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Host-Guest Self-assembly in Block Copolymer Blends

Journal Article · · Scientific Reports
DOI:https://doi.org/10.1038/srep03190· OSTI ID:1624669
 [1];  [2];  [3];  [3];  [3];  [3];  [3];  [4];  [2];  [3]
  1. Korea Advanced Inst. Science and Technology (KAIST), Daejeon (Korea, Republic of). Dept. of Materials Science and Engineering; DOE/OSTI
  2. Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Materials Science and Engineering
  3. Korea Advanced Inst. Science and Technology (KAIST), Daejeon (Korea, Republic of). Dept. of Materials Science and Engineering
  4. Rice Univ., Houston, TX (United States). Dept. of Mechanical Engineering and Materials Science
Ultrafine, uniform nanostructures with excellent functionalities can be formed by self-assembly of block copolymer (BCP) thin films. However, extension of their geometric variability is not straightforward due to their limited thin film morphologies. Here, we report that unusual and spontaneous positioning between host and guest BCP microdomains, even in the absence of H-bond linkages, can create hybridized morphologies that cannot be formed from a neat BCP. Our self-consistent field theory (SCFT) simulation results theoretically support that the precise registration of a spherical BCP microdomain (guest, B-b-C) at the center of a perforated lamellar BCP nanostructure (host, A-b-B) can energetically stabilize the blended morphology. As an exemplary application of the hybrid nanotemplate, a nanoring-type Ge2Sb2Te5 (GST) phase-change memory device with an extremely low switching current is demonstrated. These results suggest the possibility of a new pathway to construct more diverse and complex nanostructures using controlled blending of various BCPs.
Research Organization:
Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
SC0001088
OSTI ID:
1624669
Journal Information:
Scientific Reports, Journal Name: Scientific Reports Journal Issue: 1 Vol. 3; ISSN 2045-2322
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English

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Self-Assembly in ultrahigh molecular weight sphere-forming diblock copolymer thin films under strong confinement collection January 2019
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Individual Confinement of Block Copolymer Microdomains in Nanoscale Crossbar Templates journal December 2018
Self‐Assembled Asymmetric Block Copolymer Membranes: Bridging the Gap from Ultra‐ to Nanofiltration journal September 2015
Self-Assembled Asymmetric Block Copolymer Membranes: Bridging the Gap from Ultra- to Nanofiltration journal September 2015
Non-native three-dimensional block copolymer morphologies journal December 2016
Self-Assembly in ultrahigh molecular weight sphere-forming diblock copolymer thin films under strong confinement journal December 2019
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