Pattern formation mechanisms in sphere-forming diblock copolymer thin films

The order-disorder transition of a sphere-forming block copolymer thin film was numerically studied through a Cahn-Hilliard model. Simulations show that the fundamental mechanisms of pattern formation are spinodal decomposition and nucleation and growth. The range of validity of each relaxation proc...

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Main Authors: Leopoldo R. Gómez, Nicolás A. García, Richard A. Register, Daniel A. Vega
Format: Article
Language:English
Published: Papers in Physics 2018-01-01
Series:Papers in Physics
Subjects:
Online Access:http://www.papersinphysics.org/papersinphysics/article/view/405/pdf405
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spelling doaj-97ee536740524ddb9975ab2ab94621782020-11-24T21:42:08ZengPapers in PhysicsPapers in Physics1852-42491852-42492018-01-0110010000110.4279/PIP.100001Pattern formation mechanisms in sphere-forming diblock copolymer thin filmsLeopoldo R. GómezNicolás A. GarcíaRichard A. RegisterDaniel A. VegaThe order-disorder transition of a sphere-forming block copolymer thin film was numerically studied through a Cahn-Hilliard model. Simulations show that the fundamental mechanisms of pattern formation are spinodal decomposition and nucleation and growth. The range of validity of each relaxation process is controlled by the spinodal and order-disorder temperatures. The initial stages of spinodal decomposition are well approximated by a linear analysis of the evolution equation of the system. In the metastable region, the critical size for nucleation diverges upon approaching the order--disorder transition, and reduces to the size of a single domain as the spinodal is approached. Grain boundaries and topological defects inhibit the formation of superheated phases above the order--disorder temperature. The numerical results are in good qualitative agreement with experimental data on sphere-forming diblock copolymer thin films. Received: 22 August 2017, Accepted: 12 December 2017; Edited by: R. Dickman; Reviewed by: A. Peters, Dept. Chemical Engineering, Louisiana Tech Univ., Ruston, USA; DOI: http://dx.doi.org/10.4279/PIP.100001 Cite as: L R Gómez, N A García, R A Register, D A Vega, Papers in Physics 10, 100001 (2018) This paper, by L R Gómez, N A García, R A Register, D A Vega, is licensed under the Creative Commons Attribution License 4.0.http://www.papersinphysics.org/papersinphysics/article/view/405/pdf405Block CopolymerThin FilmsPhase TransitionSelf-assembly
collection DOAJ
language English
format Article
sources DOAJ
author Leopoldo R. Gómez
Nicolás A. García
Richard A. Register
Daniel A. Vega
spellingShingle Leopoldo R. Gómez
Nicolás A. García
Richard A. Register
Daniel A. Vega
Pattern formation mechanisms in sphere-forming diblock copolymer thin films
Papers in Physics
Block Copolymer
Thin Films
Phase Transition
Self-assembly
author_facet Leopoldo R. Gómez
Nicolás A. García
Richard A. Register
Daniel A. Vega
author_sort Leopoldo R. Gómez
title Pattern formation mechanisms in sphere-forming diblock copolymer thin films
title_short Pattern formation mechanisms in sphere-forming diblock copolymer thin films
title_full Pattern formation mechanisms in sphere-forming diblock copolymer thin films
title_fullStr Pattern formation mechanisms in sphere-forming diblock copolymer thin films
title_full_unstemmed Pattern formation mechanisms in sphere-forming diblock copolymer thin films
title_sort pattern formation mechanisms in sphere-forming diblock copolymer thin films
publisher Papers in Physics
series Papers in Physics
issn 1852-4249
1852-4249
publishDate 2018-01-01
description The order-disorder transition of a sphere-forming block copolymer thin film was numerically studied through a Cahn-Hilliard model. Simulations show that the fundamental mechanisms of pattern formation are spinodal decomposition and nucleation and growth. The range of validity of each relaxation process is controlled by the spinodal and order-disorder temperatures. The initial stages of spinodal decomposition are well approximated by a linear analysis of the evolution equation of the system. In the metastable region, the critical size for nucleation diverges upon approaching the order--disorder transition, and reduces to the size of a single domain as the spinodal is approached. Grain boundaries and topological defects inhibit the formation of superheated phases above the order--disorder temperature. The numerical results are in good qualitative agreement with experimental data on sphere-forming diblock copolymer thin films. Received: 22 August 2017, Accepted: 12 December 2017; Edited by: R. Dickman; Reviewed by: A. Peters, Dept. Chemical Engineering, Louisiana Tech Univ., Ruston, USA; DOI: http://dx.doi.org/10.4279/PIP.100001 Cite as: L R Gómez, N A García, R A Register, D A Vega, Papers in Physics 10, 100001 (2018) This paper, by L R Gómez, N A García, R A Register, D A Vega, is licensed under the Creative Commons Attribution License 4.0.
topic Block Copolymer
Thin Films
Phase Transition
Self-assembly
url http://www.papersinphysics.org/papersinphysics/article/view/405/pdf405
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