Nanophase separation and structural evolution of block copolymer films: a "green" and "clean" supercritical fluid approach

No Thumbnail Available
Files
4727_Ghoshal_et_al_BCP-SCF.pdf(1.14 MB)
Submitted version
Date
2014-11-18
Authors
Ghoshal, Tandra
Biswas, Subhajit
O'Regan, Colm
Holmes, Justin D.
Morris, Michael A.
Journal Title
Journal ISSN
Volume Title
Publisher
Tsinghua University Press and Springer Verlag
Research Projects
Organizational Units
Journal Issue
Abstract
Thin films of block copolymers (BCPs) are widely accepted as potentially important materials in a host of technological applications including nanolithography. In order to induce domain separation and form well-defined structural arrangements, many of these are solvent-annealed (i.e. solvent swollen) at moderate temperatures. The use of solvents can be challenging in industry from an environmental point of view as well as having practical/cost issues. However, a simple and environmentally friendly alternative to solvo-thermal annealing for the periodically ordered nanoscale phase separated structures is described herein. Various asymmetric polystyrene-b-poly(ethylene oxide) (PS-b-PEO) thin films were annealed in a compressible fluid, supercritical carbon dioxide (scCO2), to control nanodomain orientation and surface morphologies. For the first time, periodic well defined, hexagonally ordered films with sub-25 nm pitch size were demonstrated using a supercritical fluid (SCF) process at low temperatures and pressures. Predominant swelling of PEO domains in scCO2 induces nanophase separation. scCO2 serves as green alternative to the conventional organic solvents for the phase segregation of BCPs with complete elimination of any residual solvent in the patterned film. The depressurization rate of scCO2 following annealing was found to affect the morphology of the films. The supercritical annealing conditions could be used to define nanoporous analogues of the microphase separated films without additional processing, providing a one-step route to membrane like structures without affecting the ordered surface phase segregated structure. An understanding of the BCP self-assembly mechanism can be realized in terms of the deviation in glass transition temperature, melting point, viscosity, interaction parameter and volume fraction of the constituent blocks in the scCO2 environment.
Description
Keywords
Block copolymer , Supercritical CO2 , Self-assembly , Swelling , Nanopores
Citation
Ghoshal, T., Biswas, S., O’Regan, C., Holmes, J. D. and Morris, M. A. (2015) 'Nanophase separation and structural evolution of block copolymer films: A “green” and “clean” supercritical fluid approach', Nano Research, 8(4), pp. 1279-1292. doi: 10.1007/s12274-014-0616-7
Copyright
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2014. This is a pre-print of an article published in Nano Research. The final authenticated version is available online at: https://doi.org/10.1007/s12274-014-0616-7