Abstract
Diblock copolymer thin films of polystyrene-block-poly(dimethyl siloxane)
(PS-b-PDMS) featuring PDMS cylinders in a PS matrix are investigated during
solvent vapor annealing with mixtures of n-heptane (which is strongly selective
for PDMS) and toluene (which is close to nonselective for both blocks).
Swelling in the vapor of one of the pure solvents and exchanging it stepwise by
the vapor of the other solvent is compared to swelling in a given binary solvent
vapor mixture for a prolonged time. The resulting structural changes, such as
ordering of the cylinders on a hexagonal lattice and their transition into lamellae, are followed using in situ, real-time grazing-incidence small-angle X-ray scattering (GISAXS). In three runs, the sequence of solvent vapor swelling and vapor exchange is varied. Compiling the resulting morphologies in a diagram of states in dependence on the solvent content in the film and in the minority nanodomains allows insight into the role of the glass transition of the PS matrix for the ordering processes and their time scales. Based on these findings, a protocol is suggested to efficiently obtain an order-to-order transition from the cylindrical morphology with random domain orientation to the oriented lamellar state.
(PS-b-PDMS) featuring PDMS cylinders in a PS matrix are investigated during
solvent vapor annealing with mixtures of n-heptane (which is strongly selective
for PDMS) and toluene (which is close to nonselective for both blocks).
Swelling in the vapor of one of the pure solvents and exchanging it stepwise by
the vapor of the other solvent is compared to swelling in a given binary solvent
vapor mixture for a prolonged time. The resulting structural changes, such as
ordering of the cylinders on a hexagonal lattice and their transition into lamellae, are followed using in situ, real-time grazing-incidence small-angle X-ray scattering (GISAXS). In three runs, the sequence of solvent vapor swelling and vapor exchange is varied. Compiling the resulting morphologies in a diagram of states in dependence on the solvent content in the film and in the minority nanodomains allows insight into the role of the glass transition of the PS matrix for the ordering processes and their time scales. Based on these findings, a protocol is suggested to efficiently obtain an order-to-order transition from the cylindrical morphology with random domain orientation to the oriented lamellar state.
Originalsprog | Engelsk |
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Artikelnummer | 2000150 |
Tidsskrift | Macromolecular Rapid Communications |
Vol/bind | 41 |
Udgave nummer | 14 |
Antal sider | 12 |
ISSN | 1022-1336 |
DOI | |
Status | Udgivet - 1 jul. 2020 |