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Direct Observation of the Phase Transition for a Poly(N-isopropylacryamide) Layer Grafted onto a Solid Surface by AFM and QCM-D

Year: 2007

Journal: Langmuir 2007, 23, 11083-11088, 20100827

Authors: Ishida N. † ‡, Biggs S * †

Last authors: Simon Biggs

Organizations: School of Process, Environmental and Materials Engineering, University of Leeds, Leeds LS2 9JT, United Kingdom, and Research Institute of Environmental Management Technology, National Institute of Advanced Industrial Science and Technology (AIST), 16-1 Onogawa, Tsukuba 306-8569, Japan

Country: Japan

The temperature-induced structural changes of a thermo-responsive poly(N-isopropylacrylamide) (PNIPAM) layer grafted onto a silica substrate were investigated in aqueous solution using an atomic force microscope (AFM) and a quartz crystal microbalance with dissipation (QCM-D). A PNIPAM layer was grafted onto the silicon wafer surface by free radical polymerization of NIPAM to obtain a high molecular weight polymer layer with low-grafting density overall. By AFM imaging, the transition of the grafted PNIPAM chains from a brush-like to a mushroom-like state was clearly visualized: The surface images of the plate were featureless at temperatures below the LCST commensurate with a brush-like layer, whereas above the LCST, a large number of domain structures with a characteristic size of ~100 nm were seen on the surface. Both frequency and dissipation data obtained using QCM-D showed a significant change at the LCST. Analysis of these data confirmed that the observed PNIPAM structural transition was caused by a collapse of the brush-like structure as a result of dehydration of the polymer chains.