A Proof of the Security of Quantum Key Distribution

We prove the security of theoretical quantum key distribution against the most general attacks which can be performed on the channel, by an eavesdropper who has unlimited computation abilities, and the full power allowed by the rules of classical and quantum physics. A key created that way can then be used to transmit secure messages such that their security is also unaffected in the future.     

Nonmonotonic Coupled Dissolution-Precipitation Reactions at the Mineral–Water Interface

Dissolution is inherent to fluid-mineral systems. Yet its impact on minerals reacting with electrolytes is overlooked. Here, a novel nonmonotonic behavior for the surface interactions of carbonates (calcite and Mg-calcite) with organic acids is reported. Applying a bioinspired approach, Mg-calcite sensors via amorphous precursors, avoiding any preconditioning with functional groups are synthesized. A quartz crystal microbalance is used to study the mass changes of the mineral on contact with organic acids under varying ionic conditions, temperatures, and flow velocities. Supported by confocal Raman microscopy and potentiometric titrations, nonmonotonous mass developments are found as a function of Ca²⁺ concentration and flowrate, and attributed to three coupled chemical reactions: i) carbonate dissolution via Ca²⁺ ion complexation with organic molecules, and the formation of organo-calcium compounds as ii) a surface phase at the mineral–water interface, and iii) particles in the bulk fluid. These processes depend on local ion contents and the precipitation onset (i.e., saturation index) of organo-calcium salts, both of which substantially differ in the bulk fluid and in the fluid boundary layer at mineral interfaces. This continuum between dissolution and precipitation provides a conceptual framework to address reactions at mineral interfacial across disciplines including biomineralization, ocean acidification and reservoir geochemistry.     

Estimation of bacterial production through the coupling of (methyl 3H) Thymidine incorporation and several parameters over a Microcystis aeruginosa bloom in a hypereutrophic reservoir

The coupling of the changes in bacterial quantitative and metabolic aspects during Microcystis aeruginosa bloom conditions together with several environmental parameters was studied in the hypereutrophic Villerest reservoir, France. Bacterial abundance varied from 5.20 to 21.28 × 10⁶ bacteria-mL^?1, while bacterial biomass ranged between 75 and 507 μg C mL^?1. These results confirmed the highly eutrophic status of the Villerest reservoir. The relative quantitative importance of attached bacteria increased as Microcystis proliferated. Methyl-³H incorporation and D-(U-¹⁴C) glucose uptake varied from 8.99 to 60.57 × 10⁶ cells-mL^?1, and 0.016 to 1.587 μg CL^?1 h^?1, respectively. Correlations between several abiotic and biotic parameters showed that phytoplankton regulated bacterial growth by releasing organic carbon which is directly uptaken by heterotrophic bacteria. In the hypolimnion, the sedimentation of decaying algae represented a substantial substrate for bacterial growth.     

Simulation of the High-Frequency Response of a Heterogeneous Ground through the Finite Difference Technique

To simulate the propagation of an electromagnetic plane wave in an inhomogeneous ground, the finite difference approach can be used. One of the main problems in using this method is imposing the boundary conditions near the ground surface, especially at high frequency. Indeed, for the E polarization, the upper top of the numerical grid must be sufficiently far away from the air-ground interface in order to neglect the field due to the heterogeneities and the discretization of the atmosphere is necessary. For magneto-telluric modeling, improved boundary conditions have already been proposed. This paper deals with a new condition, valid everywhere in air and which can be applied for E and H polarization. Thus even at high frequency, as for radar applications, only one line is added to the grid discretizing the ground.     

Power system transient stability analysis: Formulation as nearly Hamiltonian systems

In this paper we formulate power systems as nonlinear nearly Hamiltonian systems. Using the invariance principle for ordinary differential equations, necessary and sufficient conditions for asymptotic stability are established and a new method of estimating the domain of attraction of the stable equilibrium point is developed. The present results constitute a novel approach to stability analysis and involve the following three steps:

1. Given a system with dissipation, the stability of its equilibrium is ascertained by determining the stability of the associated conservative system.
2. Attractivity of the stable equilibrium of the entire system (with dissipation) is determined from the system topology.
3. An estimate of the domain of attraction of the asymptotically stable equilibrium is obtained by making use of results obtained in (a) and (b).

The stability criterion developed in this paper sheds new light on the mechanism of instability in power systems and it provides analytical verification to the concept of the potential-energy boundary surface (PEBS). The PEBS is a hypersurface which makes up a part of the boundary of the domain of attraction of the stable equilibrium in a power system. The existence and properties of the PEBS have thus far been deduced primarily via simulations and heuristic methods.     

