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The effect of 1,3-dioxolane (DOL) based electrolyte solutions (DOL/LiTFSI and DOL/LiTFSI-LiNO(3)) on the electrochemical performance and surface chemistry of silicon nanowire (SiNW) anodes was systematically investigated. SiNWs exhibited an exceptional electrochemical performance in DOL solutions in contrast to standard alkyl carbonate solutions (EC-DMC/LiPF(6)). Reduced irreversible capacity losses, enhanced and stable reversible capacities over prolonged cycling, and lower impedance were identified with DOL solutions. After 1000 charge-discharge cycles (at 60 °C and a 6 C rate), SiNWs in DOL/LiTFSI-LiNO(3) solution exhibited a reversible capacity of 1275 mAh/g, whereas only 575 and 20 mAh/g were identified in DOL/LiTFSI and EC-DMC solutions, respectively. Transmission electron microscopy (TEM) studies demonstrated the complete and uniform lithiation of SiNWs in DOL-based electrolyte solutions and incomplete, nonuniform lithiation in EC-DMC solutions. In addition, the formation of compact and uniform surface films on SiNWs cycled in DOL-based electrolyte solutions was identified by scanning electron microscopic (SEM) imaging, while the surface films formed in EC-DMC based solutions were thick and nonuniform. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) spectroscopy were employed to analyze the surface chemistry of SiNWs cycled in EC-DMC and DOL based electrolyte solutions. The distinctive surface chemistry of SiNWs cycled in DOL based electrolyte solutions was found to be responsible for their enhanced electrochemical performances., (© 2012 American Chemical Society)

The effect of FEC as a co-solvent on the electrochemical performance and surface chemistry of silicon nanowire (SiNW) anodes was thoroughly investigated. Enhanced electrochemical performance was observed for SiNW anodes in alkyl carbonates electrolyte solutions containing fluoroethylene carbonate (FEC). Reduced irreversible capacity losses accompanied by enhanced and stable reversible capacities over prolonged cycling were achieved with FEC-containing electrolyte solutions. TEM studies provided evidence for the complete and incomplete lithiation of SiNW's in FEC-containing and FEC-free electrolyte solutions, respectively. Scanning electron microscopy (SEM) results proved the formation of much thinner and compact surface films on SiNW's in FEC-containing solutions. However, thicker surface films were identified for SiNW electrodes cycled in FEC-free solutions. SiNW electrodes develop lower impedance in electrolyte solutions containing FEC in contrast to standard (FEC-free) solutions. The surface chemistry of SiNW electrodes cycled in FEC-modified and standard electrolytes were investigated using X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) spectroscopy. The impact of FEC as a co-solvent on the electrochemical behavior of SiNW electrodes is discussed herein in light of the spectroscopic and microscopic studies.

A new model of quartz-crystal impedance (QCI) of nonuniform layers composed of bumps of carbon particles (either porous or nonporous) and a polymeric binder layer has been proposed. The solid particles are modeled by semispherical and oblate semispheroid bumps embedded into the "sea" of a polymeric binder layer. On the basis of this model and elaborating on the principles of hydrodynamic spectroscopy of composite electrode materials, the geometric and porous structure parameters of nanoporous carbon and nonporous graphite composite electrodes in contact with liquids have been reliably determined. This work is believed to create a solid theoretical background for both advanced studies and optimized formulations of the composite electrodes suited to practical electrochemical devices and for the interpretation of the processes of ions and solvent insertion into nanoporous carbon electrodes uniquely probed by the QCI method (supercapacitive cells, desalination membranes).

