Mapping water uptake in organic coatings using AFM-IR.

The long-term failure of seemingly intact corrosion resistant organic coatings is thought to occur via the development of ionic transport channels, which spontaneously evolve from hydrophilic regions on immersion, i.e., as a result of localized water uptake. To this end, we investigate water uptake characteristics for industrial epoxy-phenolic can coatings after immersion in deionized water and drying. Moisture sorption and the changing nature of polymer-water interactions are assessed using FTIR for dry and pre-soaked films. More water is found to be absorbed by the pre-soaked coatings on exposure to a humid environment, with a greater degree of hydrogen-bonding between the polymer and water. Furthermore, morphological changes are then correlated to localized water uptake using the AFM-IR technique. Nanoscale softened regions develop on soaking, and these are found to absorb a greater proportion of water from a humid environment.

Tailoring the density of surface-tethered bottlebrushes.

Surface-tethered bottlebrushes have been prepared by ATRP grafting of the macroinitiator brush backbone onto plasmachemical-deposited poly(vinylbenzyl chloride) initiator nanofilms followed by ATRP growth of the side chains (bristles). The surface density of bottlebrushes can be precisely tailored by varying the plasmachemical deposition parameters employed for producing the poly(vinylbenzyl chloride) initiator nanolayers. Lateral force scanning probe microscopy has shown that poly(glycidyl methacrylate)-graft-poly(sodium styrene sulfonate) bottlebrush-decorated surfaces give rise to an enhancement in lubrication.

Surface actuation of smart nanoshutters.

Patterned polymer brush surfaces have been fabricated using the molecular scratchcard lithography technique, where a functional top nanolayer (acting also as a resist) is selectively removed using a scanning probe tip to expose underlying atom-transfer radical polymerization (ATRP) initiator sites. The lateral spreading of grafted polymer brush patterns across the adjacent functional resist surface can be reversibly actuated via solvent exposure. Effectively, this methodology provides a means for hiding/unveiling functional surfaces on the nanoscale.