Synthesis and characterization of the new high pressure phases A Cu 3 v 4O 12 (A =Gd, Tb, Er)

New ACu3V4O12 (A=Gd, Tb, Er) phases have been prepared at high pressure and high-temperature conditions (P∼8-9 GPa, T∼1000°C) in a toroid-type high pressure cell. These compounds crystallize in the cubic symmetry with a perovskite-like structure. At ambient pressure, they are paramagnetic and have activation-type conductivity. The effect of high pressure (10-50 GPa) on the electrical properties of the materials was analyzed in the temperature range from 78 to 300 K. Pressure ranges of the transition from activation type to metallic conductivity have been determined. The crystal structure of ACu3V4O12 (A=Gd, Tb, Er) was found to be stable up to 50 GPa. © 2013 Copyright Taylor and Francis Group, LLC

Increased impedance near cut-off in plasma-like media leading to emission of high-power, narrow-bandwidth radiation

Ultra-intense, narrow-bandwidth, electromagnetic pulses have become important tools for exploring the characteristics of matter. Modern tuneable high-power light sources, such as free-electron lasers and vacuum tubes, rely on bunching of relativistic or near-relativistic electrons in vacuum. Here we present a fundamentally different method for producing narrow-bandwidth radiation from a broad spectral bandwidth current source, which takes advantage of the inflated radiation impedance close to cut-off in a medium with a plasma-like permittivity. We find that by embedding a current source in this cut-off region, more than an order of magnitude enhancement of the radiation intensity is obtained compared with emission directly into free space. The method suggests a simple and general way to flexibly use broadband current sources to produce broad or narrow bandwidth pulses. As an example, we demonstrate, using particle-in-cell simulations, enhanced monochromatic emission of terahertz radiation using a two-colour pumped current source enclosed by a tapered waveguide.ope

Electrical transport in bundled single-wall carbon nanotubes under high pressure

According to recent experimental data single wall carbon nanotubes (SWCNT) exhibit a sequence of phase transitions and demonstrate a high structural stability up to 35 GPa of non-hydrostatic pressure beyond which an irreversible transformation occurs. Here we report a study of electrical transport in SWCNTs at pressures up to 45 GPa in the temperature range of 300 - 400K. High pressure was generated in diamond anvil cell. The anvils are made of electrically conducting "carbonado"-type synthetic diamond. In the pressure range 10-25 GPa the CNT electrical resistance decreases considerably, whereas above 25 GPa it remains essentially unchanged. Such behaviour of the resistance can be connected to a structural modification of the SWCNTs accompanied by change of the conductivity character at high pressure. Raman spectra of the samples recovered after 30 GPa exhibit a large increase of D/G band intensity ratio. The Radial Breathing Mode part of the spectra remains essentially unaltered which testifies for structural integrity of the nanotubes after exposure to high non-hydrostatic pressure and lack of covalent interlinking between the tubes. Pressure dependences of resistance, activation energy for conductivity and charge carriers mobility were determined and discussed.Godkänd; 2013; 20130926 (andbra

Effect of Brønsted Acid on the Reactivity and Selectivity of the Oxoiron(V) Intermediates in C-H and C=C Oxidation Reactions

The effect of HClO4 on the reactivity and selectivity of the catalyst systems 1,2/H2O2/AcOH, based on nonheme iron complexes of the PDP families, [(Me2OMePDP)FeIII(μ-OH)2FeIII(MeOMe2PDP)](OTf)4 (1) and [(NMe2PDP)FeIII(μ-OH)2FeIII(NMe2PDP](OTf)4 (2), toward oxidation of benzylideneacetone (bna), adamantane (ada), and (3aR)-(+)-sclareolide (S) has been studied. Adding HClO4 (2–10 equiv. vs. Fe) has been found to result in the simultaneous improvement of the observed catalytic efficiency (i.e., product yields) and the oxidation regio- or enantioselectivity. At the same time, HClO4 causes a threefold increase of the second-order rate constant for the reaction of the key oxygen-transferring intermediate [(Me2OMePDP)FeV=O(OAc)]2+ (1a), with cyclohexane at −70 °C. The effect of strong Brønsted acid on the catalytic reactivity is discussed in terms of the reversible protonation of the Fe=O moiety of the parent perferryl intermediates