A route for the preparation of binder-free sulfur-carbon cathodes is developed for lithium sulfur batteries. The method is based on the impregnation of elemental sulfur into the micropores of activated carbon fibers. These electrodes demonstrate good electrochemical performance at high current density attributed to the uniform dispersion of sulfur inside the carbon fiber., (Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

We present a rigorous analysis of unique, wide electrochemical window solutions for rechargeable magnesium batteries, based on aromatic ligands containing organometallic complexes. These solutions are comprised of the transmetalation reaction products of Ph(x)MgCl(2-x) and Ph(y)AlCl(3-y) in different proportions, in THF. In principle, these reactions involve the exchange of ligands between the magnesium and the aluminum based compounds, forming ionic species and neutral molecules, such as Mg(2)Cl(3)(+)·6THF, MgCl(2)·4THF, and Ph(y)AlCl(4-y)(-) (y = 0-4). The identification of the equilibrium species in the solutions is carried out by a combination of Raman spectroscopy, multinuclear NMR, and single-crystal XRD analyses. The association of the spectroscopic results with explicit identifiable species is supported by spectral analyses of specially synthesized reference compounds and DFT quantum-mechanical calculations. The correlation between the identified solution equilibrium species and the electrochemical anodic stability window is investigated. This study advances both development of new nonaqueous solution chemistry and possible development of high-energy density rechargeable Mg batteries.

Combined application of cyclic voltammetry (CV) and electrochemical quartz crystal microbalance (EQCM) technique reveals a complicated interplay between the adsorption of ammonium and lower molecular weight tetraalkyl ammonium cations and desorption of Cl(-) anions inside carbon micropores at low surface charge densities, which results in failure of their permselectivity. Higher negative surface charge densities induce complete exclusion (desorption) of the Cl(-) co-ions, which imparts purely permselective behavior on the carbon micropores. The second fundamental effect discovered herein relates to the dominant role of anion desorption (as compared to cation adsorption), that is, overwhelming failure of permselectivity extends to high negative charge densities of the electrode in the presence of bulky tetraalkyl ammonium cations, which tend to be confined in the micropores of the carbon. The results obtained are important for advancement of high power density carbon-based supercapacitors, nanofiltration technologies with porous carbon membranes, and studies of ionic transport across biological membranes., (Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

We propose herein a new reliable approach to assess solvation numbers of ions confined in carbon nanopores based on dynamic quartz crystal measurements. This was proved for the entire families of alkaline, alkaline-earth cations, and halogen anions. As-assessed hydration numbers appear in the sequence characteristic of a transition from the cosmotropic to a chaotropic-type behavior with the decrease of the ion's charge-to-size ratio. The information on the behavior of ions confined in nanometric space of different (especially charged) carbon materials is in high demand for the development of powerful supercapacitors, nanofiltration membranes, and chemical/biochemical sensors.

Electrochemical quartz crystal microbalance (EQCM) technique provides a direct assessment to the behavior of electroadsorbed ions and solvent molecules confined in micropores of activated carbon electrodes in contact with practically important aprotic electrolyte solutions. The estimated value of the solvation number equal to 3 is evident for a partial desolvation of Li(+) cations when adsorbed in carbon micropores.

Large-scale self-organization occurring on the scale of dozens of micrometers in rapidly evaporated polymer solutions based on amorphous polymers and chlorinated solvents was studied. Heating the substrate from below destroys the patterning. This contradicts the idea that self-organization is due to the jump in surface tension caused by a temperature gradient (temperature-gradient-driven Marangoni instability). We relate the patterning to the concentration-gradient- driven effects., (2009 Elsevier Inc. All rights reserved.)

