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Polymers on Nanoperiodic, Heterogeneous Surfaces
Author(s) -
L. Rockford,
Y. Liu,
P. Mansky,
Thomas P. Russell,
M. Yoon,
S. G. J. Mochrie
Publication year - 1999
Publication title -
physical review letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.688
H-Index - 673
eISSN - 1079-7114
pISSN - 0031-9007
DOI - 10.1103/physrevlett.82.2602
Subject(s) - polymer , materials science , copolymer , lamellar structure , nanoscopic scale , substrate (aquarium) , chemical physics , oxide , phase (matter) , molecule , macromolecule , surface (topology) , length scale , chemical engineering , nanotechnology , composite material , chemistry , geometry , organic chemistry , biochemistry , oceanography , mathematics , geology , engineering , metallurgy , physics , quantum mechanics
Herein we establish a relationship between controlled nanoscale surface interactions and subsequent macromolecular ordering. Striped surfaces of oxide and metal are generated over large areas, where the stripe width is comparable to the size of a polymer molecule. Homopolymers are found to anisotropically dewet such surfaces, while incompatible polymer mixtures phase separate at the substrate/polymer interface on a molecular level. An orientation of lamellar block copolymer microdomains normal to the surface is found, when substrate and polymer length scales are commensurate. {copyright} {ital 1999} {ital The American Physical Society}

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