Magnetic alignment of block copolymer microdomains by intrinsic chain anisotropy
Abstract
We examine the role of intrinsic chain susceptibility anisotropy in magnetic field directed self-assembly of a block copolymer using in situ x-ray scattering. Alignment of a lamellar mesophase is observed on cooling across the disorder-order transition with the resulting orientational order inversely proportional to the cooling rate. We discuss the origin of the susceptibility anisotropy, Δχ, that drives alignment and calculate its magnitude using coarse-grained molecular dynamics to sample conformations of surface-tethered chains, finding Δχ ≈ 2×10–8. From field-dependent scattering data, we estimate that grains of ≈ 1.2 μm are present during alignment. Furthermore, these results demonstrate that intrinsic anisotropy is sufficient to support strong field-induced mesophase alignment and suggest a versatile strategy for field control of orientational order in block copolymers.
- Authors:
-
- Yale Univ., New Haven, CT (United States)
- Brookhaven National Lab. (BNL), Upton, NY (United States)
- Univ. of Wisconsin, Madison, WI (United States)
- Publication Date:
- Research Org.:
- Brookhaven National Laboratory (BNL), Upton, NY (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1246786
- Alternate Identifier(s):
- OSTI ID: 1233966
- Report Number(s):
- BNL-111841-2016-JA
Journal ID: ISSN 0031-9007; PRLTAO; R&D Project: 16077; KC0403020
- Grant/Contract Number:
- SC00112704; SC0012704
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Physical Review Letters
- Additional Journal Information:
- Journal Volume: 115; Journal Issue: 25; Journal ID: ISSN 0031-9007
- Publisher:
- American Physical Society (APS)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 77 NANOSCIENCE AND NANOTECHNOLOGY
Citation Formats
Rokhlenko, Yekaterina, Yager, Kevin G., Gopinadhan, Manesh, Osuji, Chinedum O., Zhang, Kai, O'Hern, Corey S., Larson, Steven R., Gopalan, Padma, and Majewski, Pawel W. Magnetic alignment of block copolymer microdomains by intrinsic chain anisotropy. United States: N. p., 2015.
Web. doi:10.1103/PhysRevLett.115.258302.
Rokhlenko, Yekaterina, Yager, Kevin G., Gopinadhan, Manesh, Osuji, Chinedum O., Zhang, Kai, O'Hern, Corey S., Larson, Steven R., Gopalan, Padma, & Majewski, Pawel W. Magnetic alignment of block copolymer microdomains by intrinsic chain anisotropy. United States. https://doi.org/10.1103/PhysRevLett.115.258302
Rokhlenko, Yekaterina, Yager, Kevin G., Gopinadhan, Manesh, Osuji, Chinedum O., Zhang, Kai, O'Hern, Corey S., Larson, Steven R., Gopalan, Padma, and Majewski, Pawel W. Fri .
"Magnetic alignment of block copolymer microdomains by intrinsic chain anisotropy". United States. https://doi.org/10.1103/PhysRevLett.115.258302. https://www.osti.gov/servlets/purl/1246786.
@article{osti_1246786,
title = {Magnetic alignment of block copolymer microdomains by intrinsic chain anisotropy},
author = {Rokhlenko, Yekaterina and Yager, Kevin G. and Gopinadhan, Manesh and Osuji, Chinedum O. and Zhang, Kai and O'Hern, Corey S. and Larson, Steven R. and Gopalan, Padma and Majewski, Pawel W.},
abstractNote = {We examine the role of intrinsic chain susceptibility anisotropy in magnetic field directed self-assembly of a block copolymer using in situ x-ray scattering. Alignment of a lamellar mesophase is observed on cooling across the disorder-order transition with the resulting orientational order inversely proportional to the cooling rate. We discuss the origin of the susceptibility anisotropy, Δχ, that drives alignment and calculate its magnitude using coarse-grained molecular dynamics to sample conformations of surface-tethered chains, finding Δχ ≈ 2×10–8. From field-dependent scattering data, we estimate that grains of ≈ 1.2 μm are present during alignment. Furthermore, these results demonstrate that intrinsic anisotropy is sufficient to support strong field-induced mesophase alignment and suggest a versatile strategy for field control of orientational order in block copolymers.},
doi = {10.1103/PhysRevLett.115.258302},
journal = {Physical Review Letters},
number = 25,
volume = 115,
place = {United States},
year = {Fri Dec 18 00:00:00 EST 2015},
month = {Fri Dec 18 00:00:00 EST 2015}
}
Web of Science
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