PMSE Alshakim Nelson, Matthew Becker, Sergio Granados-Focil, Christopher Stafford  Wednesday, March 19, 2014 

336 - Directed self assembly of block copolymer thin films with dynamic thermal annealing and flexible interfaces

Alamgir Karim1, alamgir@uakron.edu, Gurpreet Singh2, Arzu Hayirlioglu1, Ren Zhang1, Arvind Modi1, Kevin Yager3. (1) Department of Polymer Engineering, University of Akron, Akron, OH 44325, United States, (2) Lithography Materials, IBM Almaden Research Center, Almaden, San Jose 95120, United States, (3) Condensed Soft Matter Group, Brookhaven National Laboratory, Brookhaven, New York, United States

Orientation control of block copolymer (BCP) films is important for advanced technological applications. We present studies on directed ordering of block copolymer thin films on rigid substrates such as quartz to elastomeric PDMS and flexible Kapton substrates for tunable orientation of microphase separated poly (styrene) – block -poly (methylmethacrylate) (PS-PMMA) cylinder and lamellae forming BCP films. Although the crosslinked PDMS has low surface energy, its surface energy can be tuned by exposing to UV-Ozone (UVO) that presents an opportunity to change BCP-PDMS interfacial energy to control BCP orientation across full range of orientation and film wettability. On the other hand, Kapton offers a near neutral surface for PS-PMMA without surface modification. Via a modified version of a dynamic thermal processing termed “cold zone annealing-sharp (CZA-S) ”, we obtain a wide range of orientations of the block copolymer films in unfilled and nanoparticle filled systems with an interest in photovoltaic systems. With CZA-S, vertical orientation of PS-PMMA can be obtained in films as thick as 1 micron with etchable PMMA domains for membrane applications. GISAXS characterization of these etched BCP membranes reveals up to 5 orders of diffraction indicating hexagonally packed vertical nanopores that extend throughout the film. Under similar thermal gradient, but static conditions, temporally stable vertical cylinders form only within a narrow zone of maximum temperature gradient. Primary CZA-S ordering mechanism thus involves propagating this narrow vertically oriented zone of BCP cylinders created at the maximum thermal gradient section, across the film. An optimal speed is needed since the process competes with preferential surface wetting dynamics that favors parallel orientation. These results are reproduced on large area flexible films on a prototype dynamic R2R assembly platform with incorporated multi-CZA gradient for thin (~100 nm) BCP films currently. Recent efforts to apply these design principles for membranes and polymer solar cell design will be discussed.


Wednesday, March 19, 2014 10:30 AM
Structure for Function: Rational Design of New Functional Polymeric Materials (08:30 AM - 12:00 PM)
Location: Hyatt Regency Dallas
Room: Cumberland F

 

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