Normal Modes and Dielectric Spectra of Diblock Copolymers in Lamellar Phases

Vaidyanathan Sethuraman, Victor Pryamitsyn, Venkat Ganesan

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

We use molecular dynamics simulations to study the normal mode dynamics and frequency dependent dielectric relaxation spectra of diblock copolymers in lamellar phases. In contrast to previous works which have relied on the applicability of Rouse modes, we effect an explicit normal-mode analysis of the chain dynamics in the ordered phases in the directions parallel and perpendicular to the lamellar plane. We considered two models to isolate the specific effects arising from the morphological ordering and mobility disparities between the blocks. For systems with no mobility disparity between the blocks, our analysis demonstrates that both the normal modes and their relaxation dynamics in the planes parallel and perpendicular to the lamella exhibit deviations from the Rouse modes. For systems in which the mobility of one of the blocks was frozen in the lamellar phase, the normal modes closely resembled the Rouse modes for tethered polymers. However, the relaxation dynamics of such modes exhibited deviations from expectations for tethered chains. The changes in the normal mode dynamics manifest as shifts and broadening of the normal dielectric spectra. Together, our results serve to clarify the dielectric spectra effects resulting from the ordering of diblock copolymers into self-assembled morphologies.

Original languageEnglish (US)
Pages (from-to)2821-2831
Number of pages11
JournalMacromolecules
Volume49
Issue number7
DOIs
StatePublished - Apr 26 2016

Bibliographical note

Funding Information:
The work was supported by grants from Robert A. Welch Foundation (Grant F1599) and National Science Foundation (DMR-1306844) and the US Army Research Office under Grant W911NF-13-1-0396. The authors acknowledge the Texas Advanced Computing Center (TACC) for computing resources.

Publisher Copyright:
© 2016 American Chemical Society.

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