Chevrel phases (CPs), M(x)Mo(6)T(8) (M = metal, T = S, Se) are unique materials, which allow for a fast and reversible insertion of various cations at room temperature. In spite of extensive studies of these materials, the origin of their high ionic mobility remained unclear. In a previous paper we presented for the first time a proper classification of the very complex transport behavior of different cations in the Mo(6)T(8) hosts: (i) apparent immobility of the large M cations such as Pb(2+), Sn(2+), Ag(+) in the ternary phases, MMo(6)T(8); (ii) coupled M+M' diffusion in the quaternary phases, M(x)M'(y)Mo(6)T(8), where both large and small cations can assist; (iii) cation trapping in the Mg-Mo(6)S(8), Cd-Mo(6)S(8), and Na-Mo(6)T(8) systems; (iv) a combination of low- and high-rate diffusion kinetics at the first and last intercalation stages, respectively, for the Cu-Mo(6)S(8), Mn-Mo(6)S(8), and Cd-Mo(6)Se(8) systems, and (v) a fast ionic transport for small cations such as Ni(2+), Zn(2+), and Li(+). It was shown that this behavior could be understood by a relatively simple crystallographic analysis (mapping of all the cation sites and estimations of their potential energy according to the distances of these sites from adjacent anions and cations) of the diffusion routes, which differ for different cations. For this analysis, it was necessary to complete our knowledge about the cation location in the crystal structure for several CPs with known ionic mobility. This article presents the results of a combined Rietveld analysis of powder X-ray and high-resolution neutron diffraction profiles for NaMo(6)T(8), ZnMo(6)T(8), CdMo(6)T(8), and MnMo(6)S(8). All seven compounds can be defined as classic CPs, where cation delocalization from the center of the largest cavity between the Mo(6)T(8) blocks decreases with the length of the ideal chemical bond, M-T. In addition, this work details the effect of the structural parameters on the ionic conductivity in CPs, namely, it shows how subtle changes in cation delocalization may be crucial for diffusion kinetics.

Wetting transitions were studied with vertically-vibrated drops on various artificial and natural rough substrates. Alternative pathways of wetting transitions were observed. The model of wetting transition is presented. Multiple minima of the Gibbs free energy of a drop deposited on a rough surface explain alternative pathways of wetting transitions. We demonstrate that a wetting transition occurs when the constant force resulting from vibrations, Laplace and hydrostatic pressure acts on the triple line. It is shown that the final wetting states are mainly the Cassie impregnating wetting state with water penetrating the pores in the outer vicinity of the droplet or the Wenzel state with water inside the pores under the droplet whereas the substrate ahead the drop is dry.

Water contact angles on polysulfone and polyethersulfone films exposed to UV irradiation have been found to decrease dramatically. We relate this phenomenon to the formation and release of disulfonic acid from the irradiated films, a well-known surfactant. The phenomenon appears to be reversible, namely, cleansed surfaces retained their initial contact angle. The revealed phenomenon may provide a means of controlling the spreading of liquids on polysulfone and polyethersulfone films and seems promising for use in microfluidics applications.

This series of papers is devoted to unique cathode materials for Mg batteries, MgxMo6T8 (T = S, Se, x = 1 and 2) Chevrel phases (CPs). In this part, a combination of neutron and high-resolution synchrotron X-ray diffractions was used to study the crystal structure of Mg2Mo6Se8, which is triclinic at room temperature (space group P1, a = 6.868 A, b = 6.921 A, c = 6.880 A, alpha = 93.00 degrees , beta = 94.40 degrees , gamma = 96.22 degrees ). In contrast to other members of the MgxMo6T8 family, this compound does not follow the classic scheme of successive cation insertion into so-called inner and outer sites: Both the Mg(2+) ions per formula are located in the tetrahedral sites of the outer ring. This surprising cation location, predicted previously for Mg-containing CPs by ab initio calculations, provides the uniform distribution of the cation charge in the triclinic structure, which is similar to that of rhombohedral CPs. A mapping of the cation sites was widely used to demonstrate the variety of cation arrangement in CPs and the factors affecting this arrangement, as well as to clarify the origin of the exceptionally high mobility of the Mg(2+) ions in Mg2Mo6Se8.