Analysis of high voltage step-up nonisolated DC–DC boost converters

A high voltage step-up nonisolated DC–DC converter based on coupled inductors suitable to photovoltaic (PV) systems applications is proposed in this paper. Considering that numerous approaches exist to extend the voltage conversion ratio of DC–DC converters that do not use transformers, a detailed comparison is also presented among the proposed converter and other popular topologies such as the conventional boost converter and the quadratic boost converter. The qualitative analysis of the coupled-inductor-based topology is developed so that a design procedure can be obtained, from which an experimental prototype is implemented to validate the theoretical assumptions.     

Rigorous optical modeling and optimization of thin‐film photovoltaic cells with textured transparent conductive oxides

Typical thin‐film photovoltaic (PV) cells incorporate a textured transparent conductive oxide to enhance light trapping and efficiently harvest solar energy. Rigorous coherent optical simulations of these devices and a complete characterization of these textured films are a challenging problem because of the several orders of magnitude difference between the wavelengths of interest and the spatial dimension of the sample that needs to be evaluated. In this paper, a practical approach for rigorous and predictive modeling of optical properties of thin‐film PV cells incorporating a vast variety of light‐trapping structures including semi‐coherent textured films and patterned coherent structures is presented. In contrast to the existing semi‐empirical device models, it is demonstrated that the presented methodology can accurately predict the scattering properties of textured fluorine‐doped tin oxide and aluminum‐doped zinc oxide conductive transparent films. It is further shown that the optical response of single‐junction and tandem‐junction PV devices incorporating such films can also be predicted with good accuracy as compared with the measured results. Next, a methodology to identify the sufficient statistical fingerprints of semi‐coherent textured films that are needed to unambiguously predict the light propagation in thin‐film cells is presented. This comprehensive approach then lends itself to identifying the optimal surface morphology needed for strong light trapping. This rigorous approach automatically includes the effects of important loss mechanisms such as the surface plasmon‐enhanced absorption in textured metal surfaces that are otherwise very difficult to account for semi‐coherent approaches based on scalar scattering theory. Copyright © 2011 John Wiley & Sons, Ltd.     

Tuning Memristivity by Varying the Oxygen Content in a Mixed Ionic–Electronic Conductor

The rising interest shown for adaptable electronics and brain‐inspired neuromorphic hardware increases the need for new device architectures and functional materials to build such devices. The rational design of these memory components also benefits the comprehension and thus the control over the microscopic mechanisms at the origin of memristivity. In oxide‐based valence‐change memories, the control of the oxygen drift and diffusion kinetics is a key aspect in obtaining the gradual analog‐type change in resistance required for artificial synapse applications. However, only a few devices are designed with this in mind, as they are commonly built around ionic insulating active materials. This shortcoming is addressed by using a mixed ionic–electronic conductor as functional memristive material. This work demonstrates how the oxygen content in La₂NiO_4+δ (L2NO4), tuned through post‐annealing treatments, has a critical influence on the memory characteristics of L2NO4‐based memristive devices. The presence of interstitial oxygen point defects in L2NO4 affects both its structure and electrical properties. High oxygen stoichiometry in the pristine state leads to an increased electrical conductivity, ultimately resulting in an improved memory window with highly multilevel, analog‐type memory programing capabilities, desirable for analog computing and synaptic applications in particular.     

Unprecedented Improvement of Single Li‐Ion Conductive Solid Polymer Electrolyte Through Salt Additive

Solid‐state lithium metal (Li°) batteries (SSLMBs) are believed to be the most promising technologies to tackle the safety concerns and the insufficient energy density encountered in conventional Li‐ion batteries. Solid polymer electrolytes (SPEs) inherently own good processability and flexibility, enabling large‐scale preparation of SSLMBs. To minimize the growth of Li° dendrites and cell polarization in SPE‐based SSLMBs, an additive‐containing single Li‐ion conductive SPE is reported. The characterization results show that a small dose of electrolyte additive (2 wt%) substantially increases the ionic conductivity of single Li‐ion conductive SPEs as well as the interfacial compatibility between electrode and SPE, allowing the cycling of SPE‐based cells with good electrochemical performance. This work may provide a paradigm shift on the design of highly cationic conductive electrolytes, which are essential for developing safe and high‐performance rechargeable batteries.