Block Copolymer Self-assembly on Ethylene Glycol (EG) Self-assembled Monolayer (SAM) for Nanofabrication

2012 ◽  
Vol 1450 ◽  
Author(s):  
Dipu Borah ◽  
Sozaraj Rasappa ◽  
Barbara Kosmala ◽  
Justin D. Holmes ◽  
Michael A. Morris

ABSTRACTNanostructure templates fabrication from P(S-b-MMA) thin films requires precise control of interfacial energies to achieve perpendicular orientation of microdomains to the substrate surface and can be obtained by modifying the oxide layer on silicon with a covalently anchored hydroxyl-terminated random copolymer P(S-r-MMA) termed a “neutral brush”. This commonly employed method enables precise fine-tuning of interfacial energies, but involves a lengthy process, requires starting materials that are commercially available but expensive, and results in a relatively thick under layer that can interfere with subsequent surface processing. We report here the microphase separation behaviour of an asymmetric P(S-b-MMA) diblock copolymer on electronic substrates modified with ethylene glycol (EG) self-assembled monolayer (SAM) as alternative to standard random copolymer brush. The diblock copolymer films deposited on EG SAMs upon thermal annealing spontaneously generates features with sub-lithographic resolution and pitch with perpendicular orientation. Selective etching provides a rapid route for the generation of PS template structures as the PMMA domains are etched at a faster rate. These templates can subsequently be used as etch masks to generate nanoscale features. We use state of the art lithography to generate sub-μm features and within these generate nm sized copolymer templates. Graphoepitaxy method proved a successful approach for the alignment of the microphase separated structures. This method of EG SAM driven self-0assembly provides a simple, rapid, yet tuneable approach for surface neutralization and nanofabrication technique for creating high density nanoscale features for the nanoelectronic industry.

Langmuir ◽  
2005 ◽  
Vol 21 (7) ◽  
pp. 2981-2987 ◽  
Author(s):  
Jonas Rundqvist ◽  
Jan H. Hoh ◽  
David B. Haviland

Author(s):  
Abigail N. Eldridge ◽  
Anna Dubnisheva ◽  
William H. Fissell ◽  
Aaaron J. Fleischman ◽  
Shuvo Roy

A Poly (ethylene glycol) (PEG) self-assembled monolayer was solution phase coupled to common MEMS (microelectromechanical systems) substrates through a one step procedure in order to investigate the potential anti-fouling properties of the polymer for implantable biomedical MEMS applications.


2016 ◽  
Vol 120 (29) ◽  
pp. 15915-15922 ◽  
Author(s):  
Thomas Doneux ◽  
Alexis de Ghellinck ◽  
Eléonore Triffaux ◽  
Nicolas Brouette ◽  
Michele Sferrazza ◽  
...  

2017 ◽  
Vol 8 (14) ◽  
pp. 2173-2181 ◽  
Author(s):  
Bing Yuan ◽  
Xin He ◽  
Yaqing Qu ◽  
Chengqiang Gao ◽  
Erika Eiser ◽  
...  

A diblock-copolymer/homopolymer self-assembled blend was synthesized through dispersion RAFT polymerization, and its morphology changed with a decreasing ratio of diblock-copolymer/homopolymer.


2021 ◽  
Vol 880 ◽  
pp. 114892
Author(s):  
Miriam Chávez ◽  
Guadalupe Sánchez-Obrero ◽  
Rafael Madueño ◽  
José Manuel Sevilla ◽  
Manuel Blázquez ◽  
...  

2000 ◽  
Vol 2 (8) ◽  
pp. 1729-1733 ◽  
Author(s):  
Alexander J. Pertsin ◽  
Michael Grunze ◽  
H. Jürgen Kreuzer ◽  
Richard L. C. Wang

1996 ◽  
Vol 461 ◽  
Author(s):  
Miri Park ◽  
Christopher Harrison ◽  
Paul M. Chaikin ◽  
Richard A. Register ◽  
Douglas Adamson ◽  
...  

ABSTRACTThe microphase separated morphology of diblock copolymers can be used to generate well-ordered nanometer scale patterns over a large area. To achieve this goal, it is important to understand and control the behavior of diblock copolymer thin films on substrates, which can differ from the bulk behavior. We have investigated the morphologies and ordering in thin polystyrene-polybutadiene (PS-PB) diblock copolymer films on bare silicon and silicon nitride substrates, and also on polymethylmethacrylate (PMMA) coated substrates. The PS-PB copolymers are synthesized to form, in bulk, PB cylinders or spheres in a PS matrix. In thin films (10–60 nm thick), prepared by spin-coating, we observe that the morphology and ordering of the microdomains are affected by strong wetting constraints and a reduced chain mobility on the substrate. The thinnest self-assembled layer of the copolymer films shows no in-plane microphase separation on both types of substrates. The PS blocks wet the PMMA substrates whereas the PB blocks wet the bare substrates as well as the air interface. Hence, different film thicknesses are necessary on the two types of substrates to obtain a uniform film of the first self-assembled cylindrical or spherical microdomain layer. The first layer of the cylindrical copolymer can vary from cylindrical to spherical morphology with a few nanometer decrease in film thickness. In the case of spherical PS-PB diblock copolymer films, we observe that the ordering of the microdomains is improved in the films on the PMMA substrates, compared to those on the bare substrates. We also demonstrate a successful transfer of the microdomain patterns to silicon nitride substrates by a reactive ion etching technique.


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