Ni–Fe and Ni–Fe–Co mixed-metal oxide (MMO) films were investigated as electrocatalysts for the oxygen evolution reaction (OER) in 0.1 M KOH. In an effort to optimize MMO morphology, aniline was used as a capping agent to produce high-surface-area Ni–Fe–Co films on Raney nickel supports. This catalyst exhibits enhanced mass activity in comparison to the Ni–Fe OER electrocatalysts reported to date. Cyclic voltammetry shows changes in the potential of the Ni2+/3+ transitions in Fe- or Co-containing MMO films. In situ X-ray absorption spectroscopy (XAS) analysis confirms that Fe acts to stabilize Ni in the 2+ oxidation state, while Co facilitates oxidation to the 3+ state. The results of this study support the recent claims that Fe (not Ni) is the OER active site. The OER enhancement of the ternary Ni–Fe–Co catalyst results from two effects: (1) the charge-transfer effects of Co result in the formation of the conductive NiIIIOOH phase at lower overpotential, thus activating the Fe sites which are otherwise inaccessible to electron transfer in the nonconductive NiII(OH)2 host lattice, and (2) XAS analysis shows that the presence of Co effectively “shrinks” the Ni and Fe local geometry, likely resulting in an optimized Fe–OH/OOH bond strength. In addition, analysis of heat-treatment effects indicates that calcination at 400 °C improves the OER activity of Ni–Fe–Co but deactivates Ni–Fe. Annealing studies under argon show that MMO surfaces with a hydrated Ni­(OH)2 phase and a crystalline NiO phase exhibit nearly identical OER activities. Finally, the morphology of the MMO catalyst film on Raney Ni support provides excellent catalyst dispersion and should result in high active-site utilization for use in technologically relevant gas-diffusion electrodes.

Despite the fundamental and practical significance of the hydrogen evolution and oxidation reactions (HER/HOR), their kinetics in base remain unclear. Herein, we show that the alkaline HER/HOR kinetics can be unified by the catalytic roles of the adsorbed hydroxyl (OHad)-water-alkali metal cation (AM+) adducts, on the basis of the observations that enriching the OHad abundance via surface Ni benefits the HER/HOR; increasing the AM+ concentration only promotes the HER, while varying the identity of AM+ affects both HER/HOR. The presence of OHad-(H2O) x -AM+ in the double-layer region facilitates the OHad removal into the bulk, forming OH–-(H2O) x -AM+ as per the hard–soft acid–base theory, thereby selectively promoting the HER. It can be detrimental to the HOR as per the bifunctional mechanism, as the AM+ destabilizes the OHad, which is further supported by the CO oxidation results. This new notion may be important for alkaline electrochemistry.

We report an interesting new class of bifunctional electrocatalysts, Pd/C-CeO2, with excellent activity and stability for the hydrogen oxidation reaction (HOR) under alkaline conditions. The unique structure of palladium deposited onto a mixed support of Vulcan XC-72 carbon and CeO2 consists of Pd metal preferable deposited on the ceria regions of the catalyst. The CeO2-Pd interaction leads to enhanced HOR kinetics and increased stability. Here we compare catalysts with three different Pd loadings and show that the 10 wt% Pd sample has optimized activity. Hydrogen pumping and fuel cell experiments based on this catalyst show higher activities as compared to a Pd/C sample without ceria. Metal dissolution tests and identical location transmission microscopy experiments show that the catalyst stability under harsh potential cycling experiments in alkaline medium is significantly improved as compared to Pd/C, making this material one of the best options for use as highly active and highly stable electrocatalysts for the HOR in anion exchange membrane fuel cells

Theranostics, which is the combination of both therapeutic and diagnostic capacities in one dose, is a promising tool for both clinical application and research. Although there are many chromophores available for optical imaging, their applications are limited due to the photobleaching property or intrinsic toxicity. Curcumin, a natural compound extracted from the rhizome of curcuma longa, is well known thanks to its bio-pharmaceutical activities and strong fluorescence as biocompatible probe for bio-imaging. In this study, we aimed to fabricate a system with dual functions: diagnostic and therapeutic, based on poly(lactide)-tocopheryl polyethylene glycol succinate (PLA-TPGS) micelles co-loaded curcumin (Cur) and paclitaxel (PTX). Two kinds of curcumin nanoparticle (NP) were fabricated and characterized by Fourier transform infrared spectroscopy, field emission scanning electron microscopy and dynamic light scattering methods. The cellular uptake and fluorescent activities of curcumin in these systems were also tested by bioassay studies, and were compared with paclitaxe-oregon. The results showed that (Cur + PTX)-PLA-TPGS NPs is a potential system for cancer theranostics.

No abstract