We have prepared and analyzed thin film structures formed by polyethylenimine and alkyltrimethylammonium bromide (C n TAB) surfactants at the air/water interface, using both surface and bulk sensitive techniques. In initial experiments it was observed that hexagonal arrays of rodlike micelles surrounded by the polymer were formed at the solution surface, with the principal axis of the micelles running parallel to the surface. In the studies reported here, the formation of these ordered mesostructured films was identified as being kinetically but not thermodynamically favored, with some of the systems examined showing a loss of structure from their neutron reflectometry profiles with time. The polymer was used in both an as-diluted state (with a small net positive charge) and a neutral state, through the addition of sodium hydroxide to the solution. The primary interaction in these systems was found to be that of a neutral polymer with a cationic surfactant; however, by modifying the charge on the polymer it is possible to alter the distance between micelles by up to 6 Å without destroying the structure of the films. Analysis of the bulk solution with small-angle neutron scattering showed that the micelles in solution are elliptical rather than rod-shaped, and so the assembly of the hexagonal mesostructure occurs at the air/water interface rather than adsorbing to the interface from the bulk.

No abstract

No abstract

No abstract

Thin films of TiO2 (anatase) nanoparticles are assembled at an electrode surface via a layer-by-layer deposition process employing phytic acid, pyromellitic acid, or flavin adenine dinucleotide (FAD) as molecular binders. With all three types of binders, layers of typically 30 nm thickness are formed each deposition cycle. FAD as an electrochemically active component immobilized at the surface of the TiO2 particles is reduced to FADH2 and reoxidized in a chemically reversible two electron-two proton redox process. Two distinct voltammetric signals are observed for the immobilized FAD redox system associated with (i) hopping of electrons at the TiO2 surface (reversible) and (ii) conduction of electrons through the TiO2 assembly (irreversible). The conduction of electrons through the TiO2 assembly is possible by diffusion over considerable distances as well as through a "spacer" layer of TiO2 phytate. An order of magnitude (upper limit) estimate for the diffusion coefficient of electrons through TiO2 phytate, D(electron) approximately 10(-6) m(2) s(-1), is obtained from voltammetric data. Finally, it is demonstrated that the calcination of TiO2 assemblies causes dramatic changes in the electron transfer kinetics for the immobilized FAD/FADH2 redox system.