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Published on: June 30, 2018
Lithographically Defined Cross-Linkable Top Coats for Nanomanufacturing with High-χ Block Copolymers
Xavier Chevalier1, Cindy Gomes Correia2, Gwenaelle Pound-Lana3
1ARKEMA FRANCE, GRL, Route Nationale 117, BP34 64170 Lacq, France.
Novel top-coat materials enable directed self-assembly (DSA) of block copolymers (BCPs). This approach suppresses dewetting and controls domain orientation for high-resolution nanostructures, overcoming key manufacturing challenges.
Area of Science:
- Materials Science
- Nanotechnology
- Polymer Chemistry
Background:
- Directed self-assembly (DSA) of block copolymers (BCPs) is crucial for manufacturing high-resolution nanofeatures.
- Challenges include dewetting, controlled domain orientation, and precise spatial positioning of BCP features.
- Existing methods require further optimization for reliable large-scale implementation.
Purpose of the Study:
- To introduce novel top-coat (TC) materials for enhanced DSA of BCPs.
- To address critical issues of dewetting and domain orientation in BCP self-assembly.
- To enable controlled, localized patterning of BCP nanostructures.
Main Methods:
- Development of novel top-coat (TC) materials capable of thermal or photo-triggered cross-linking.
- Application of TC layer to BCPs, inducing mechanical confinement and suppressing dewetting.
- Utilizing lithography on the patternable TC layer for selective area processing and feature registration.
Main Results:
- Cross-linked TC layer effectively suppresses dewetting of the underlying BCP layer.
- The TC material promotes perpendicular orientation of BCP domains.
- Patternable TC allows for lithographic selection of areas with desired perpendicular BCP features.
Conclusions:
- Novel cross-linkable TC materials offer a viable solution for controlling BCP dewetting and orientation.
- The developed method enables precise, localized generation of BCP patterns and multilayers.
- This approach presents attractive integration pathways for advanced nanomanufacturing applications.
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