The ability to control the surface composition and morphology of alloy catalysts is critical for achieving high activity and durability of catalysts for oxygen reduction reaction (ORR) and fuel cells. This report describes an efficient surfactant-free synthesis route for producing a twisty nanowire (TNW) shaped platinum−iron (PtFe) alloy catalyst (denoted as PtFe TNWs) with controllable bimetallic compositions. PtFe TNWs with an optimal initial composition of ∼24% Pt are shown to exhibit the highest mass activity (3.4 A/mg Pt , ∼20 times higher than that of commercial Pt catalyst) and the highest durability (<2% loss of activity after 40 000 cycles and <30% loss after 120 000 cycles) among all PtFe-based nanocatalysts under ORR or fuel cell operating conditions reported so far. Using ex situ and in situ synchrotron X-ray diffraction coupled with atomic pair distribution function (PDF) analysis and 3D modeling, the PtFe TNWs are shown to exhibit mixed face-centered cubic (fcc)−body-centered cubic (bcc) alloy structure and a significant lattice strain. A striking finding is that the activity strongly depends on the composition of the as-synthesized catalysts and this dependence remains unchanged despite the evolution of the composition of the different catalysts and their lattice constants under ORR or fuel cell operating conditions. Notably, dealloying under fuel cell operating condition starts at phase-segregated domain sites leading to a final fcc alloy structure with subtle differences in surface morphology. Due to a subsequent realloying and the morphology of TNWs, the surface lattice strain observed with the as-synthesized catalysts is largely preserved. This strain and the particular facets exhibited by the TNWs are believed to be responsible for the observed activity and durability enhancements. These findings provide new insights into the correlation between the structure, activity, and durability of nanoalloy catalysts and are expected to energize the ongoing effort to develop highly active and durable low-Pt-content nanowire catalysts by controlling their alloy structure and morphology.

A virtual source that yields a family of a Pearcey wave is demonstrated. A closed-form expression is derived for the Pearcey wave that simplifies to the paraxial Pearcey beam (PB) in the appropriate limit. From the perturbative series representation of a complex-source-point spherical wave, an infinite series nonparaxial correction expression for a PB is obtained. The infinite series expression of a PB can give accuracy up to any order of the diffraction angle. By applying the integral representation of the Pearcey wave, the first three terms in the nonparaxial correction series to the paraxial PB are provided.

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Capillary zone electrophoresis was employed to the analysis of adenine and guanine by using end-column amperometric detector with a carbon fiber microdisk array electrode. Optimum conditions of separation and detection are 0.01 moln H3P04-0.01 mom H3B03-0.01 mom HAc-NaOH (pH 9.2) for the buffer solution, 20 kV for the separation voltage, 3.0kV and 5 s for injection voltage and time, respectively, and 1.00 V (vs.SCE) for the detection potential. The limit of detection is 8.2 fmol for adenine and 2.9 fmol for guanine (S1N = 2). The method was applied to determination of adenine and guanine in hydrolytic product of yeast-RNA and calf thymus-DNA.