Sub-10-nm patterning via directed self-assembly of block copolymer films with a vapour-phase deposited topcoat
Author(s) -
Hyo Seon Suh,
Do Han Kim,
Priya Moni,
Shisheng Xiong,
Leonidas E. Ocola,
Nestor J. Zaluzec,
Karen K. Gleason,
Paul F. Nealey
Publication year - 2017
Publication title -
nature nanotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 14.308
H-Index - 353
eISSN - 1748-3395
pISSN - 1748-3387
DOI - 10.1038/nnano.2017.34
Subject(s) - copolymer , materials science , chemical vapor deposition , polymer , thin film , phase (matter) , nanotechnology , substrate (aquarium) , deposition (geology) , chemical engineering , composite material , chemistry , organic chemistry , paleontology , oceanography , sediment , geology , engineering , biology
Directed self-assembly (DSA) of the domain structure in block copolymer (BCP) thin films is a promising approach for sub-10-nm surface patterning. DSA requires the control of interfacial properties on both interfaces of a BCP film to induce the formation of domains that traverse the entire film with a perpendicular orientation. Here we show a methodology to control the interfacial properties of BCP films that uses a polymer topcoat deposited by initiated chemical vapour deposition (iCVD). The iCVD topcoat forms a crosslinked network that grafts to and immobilizes BCP chains to create an interface that is equally attractive to both blocks of the underlying copolymer. The topcoat, in conjunction with a chemically patterned substrate, directs the assembly of the grating structures in BCP films with a half-pitch dimension of 9.3 nm. As the iCVD topcoat can be as thin as 7 nm, it is amenable to pattern transfer without removal. The ease of vapour-phase deposition, applicability to high-resolution BCP systems and integration with pattern-transfer schemes are attractive properties of iCVD topcoats for industrial applications.
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