Combined CV studies and UV-Vis-NIR spectroelectrochemical investigations revealed an unusual stability of the p- and n-doped PMOThOD in the wide potential window of 4 V. The n-doping process occurs in this polymer down to -2.7 V (vs. Ag/Ag+) in a non-destructive way with the characteristic development of the omega3 transition as a function of the doping level. In situ electronic transport studies revealed a high conductivity of the n-doped polymer which implies high mobility of the negatively charged carriers in the freshly doped PMOThOD film electrodes. An increase in the cathodic polarization, long-term cycling of the film electrodes, especially of higher thickness, results in a growing contribution of the negatively charged carriers trapping to the redox properties of the PMOThOD. The trapping of the charged carriers reduces gradually the electronic conductance of the PMOThOD film, but its effect on the redox-capacity of the film (in a typical scan rates range up to 50 mV s(-1)) is only minor.

In this paper, we report on attempts to use differential scanning calorimetric measurements of aged Li electrodes for the study of the kinetics of the growth of surface films on the active metal. Standard, commonly used alkyl carbonate solutions such as ethylene and di-methyl carbonates with LiPF6 were explored. Heating Li samples in solutions after aging by DSC, resulted in well-resolved curves of reaction heats vs temperature. Exothermic reactions occurring at temperatures below 150 degrees C could be attributed to changes related to the surface films and their heat evolved, increased as a function of storage time, and hence these heats represent the thickness of the surface films that grow upon storage. Scanning electron microscopy of the Li surfaces as a function of storage and heating to different temperatures confirmed that the thermal reactions of Li surfaces in these solutions up to 150 degrees C relate to the surface films only. XPS studies revealed that these processes of the surface films change the metastable organic Li salts to more stable inorganic compounds such as LiF and Li2O. Massive red-ox reactions, between the salt anion and the solvents and between the solution species and the active metal, occur at temperatures higher than 150 degrees C. The kinetics of growth of the surface films on Li show an inverse logarithmic behavior, expected for thin surface films with which the rate-limiting step of their growth depends on ions transport across the film.

We report on a discovery of fast cathode materials, ternary Chevrel phases (CPs), CuyMo6S8, for rechargeable magnesium batteries; the related electrochemical process displays a unique coupling between reversible Mg insertion, and Cu extrusion/ reinsertion; this coupling results in an entirely new intercalation mechanism which combines the total chemical reversibility of the electrochemical reaction of MgxCuyMo6S8 with irreversibility of its separate stages once Cu extrusion stage is reached (in MgxCuyMo6S8: 0.5x + y > 4).

This work presents, for the first time, a general mechanism of a rhombohedral (R)-triclinic (T) phase transition in Chevrel Phases (CPs) with small cations (radius<1 A), which was unclear in spite of intensive studies of these important materials in the past. In contrast to previous interpretation of the R<-->T transition in some CPs as cation ordering, T-distortion is regarded here as a particular case of general adaptation of the framework to cation insertion, which includes the deformations of the coordination polyhedra and their tilting. The research is based on a combination of experimental studies (in-situ neutron diffraction at different temperatures) for one model compound, MgMo6Se8, and structural analysis for a variety of known CPs. This analysis shows that the structure flexibility is fundamentally different for the R and T forms. As a result of the lower flexibility, in the R form, a strict correlation exists between the compression of the framework along the -3 symmetry axis and the cation position in the structure (the so-called 'delocalization'). The decreasing delocalization in the R-CPs, which occurs on cooling, leads to excessive repulsion within the cations pairs (R-Cu1.8Mo6S8 case) or undesirable asymmetry in the cation polyhedra (R-MgMo6Se8 case). The higher flexibility of the T framework allows for relaxation of these structural strains by increasing the cation-cation distances and forming a more symmetric cation environment, sometimes with higher coordination number (CN), like CN=5 in the T-Fe2Mo6S8 type. Thus, this work also proposes possible driving forces for T-distortion in CPs.

Incorporation of electron accepting units (oxadiazole) into the 2,5-thienylene conjugated chain leads to a significant improvement in the n-doping-undoping redox stability of the resulting polymer.

