (POLY(PROPYLENE OXIDE)) OF DIFFERENT LENGTHS - A COMPARISON WITH MOLECULAR-DYNAMICSSIMULATIONS, Philosophical magazine. B. Physics of condensed matter.Statistical mechanics, electronic, optical and magnetic, 77(2), 1998, pp. 709-716
Citations number
16
Categorie Soggetti
Physics, Applied",Mechanics,"Physics, Condensed Matter","Material Science
ISSN journal
13642812
Volume
77
Issue
2
Year of publication
1998
Pages
709 - 716
Database
ISI
SICI code
1364-2812(1998)77:2<709:RFSOLM>2.0.ZU;2-D
Abstract
We present low-frequency Raman scattering results on CH3-terminated po ly(propylene oxide) of different molecular weights, corresponding to n = 1, 2, 7 and 70, n being the number of repeat units of the chains. T he results are compared with the density of states obtained from molec ular dynamics simulations of a similar set of systems (n = 1, 2 and 45 ). The measurements were performed over a temperature range (10-300K) covering the glass transition temperature. The low-frequency features typical of such systems, namely the boson peak (BP) and the disordered longitudinal acoustic mode (DLAM), were detected. We show that the sh ape and frequency position of the DLAM change dramatically with change in chain length, in accordance with theoretical models. In contrast, the shape and frequency position of the BP do not exhibit any strong n dependence, while its intensity increases on decreasing the chain len gth. The former observation suggests that BP reflects the collective d ynamics governed by intermolecular interactions within relatively larg e regions, such that the presence of additional correlations along the chains appears of little consequence. The behaviour of the intensity of the BP can qualitatively be explained by changes in the number of i ntermolecular degrees of freedom and by changes in the density of stat es.