Structural analyses of sphere- and cylinder-forming triblock copolymer thin films near the free surface by atomic force microscopy, X-ray photoelectron spectroscopy, and grazing-incidence small-angle X-ray scattering

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorBayomi, Rasha Ahmed Hanafy
dc.contributor.authorAoki, Takashi
dc.contributor.authorShimojima, Takuma
dc.contributor.authorTakagi, Hideaki
dc.contributor.authorShimizu, Nobutaka
dc.contributor.authorIgarashi, Noriyuki
dc.contributor.authorSasaki, Sono
dc.contributor.authorSakurai, Shinichi
dc.date.accessioned2019-11-16T08:31:56Z
dc.date.available2019-11-16T08:31:56Z
dc.date.issued2018
dc.descriptionAccession Number: WOS:000436484100023en_US
dc.description.abstractWe investigated surface structures of three kinds of block copolymer (BCP) specimens forming hard spherical microdomains embedded in a soft matrix, by using atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and grazing-incidence small-angle X-ray scattering (GISAXS). The three BCP specimens consist of different chemical species such as SEBS (polystyrene-block-poly(ethylene-co-butylene)-block-polystyrene) and MAM (polymethylmethacrylate-block-poly(n-butylacrylate)-block-polymethylmethacrylate). Two of them form spherical microdomains at the thermodynamically equilibrium state (i.e., after fully long time thermal annealing), while the other exhibits spherical microdomains as a frozen state of the non-equilibrium structure (i.e., at the as-cast state using a selective solvent for the solution casting method), which was automatically frozen in by the vitrification of the hard component; the state is far from equilibrium). Nevertheless, such three different BCP specimens (chemically different in the molecular structure and thermodynamically different in the state) showed a common feature of the surface structure, as the outermost surface was completely covered with the single component having a lower value of the surface free energy, as revealed by XPS measurements. This finding significantly indicates that the AFM observation, which implies a coexistence of both BCP components on the free surface, misleads the conclusion. Although such surface coverage is reasonable and well-known, it was further found that the block chains are confined in a thin layer of the outermost region of the specimen. It is striking to find that the block chains are forced to be deformed (compressed) in order to meet the thermodynamic requirement of the surface coverage. (C) 2018 Elsevier Ltd. All rights reserved.en_US
dc.description.sponsorshipMinistry of Education, Culture, Sports, Science, and Technology of JapanMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)en_US
dc.identifier.doihttps://doi.org/10.1016/j.polymer.2018.05.074
dc.identifier.issn1873-2291
dc.identifier.otherhttps://doi.org/10.1016/j.polymer.2018.05.074
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0032386118304841
dc.language.isoenen_US
dc.publisherELSEVIER SCI LTDen_US
dc.relation.ispartofseriesPOLYMER;Volume: 147 Pages: 202-212
dc.relation.urihttps://cutt.ly/weGUQDU
dc.subjectUniversity of Block Copolymeren_US
dc.subjectX-ray photoelectron spectroscopyen_US
dc.subjectSpherical Microdomainen_US
dc.titleStructural analyses of sphere- and cylinder-forming triblock copolymer thin films near the free surface by atomic force microscopy, X-ray photoelectron spectroscopy, and grazing-incidence small-angle X-ray scatteringen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
avatar_scholar_256.png
Size:
6.31 KB
Format:
Portable Network Graphics
Description: