Nine non-noble-metal catalysts (NNMCs) from five different laboratories were investigated for the catalysis of O(2) electroreduction in an acidic medium. The catalyst precursors were synthesized by wet impregnation, planetary ball milling, a foaming-agent technique, or a templating method. All catalyst precursors were subjected to one or more heat treatments at 700-1050 degrees C in an inert or reactive atmosphere. These catalysts underwent an identical set of electrochemical characterizations, including rotating-disk-electrode and polymer-electrolyte membrane fuel cell (PEMFC) tests and voltammetry under N(2). Ex situ characterization was comprised of X-ray photoelectron spectroscopy, neutron activation analysis, scanning electron microscopy, and N(2) adsorption and its analysis with an advanced model for carbonaceous powders. In PEMFC, several NNMCs display mass activities of 10-20 A g(-1) at 0.8 V versus a reversible hydrogen electrode, and one shows 80 A g(-1). The latter value corresponds to a volumetric activity of 19 A cm(-3) under reference conditions and represents one-seventh of the target defined by the U.S. Department of Energy for 2010 (130 A cm(-3)). The activity of all NNMCs is mainly governed by the microporous surface area, and active sites seem to be hosted in pore sizes of 5-15 A. The nitrogen and metal (iron or cobalt) seem to be present in sufficient amounts in the NNMCs and do not limit activity. The paper discusses probable directions for synthesizing more active NNMCs. This could be achieved through multiple pyrolysis steps, ball-milling steps, and control of the powder morphology by the addition of foaming agents and/or sulfur.

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A low-temperature bonding process to form joints with high strength and ionic migration resistance using mixed Cu-Ag nanoparticles was studied. Although it was difficult to obtain strong joints using Cu nanoparticles, with the addition of Ag nanoparticles to the Cu nanoparticles the bonding strength of the Cu-to-Cu joints increased. The joints formed by the mixed Cu-Ag nanoparticles at 350°C exhibited a high bonding strength of $50 MPa. Counterelectrodes made of the mixed Cu-Ag nanoparticles had four times higher ionic migration resistance compared with counterelectrodes made only of Ag nanoparticles.

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Radiocesium ((134)Cs + (137)Cs) deposition from the Fukushima nuclear power plant accident was measured in 20 woody plants (12 evergreen and 8 deciduous species) grown in Abiko (approximately 200 km SSW from the NPP). Leaves (needles) and twigs were sampled from each of three foliar positions (top, middle, and bottom) in the plant canopy in early August 2011. At the time, soils around the plants were also sampled, and gamma radiation dose rates were measured at each sampling position. The average radiocesium activity in the observed leaves of the evergreen species was 7.7 times that in the leaves of the deciduous species. Among the observed evergreen coniferous species, the activity in pre-fallout-expanded leaves was 2.4 times that in the post-fallout-expanded leaves. Notably, a distinct variation in the activity among the evergreen coniferous species could be observed for the post-fallout-expanded leaves but not for the pre-fallout-expanded leaves. Although these differences depend on whether the leaves had expanded at the time of the fallout, it is probable that a considerable amount of radiocesium was translocated to newly developed leaves at a species-specific rate. In addition, it was demonstrated that dose rates around woody plants were not consistent with the prevailing prediction that general dose rates correspondingly decrease with monitoring height from the ground. Thus, the dose rates in the top foliar layer of the deciduous species decreased more than predicted, whereas those in the top foliar layer of the coniferous species did not decrease. This may be due to differences in the balance between the attenuation resulting from a shielding effect of the plant bodies and the higher radiocesium accumulation in the leaves.