The dependence of the electronic conductivity of activated carbon electrodes on their potential in electrolyte solutions was examined. Kapton polymer films underwent carbonization (1000 degrees C), followed by a mild oxidation process (CO(2) at 900 degrees C) for various periods of time, to obtain carbons of different pore structures. A specially designed cell was assembled in order to measure the conductivity of carbon electrodes at different potentials in solutions. When the carbon electrodes possessed molecular sieving properties, a remarkable dependence of their conductivity on their charging state was observed. Aqueous electrolyte solutions containing ions of different sizes were used in order to demonstrate this phenomenon. As the average pore size of the activated carbons was larger, their molecular sieving ability was lower, and the dependence of their conductivity on their charging state regained its classical form. This behavior is discussed herein.

We previously showed that, for neutral electrolytes of small cations and relatively larger anions, it is possible to design certain pore sizes in active carbons that are large enough to electroadsorb cations but too small to allow anion electroadsorption. This situation leads to an electrical double-layer (EDL) capacitance that is significant only at potentials that are negative to the potential of zero charge (PZC); hence, much smaller capacitance is measured at potentials positive to the PZC. It was found that when the electrolyte is a strong acid (e.g., H(2)SO(4), HCl), a considerable capacitance is observed at positive potentials, even when the average pore size is too small to allow the insertion of large anions in neutral electrolyte solutions. This effect disappears when the pore size becomes considerably larger than the size of the ions. In this case, the EDL capacitance at positive potentials for both neutral and acidic solutions is comparable. The following four-step mechanism was found to comply best with the experimental data: (1) By acid catalysis, the protons form carbonium species within the conjugated carbon network. (2) The anions react with the carbonium ions, providing uncharged species in an activated state, which are chemibound as surface groups to the walls of the pores. (3) Because these surface groups are effectively much smaller in size than are the charged ions, they can migrate by chemical bond exchange within the carbon skeleton via constrictions (known to exist in microporous and molecular sieving carbons), which are too narrow to accommodate hydrated charged species. (4) Upon reaching wider spaces, the uncharged species are reionized and solvated by water molecules, which can fill small pores. The justification for the above mechanism is thoroughly discussed and demonstrated by the experimental results.

This paper deals with a study of the shape of the chronoamperometric response (current, I, vs time, t) and, eventually, the mechanism of Li-ions insertion and deinsertion to/from composite graphite electrodes obtained by a small-amplitude (incremental) technique, such as potentiostatic intermittent titration (PITT). The dependences of log I, the Cottrell parameter It(1/2), and the differential parameter d log I/d log t on the process duration (vs log t) were carefully examined both for single- and two-phase coexistence domains. log I vs log t curves for single-phase domains were characterized by a single monotonic curve with a gradually increasing slope. In contrast, the same curves for two-phase domains consist of two sequential downward concave lines. Both types of response were explained by using the cell-impedance-control model. To separate the contributions of solid-state diffusion, Ohmic drops, and slow interfacial charge-transfer kinetics to the chronoamperometric response, the data were presented in the form of the inverse Cottrell parameter, (It(1/2))(-1) vs t(-1/2), from which the chemical diffusion coefficient (D) could be obtained. Refined values of D for Li insertion into graphite obtained herein agree very well with values of the component diffusion coefficient obtained from quasielastic neutron scattering for Li insertion into HOPG, reported in the literature.

Electrochemical insertion of Mg ions into Mo6S8 Chevrel phase is a unique, model system for studying the nature of the energetic inhomogeneity of the host sites suitable for ions accommodation. We show that the two energy state model can be successfully used for describing the very specific Mg ions insertion kinetics into the host, in particular, as relates to a drastic increase of Mg ions mobility in the vicinity of the critical potential of 1.25 V (vs Mg). This is accompanied by very pronounced changes of the impedance spectra. On the other hand, similar behavior of impedance spectra could be obtained for geometrically nonhomogeneous intercalation electrodes, comprising a distribution of thicknesses. One can frequently meet both these cases in practice for a vast variety of intercalation electrodes (e.g., for lithiated graphite, composite Li(x)MO2, M = Mn, Ni, Co, etc.). In this paper, we developed a methodology aimed at a reliable distinction between the two alternatives, based on complex impedance and complex capacitance analysis.

