A study on the oxygen reduction reaction ͑ORR͒ mechanism that occurs on non-platinum electrocatalysts, specifically materials derived from pyrolyzed cobalt tetramethoxyphenyl porphyrin in acidic media, is presented here. Reactant and product flux analysis is performed on rotating ring-disk electrode ͑RRDE͒ data to evaluate the non-platinum-based materials. An in-depth X-ray photelectron spectroscopy surface characterization analysis is performed and discussed in the context of structure-to-property correlations that are established using a multivariant analysis technique. Pyrolyzed cobalt porphyrin catalysts are highly heterogeneous materials that include both Co species that are associated with nitrogen ͑CoN x ͒ and Co nanoparticles coated by "native" Co oxides. This study proposes an ORR mechanism that occurs on this class of non-Pt electrocatalysts based on structure-toproperty correlations and qualitative analysis of the RRDE flux data. The combined flux analysis and structural characterization suggests that the series type, 2 ϫ 2 peroxide ORR pathway is supported on the bifunctional catalyst materials. In this model, two distinct active sites are involved following a bifunctional catalysis scheme. It is suggested that oxygen is initially adsorbed and reduced to peroxide on a CoN x -type site. The intermediate product, peroxide, can be further reduced to water in a series reaction step on a decorating active cobalt oxide species on the catalyst surface.

A series of water soluble, cationic conjugated polyelectrolytes (CPEs) with backbones based on a poly(phenylene ethynylene) repeat unit structure and tetraakylammonium side groups exhibit a profound light-induced biocidal effect. The present study examines the biocidal activity of the CPEs, correlating this activity with the photophysical properties of the polymers. The photophysical properties of the CPEs are studied in solution, and the results demonstrate that direct excitation produces a triplet excited-state in moderate yield, and the triplet is shown to be effective at sensitizing the production of singlet oxygen. Using the polymers in a format where they are physisorbed or covalently grafted to the surface of colloidal silica particles (5 and 30 microm diameter), we demonstrate that they exhibit light-activated biocidal activity, effectively killing Cobetia marina and Pseudomonas aeruginosa. The light-induced biocidal activity is also correlated with a requirement for oxygen suggesting that interfacial generation of singlet oxygen is the crucial step in the light-induced biocidal activity.

We describe a facile method for the formation of dynamic nanostructured surfaces based on the modification of porous anodic aluminum oxide with poly(N-isopropyl acrylamide) (PNIPAAm) via surface-initiated atom transfer radical polymerization. The dynamic structure of these surfaces was investigated by atomic force microscopy (AFM), which showed dramatic changes in the surface nanostructure above and below the aqueous lower critical solution temperature of PNIPAAm. These changes in surface structure are correlated with changes in the macroscopic wettability of the surfaces, which was probed by water contact angle measurements. Principal component analysis was used to develop a quantitative correlation between AFM image intensity histograms and macroscopic wettability. Such correlations and dynamic nanostructured surfaces may have a variety of uses.

The chemical structure of non-platinum electrocatalysts obtained from cobalt porphyrins (CoTMPP or CoTPP) by pyrolysis is investigated by X-ray Photoelectron Spectroscopy (XPS). The catalysts represent highly dispersed, self-supported nano-composites that demonstrate electrocatalytic performance for oxygen reduction and practically no activity in methanol electro-oxidation. High-resolution Co2p, C1s, N1s and O1s XPS spectra acquired from precursors and electrocatalysts pyrolyzed at various experimental conditions were curve-fit using (a) individual peaks of constrained width and shape as well as (b) experimentally obtained photopeaks from the precursor with additional peaks required for a complete curve fit. Principal Component Analysis (PCA) applied to quantitative results from the curve-fits of both types of spectra facilitates visualization and identification of the chemical species that are formed or destroyed, and simplifies evaluation of critical correlations. As a result of these studies it is established that the catalyst is a nano-composite of highly dispersed pyropolymer with some remaining N x -centers inserted into a graphite-like matrix. Approximately 50% of the metal is distributed as Co 2+ , associated with N 4 -centers. The remaining cobalt is present in crystallites of metallic Co. A thin layer of CoO coats these metallic cobalt phases. The developed methodology, described herein, combines model curve-fits and principal component analysis (PCA), resulting in a quantitative and unambiguous understanding of the chemical composition and structure of complex electrocatalysts.