Quantum walks: a comprehensive review

Quantum walks, the quantum mechanical counterpart of classical random walks, is an advanced tool for building quantum algorithms that has been recently shown to constitute a universal model of quantum computation. Quantum walks is now a solid field of research of quantum computation full of exciting open problems for physicists, computer scientists and engineers. In this paper we review theoretical advances on the foundations of both discrete- and continuous-time quantum walks, together with the role that randomness plays in quantum walks, the connections between the mathematical models of coined discrete quantum walks and continuous quantum walks, the quantumness of quantum walks, a summary of papers published on discrete quantum walks and entanglement as well as a succinct review of experimental proposals and realizations of discrete-time quantum walks. Furthermore, we have reviewed several algorithms based on both discrete- and continuous-time quantum walks as well as a most important result: the computational universality of both continuous- and discrete-time quantum walks.     

X-ray and electron microscopical studies of thin films of (Cd1−xZnx)S solid solution

A series of (Cd_1–x Zn _x )S powders phosphors and thin layers prepared by thermal evaporation of solid solution were studied. The phosphors used were 41% ZnS: 59% CdS with a cobalt concentration from 0 to 0.325%. The analysis of the structure of films of different thicknesses using X-ray diffraction technique confirms that the calculated relative intensities of the planes show considerable differences from the experimental results. For film thicknesses 70 nm thea axis is normal to the substrate, while at greater thicknesses (273 nm) thec axis is practically normal to the substrate. The effect of the electron beam on the solid solution indicates that layers decomposed leaving the grain boundaries decorated by metallic cadmium and zinc particles.     

AES and XPS study on the tarnishing of silver in alkaline sulphide solutions

Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) were used to follow the changes that occur on the surfaces of silver sheets when reacting with sulphide solutions of pH 12. The results obtained enabled conclusions to be drawn about the nature of the Ag₂S films. Immersion in dilute sulphide solutions ( 3 × 10^–4 M) resulted in highly irregular films that were interrupted by shallow depressions (cavities). Inside these cavities AES analysis proved the existence of massive carbon species, the presence of which delayed healing of the cavities by the formation of Ag₂S film, thus allowing the silver metal interface to continue in contact with the solution oxygen. This explains why silver electrodes maintain the Ag/Ag₂O potential while immersed in dilute sulphide solutions. Equilibration of silver with more concentrated sulphide solutions (5 × 10^–4 to 5 × 10^–3 M) effected healing of the cavities through the formation of a continuous Ag₂S film. Once this continuous film is formed, the metal interface is no longer accessible to the solution oxygen. At this point the transition of potential from Ag/Ag₂O to Ag/Ag₂S occurs.     

Autocatalytic dissolution of Pb in HNO3

The reaction between Pb and HNO₃ has been investigated using the thermometric technique. Weight-loss measurements on the reaction were also obtained. As the HNO₃ concentration is increased from 5×10^–2 to 4mol l^–1, the corrosion rate increases. This is shown thermometrically by a substantial increase in the maximum temperature attained, T _m, as well as a decrease in the time, t, required for reaching T _m. Dissolution of Pb in HNO₃ is proposed to take place according to an autocatalytic mechanism. Passivation sets were detected in solutions 11 mol l^–1 HNO₃. A parallel indication between the thermometric technique and weight-loss measurements was obtained. The rate-determining step of the autocatalytic process involves HNO₂ in dissolution of Pb in HNO₃. This is supported by the results of addition of hydrazine to the solution. This additive raises the maximum measured temperature, without affecting the corresponding time necessary to reach it. The effect of addition of NaNO₂, NaNO₃, NaCl, Na₂SO₄, NaH₂PO₄ and NaClO₄ on the reaction number, RN, of Pb in 4 mol l^–1 HNO₃ was examined. Only NaNO₂ accelerates the dissolution reaction while the other salts show as inhibition effect. It was found that these additives inhibit dissolution due to the displacement of some cathodic depolarizing components, as NO₂, from the active sites on the metal surface. The effect of addition of HCl, H₂SO₄, HClO₄ and H₃PO₄ on the reaction number, RN, of Pb in 4 mol l^–1 HNO₃ was also investigated. The observed acceleration and retardation of the dissolution of Pb was found to be dependent on both the concentration and nature of anions of the extra acids added.     

Spin singlet-triplet states of superfluid Fermi liquids in the presence of strong magnetic fields

The unitary singlet-triplet states of superfluid Fermi liquids are investigated in the presence of strong magnetic fields. The static spin susceptibility is calculated in the limith 0 in the framework of the weak coupling approximation. It is predicted that BS (a mixture of the Balian- Werthamer anisotropic state andD-wave singlet state) and 2DS (a mixture of the planar 2D state andD-wave singlet state) spin singlet-triplet states become stable at some temperatures and magnetic fields.     

Computer-Aided Search for 5-Arylideneimidazolone Anticancer Agents Able To Overcome ABCB1-Based Multidrug Resistance

ABCB1 modulation is an interesting strategy in the search for new anticancer agents that can overcome multidrug resistance (MDR). Hence, 17 new 5-arylideneimidazolones containing an amine moiety, as potential ABCB1 inhibitors, were designed, synthesized, and investigated. The series was tested in both parental (PAR) and multidrug-resistant (MDR) ABCB1-overexpressing T-lymphoma cancer cells using cytotoxicity assays. The ABCB1-modulating activity was examined in rhodamine 123 accumulation tests, followed by Pgp-Glo™ Assay to determine the influence of the most active compounds on ATPase activity. Lipophilic properties were assessed both, in silico and experimentally (RP-TLC). Pharmacophore-based molecular modelling toward ABCB1 modulation was performed. The studies allowed the identification of anticancer agents (p-fluorobenzylidene derivatives) more potent than doxorubicin, with highly selective action on MDR T-lymphoma cells (selectivity index >40). Most of the investigated compounds showed ABCB1-modulating action; in particular, two 5-benzyloxybenzylidene derivatives displayed activity nearly as strong as that of tariquidar.     

Fabrication,Electrical and Photovoltaic Characterizations of SnSb2S4/n-Si Heterojunction

Silicon - An inexpensive spray pyrolysis technique was effectively used to form a p-type SnSb2S4 thin film on n-type Si wafer for the first time to produce SnSb2S4/n-Si heterojunction. The...     

Probing the Structural and Antimicrobial Study on a Sol–Gel Derived Velosef-Loaded Bioactive Calcium Magneso-Silicate Xerogel

Silicon - The nature of the opening silicate- based surface affects the chemical interaction, spectroscopic and antimicrobial efficiency. The aim of this approach was to evaluate the spectroscopic...     

Eco-friendly Geopolymer Composite Based on Non-heat-treated Phosphate Sludge Reinforced With Polypropylene Fibers

Silicon - Geopolymers produced with metakaolin (MK) and thermally untreated phosphate sludge (PS) are beneficial and environmentally advantageous materials, but their fragility limits its...     

Modern Template Design and Biological Evaluation of Cephradine-loaded Magnesium Calcium Silicate Nanocomposites as an Inhibitor for Nosocomial Bacteria in Biomedical Applications

Silicon - Magnesium calcium silicate nanostructures (MCSNS) loaded with (0.0, 0.6, 0.9, and 1.2 wt%) of Cephradine-drug consisting of mesoporous particles were functionally prepared by sol-gel...