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Confinement and Processing Can Alter the Morphology and Periodicity of Bottlebrush Block Copolymers in Thin Films

Sunday, Daniel F. and Dolejsi, Moshe and Chang, Alice B. and Richter, Lee J. and Li, Ruipeng and Kline, R. Joseph and Nealey, Paul F. and Grubbs, Robert H. (2020) Confinement and Processing Can Alter the Morphology and Periodicity of Bottlebrush Block Copolymers in Thin Films. ACS Nano, 14 (12). pp. 17476-17486. ISSN 1936-0851. https://resolver.caltech.edu/CaltechAUTHORS:20201123-142123886

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Abstract

Bottlebrush block copolymers (BBCPs) are intriguing architectural variations on linear BCPs with highly tunable structure. Confinement can have a significant impact on polymer assembly, giving rise to changes in morphology, assembly kinetics, and properties like the glass transition. Given that confinement leads to significant changes in the persistence length of bottlebrush homopolymers, it is reasonable to expect that BBCPs will see significant changes in their structure and periodicity relative to the bulk morphology. Understanding how confinement influences assembly will be important for designing BBCPs for thin film applications including membranes, integrated photonic structures, and potentially BCP lithography. In order to study the effects of confinement on BBCP conformation and morphology, a blade coating was used to prepare films with continuous variation in film thickness. Unlike thin films of linear BCPs, islands/holes were not observed, and instead mixtures of parallel and perpendicular morphologies emerge after annealing. The lamellar periodicity (L₀) of the morphologies is found to be thickness dependent, increasing L₀ with decreasing film thickness for blade coated films. Films coated out of tetrahydrofuran (THF) resulted in a single well-defined lamellar periodicity, verified through atomic force microscopy (AFM) and grazing incidence small-angle X-ray scattering (GISAXS), which increases dramatically from the bulk value (30.6 nm) and continues to increase as the film thickness decreases. The largest observed L₀ was 65.5 nm, and this closely approaches the estimated upper limit of 67 nm corresponding to a fully extended backbone in a bilayer arrangement. Films coated out of propylene glycol methyl ether acetate (PGMEA) resulted in a mixture of perpendicular lamellae and a smaller, likely cylindrical morphology. The lamellar portion of the film shows the same thickness dependence as the lamellae observed in the THF coated films. The scaling of the lamellar L₀ with respect to film thickness follows predictions for confined semiflexible polymers with weak excluded volume interactions and can be related to models for confinement of DNA. Spin coated films shows the same reduction in periodicity, although at very different film thicknesses. This result suggests that the material has shallow free-energy barriers to transitioning between different L₀ and morphologies, a property that could be taken advantage of for patterning diverse structures with a single material.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1021/acsnano.0c07777DOIArticle
ORCID:
AuthorORCID
Sunday, Daniel F.0000-0002-6840-535X
Chang, Alice B.0000-0001-5036-2681
Richter, Lee J.0000-0002-9433-3724
Nealey, Paul F.0000-0003-3889-142X
Grubbs, Robert H.0000-0002-0057-7817
Additional Information:© 2020 American Chemical Society. Received: September 15, 2020; Accepted: November 17, 2020; Published: November 23, 2020. The authors would like to thank Kathryn Beers and Jack Douglass for helpful discussions. Portions of this work were performed at the DuPont–Northwestern–Dow Collaborative Access Team (DND-CAT) located at Sector 5 of the Advanced Photon Source (APS). DND-CAT is supported by E. I. DuPont de Nemours & Co., The Dow Chemical Company and Northwestern University. Use of the APS, an Office of Science User Facility operated for the US Department of Energy (DOE) Office of Science by Argonne National Laboratory, was supported by the US DOE under contract No. DE-AC02-06CH11357. We thank Steven Weigand and Denis Keane for assistance at sector 5-ID-D. The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under contract no. DE-AC02-05CH11231. We thank Cheng Wang for assistance at BL 11.0.1.2 This research used resources CMS beamline of the National Synchrotron Light Source II, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under Contract No. DE-SC0012704. The project was in part funded by award no. 70NHNB14H012 from the U.S. Department of Commerce, National Institute of Standards and Technology, as part of the Center for Hierarchical Materials Design (CHiMaD). The authors declare no competing financial interest.
Funders:
Funding AgencyGrant Number
E. I. DuPont de Nemours and Company, Inc.UNSPECIFIED
Dow Chemical CompanyUNSPECIFIED
Northwestern UniversityUNSPECIFIED
Department of Energy (DOE)DE-AC02-06CH11357
Department of Energy (DOE)DE-AC02-05CH11231
Department of Energy (DOE)DE-SC0012704
Department of Commerce70NHNB14H012
National Institute of Standards and Technology (NIST)UNSPECIFIED
Subject Keywords:bottlebrush, block copolymer, confinement, thin film, self-assembly, saxs, gisaxs
Issue or Number:12
Record Number:CaltechAUTHORS:20201123-142123886
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20201123-142123886
Official Citation:Confinement and Processing Can Alter the Morphology and Periodicity of Bottlebrush Block Copolymers in Thin Films. Daniel F. Sunday, Moshe Dolejsi, Alice B. Chang, Lee J. Richter, Ruipeng Li, R. Joseph Kline, Paul F. Nealey, and Robert H. Grubbs. ACS Nano 2020 14 (12), 17476-17486; DOI: 10.1021/acsnano.0c07777
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:106793
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:23 Nov 2020 22:53
Last Modified:05 Jan 2021 22:26

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