Theory of carrier concentration-dependent electronic behavior in layered cobaltates

A natural explanation for the carrier concentration-dependent electronic behavior in the layered cobaltates emerges within correlated-electron Hamiltonians with finite on-site and significant nearest neighbor hole-hole Coulomb repulsions. The nearest neighbor repulsion decreases hole double occupancy below hole density 1/3, but increases the same at higher hole densities. Our conclusion is valid for both single-band and three-band extended Hubbard Hamiltonians, and sheds light on concentration dependent e'(g) hole occupancy within the latter.     

Metal ion-induced H-aggregation of a water-soluble anionic dye Congo red (CR) in Langmuir–Blodgett (LB) film

Present communication reports the preparation of Langmuir monolayer of water-soluble anionic dye Congo red (CR) by allowing it to adsorb from the aqueous subphase onto the preformed Langmuir monolayer of anionic stearic acid using divalent metal cations Mg²⁺ as mediator. Isotherm and compressibility studies of SA-Mg-CR hybrid monolayer gave valuable information about the molecular organisation in the Langmuir monolayer. Absorption spectroscopic studies revealed the formation of H-aggregates in the hybrid Langmuir–Blodgett (LB) films fabricated at lower salt concentration in the subphase. Atomic Force Microscopic image gave visual evidence of distinct nanocrystalline domains in the LB monolayer film.     

Redefining the transparency order

In this paper, we consider the multi-bit Differential Power Analysis (DPA) in the Hamming weight model. In this regard, we revisit the definition of Transparency Order (\(\mathsf {TO}\)) from the work of Prouff (FSE 2005) and find that the definition has certain limitations. Although this work has been quite well referred in the literature, surprisingly, these limitations remained unexplored for almost a decade. We analyse the definition from scratch, modify it and finally provide a definition with better insight that can theoretically capture DPA in Hamming weight model for hardware implementation with precharge logic. At the end, we confront the notion of (revised) transparency order with attack simulations in order to study to what extent the low transparency order of an s-box impacts the efficiency of a side channel attack against its processing. To the best of our knowledge, this is the first time that such a critical analysis is conducted (even considering the original notion of Prouff). It practically confirms that the transparency order is indeed related to the resistance of the s-box against side-channel attacks, but it also shows that it is not sufficient alone to directly achieve a satisfying level of security. Regarding this point, our conclusion is that the (revised) transparency order is a valuable criterion to consider when designing a cryptographic algorithm, and even if it does not preclude to also use classical countermeasures like masking or shuffling, it enables to improve their effectiveness.     

Colloidal synthesis of magnetic CuCr2S4 nanocrystals and nanoclusters

Nanocrystals and nanoclusters of the room-temperature magnetic spinel CuCr(2)S(4) have been synthesized using a facile solution-based method. The synthesis involves hot injection of an excess of 1-dodecanethiol (1-DDT) into a boiling coordinating solvent containing CuCl(2) and CrCl(3)·6H(2)O. Using octadecylamine (ODA) as a solvent yields cube-shaped nanocrystals with an average size of 20 ± 2 nm, while with oleylamine (OLA), nanoclusters with an average size of 31 ± 2.5 nm are obtained. In both cases, powder X-ray diffraction patterns confirmed the formation of the pure spinel phase without any impurities. While the synthesized powders are superparamagnetic near room temperature, they exhibit ferromagnetic behavior at lower temperatures, with magnetization (M(S)) values of 30 emu/g (1.63 μ(B)/f.u.) and 33 emu/g (1.79 μ(B)/f.u.) for the ODA- and OLA-capped nanocrystals and nanoclusters, respectively, at 5 K.     

Thermodynamics of water entry in hydrophobic channels of carbon nanotubes

Experiments and computer simulations demonstrate that water spontaneously fills the hydrophobic cavity of a carbon nanotube. To gain a quantitative thermodynamic understanding of this phenomenon, we use the recently developed two phase thermodynamics method to compute translational and rotational entropies of confined water molecules inside single-walled carbon nanotubes and show that the increase in energy of a water molecule inside the nanotube is compensated by the gain in its rotational entropy. The confined water is in equilibrium with the bulk water and the Helmholtz free energy per water molecule of confined water is the same as that in the bulk within the accuracy of the simulation results. A comparison of translational and rotational spectra of water molecules confined in carbon nanotubes with that of bulk water shows significant shifts in the positions of the spectral peaks that are directly related to the tube radius.     

Summary of the CMS potential for the Higgs boson discovery

The European Physical Journal C - This work summarizes the studies for the Higgs boson searches in CMS at the LHC collider. The main discovery channels are presented and the potential is given for...