Photocatalytic hydrogen evolution over semiconducting niobate nanosheets is synergistically improved by coexisting photochemically inactive additives of clay particles and sodium chloride without precise nanoscopic structural regulation. In addition, the Pt cocatalyst loaded on the clay particles works better than that photodeposited on the photocatalytic nanosheets.

The impregnation method was used to synthesize Pt and Pt3Co supported on MWCNTs applying NaBH4 as the reducing agent. The structure, morphology, and chemical composition of the electrocatalysts were characterized through SEM, XRD, and EDX. X-ray diffraction showed a good crystallinity of the supported Pt nanoparticles on the composites and showed the formation of Pt3<...

A soluble Pt nanocluster catalyst (Pt-GLY) is efficient in the absence of base for aqueous-phase aerobic oxidation of, in particular, non-activated alcohols with high recyclability.

In paper I [M. Znojil and G. Lévai, Phys. Lett. A 271 (2000) 327] we introduced the Coulomb Kratzer bound-state problem in its cryptohermitian, PT −symmetric version. An instability of the original model is revealed here. A necessary stabilization is achieved, for almost all couplings, by an unusual, negative choice of the bare mass in Schrödiner equation.

We discuss several PT -symmetric deformations of superderivatives. Based on these various possibilities, we propose new families of complex PT -symmetric deformations of the supersymmetric Korteweg-de Vries equation. Some of these new models are mere fermionic extensions of the former in the sense that they are formulated in terms of superspace valued superfields containing bosonic and fermioni...

The electrocatalysis of the oxygen reduction reaction (ORR) on carbon supportedPt-V (1:1) catalyst in polymer electrolyte fuel cells (PEFC) was investigated. Atan oxygen pressure of one atm an enhanced electrocatalytic property of Pt-V/Ccompared with Pt/C is revealed. These results indicate the occurrence of adifferent electrocatalytic mechanism for the ORR on Pt/C and Pt-V/C. Anincrease of mas...

Chemical properties of epitaxially grown bimetallic layers may deviate substantially from the behavior of their constituents. Strain in conjunction with electronic effects due to the nearby interface represent the dominant contribution to this modification. One of the simplest surface processes to characterize reactivity of these substrates is the dissociative adsorption of an incoming homo-nuc...