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C J Brinker

Publications and source records attributed to C J Brinker.

4 recordsLinked to original sources

Characterization of self-assembled lamellar thermoresponsive silica-hydrogel nanocomposite films.

Mesostructured lamellar nanocomposite films with alternating silica and organic layers containing poly(N-isopropropyl acrylamide) (PNIPAM) were prepared using evaporation-induced self-assembly. A suitable theoretical approach to analyze the small-angle X-ray scattering (SAXS) patterns of oriented lamellar two-phase systems was applied to the SAXS data of films of varying composition, providing details on the self-assembly process, the composition, and the polymerization. In particular, this approach allowed an accurate determination of the thickness of the silica and the organic layer. The applicability of the SAXS approach was carefully tested with simulated data and verified by thermogravimetric analysis (TGA). TGA and (13)C NMR were used to study the polymerization and linkage to the silica matrix. SAXS and time-resolved grazing incidence SAXS revealed that the phase transition of PNIPAM at ca. 32 degrees C leads to a reversible expansion/contraction perpendicular to the layers on a time scale of ca. 30 min.

Journal Article↗

Self-assembly of mesoscopically ordered chromatic polydiacetylene/silica nanocomposites.

Nature abounds with intricate composite architectures composed of hard and soft materials synergistically intertwined to provide both useful functionality and mechanical integrity. Recent synthetic efforts to mimic such natural designs have focused on nanocomposites, prepared mainly by slow procedures like monomer or polymer infiltration of inorganic nanostructures or sequential deposition. Here we report the self-assembly of conjugated polymer/silica nanocomposite films with hexagonal, cubic or lamellar mesoscopic order using polymerizable amphiphilic diacetylene molecules as both structure-directing agents and monomers. The self-assembly procedure is rapid and incorporates the organic monomers uniformly within a highly ordered, inorganic environment. Polymerization results in polydiacetylene/silica nanocomposites that are optically transparent and mechanically robust. Compared to ordered diacetylene-containing films prepared as Langmuir monolayers or by Langmuir-Blodgett deposition, the nanostructured inorganic host alters the diacetylene polymerization behaviour, and the resulting nanocomposite exhibits unusual chromatic changes in response to thermal, mechanical and chemical stimuli. The inorganic framework serves to protect, stabilize, and orient the polymer, and to mediate its function. The nanocomposite architecture also provides sufficient mechanical integrity to enable integration into devices and microsystems.

Acetylene↗

Dual SAW sensor technique for determining mass and modulus changes.

Surface acoustic wave (SAW) sensors, which are sensitive to a variety of surface changes, have been widely used for chemical and physical sensing. The ability to control or compensate for the many surface forces has been instrumental in collecting valid data. In cases in which it is not possible to neglect certain effects, such as frequency drift with temperature, methods such as the "dual sensor" technique have been utilized. This paper describes a novel use of a dual sensor technique, using two sensor materials (quartz and GaAs) to separate out the contributions of mass and modulus of the frequency change during gas adsorption experiments. The large modulus change in the film calculated using this technique and predicted by the Gassmann equation provide a greater understanding of the challenges of SAW sensing.

Journal Article↗

Optically defined multifunctional patterning of photosensitive thin-film silica mesophases.

Photosensitive films incorporating molecular photoacid generators compartmentalized within a silica-surfactant mesophase were prepared by an evaporation-induced self-assembly process. Ultraviolet exposure promoted localized acid-catalyzed siloxane condensation, which can be used for selective etching of unexposed regions; for "gray-scale" patterning of refractive index, pore size, surface area, and wetting behavior; and for optically defining a mesophase transformation (from hexagonal to tetragonal) within the film. The ability to optically define and continuously control both structure and function on the macro- and mesoscales is of interest for sensor arrays, nanoreactors, photonic and fluidic devices, and low-dielectric-constant films.

Journal Article↗