A sonochemical process has been developed for the insertion of tin nanoparticles into mesoporous carbon, giving a product which was used as a building block for the anode of a rechargeable Li battery; the electrode could deliver a reversible capacity of 400 mAh gr(-1)(C + Sn) at 100% cycling efficiency, which is higher than that of graphite electrodes.

A revolution in modern electronics has led to the miniaturization and evolution of many portable devices, such as cellular telephones and laptop computers, since the 1980s. This has led to an increasing demand for new and compatible energy storage technologies. Furthermore, a growing awareness of pollution issues has provided a strong impetus for the science and technology community to develop alternatives with ever-higher energy densities, with the ultimate goal of being able to propel electric vehicles. Magnesium's thermodynamic properties make this metal a natural candidate for utilization as an anode in high-energy-density, rechargeable battery systems. We report herein on the results of extensive studies on magnesium anodes and magnesium insertion electrodes in nonaqueous electrolyte solutions. Novel, rechargeable nonaqueous magnesium battery systems were developed based on the research. This work had two major challenges: one was to develop electrolyte solutions with especially high anodic stability in which magnesium anodes can function at a high level of cycling efficiency; the other was to develop a cathode that can reversibly intercalate Mg ions in these electrolyte systems. The new magnesium batteries consist of Mg metal anodes, an electrolyte with a general structure of Mg(AlX(3-n)R(n)R')(2) (R',R = alkyl groups, X = halide) in ethereal solutions (e.g., tetrahydrofuran, polyethers of the "glyme" family), and Chevrel phases of MgMo(3)S(4) stoichiometry as highly reversible cathodes. With their practical energy density expected to be >60 Wh/Kg, the battery systems can be cycled thousands of times with almost no capacity fading. The batteries are an environmentally friendly alternative to lead-acid and nickel-cadmium batteries and are composed of abundant, inexpensive, and nonpoisonous materials. The batteries are expected to provide superior results in large devices that require high-energy density, high cycle life, a high degree of safety, and low-cost components. Further developments in this field are in active progress., (Copyright 2003 The Japan Chemical Journal Forum and Wiley Periodicals, Inc., Chem Rec 3: 61-73; 2003: Published online in Wiley InterScience (www.interscience.wiley.com) DOI 10.1002/tcr.10051)

The thermodynamic properties of magnesium make it a natural choice for use as an anode material in rechargeable batteries, because it may provide a considerably higher energy density than the commonly used lead-acid and nickel-cadmium systems. Moreover, in contrast to lead and cadmium, magnesium is inexpensive, environmentally friendly and safe to handle. But the development of Mg batteries has been hindered by two problems. First, owing to the chemical activity of Mg, only solutions that neither donate nor accept protons are suitable as electrolytes; but most of these solutions allow the growth of passivating surface films, which inhibit any electrochemical reaction. Second, the choice of cathode materials has been limited by the difficulty of intercalating Mg ions in many hosts. Following previous studies of the electrochemistry of Mg electrodes in various non-aqueous solutions, and of a variety of intercalation electrodes, we have now developed rechargeable Mg battery systems that show promise for applications. The systems comprise electrolyte solutions based on Mg organohaloaluminate salts, and Mg(x)Mo3S4 cathodes, into which Mg ions can be intercalated reversibly, and with relatively fast kinetics. We expect that further improvements in the energy density will make these batteries a viable alternative to existing systems.

AS101, a synthetic organotellurium compound, was found to have immunomodulating properties by initiation of cytokine production in vitro and in vivo. Phase I/II clinical trials currently in progress on AIDS and cancer patients treated with AS101 show significant increases in various immunological parameters, with minimal toxicity. Recently, AS101 and the protein kinase C (PKC) inducer, phorbol myristate acetate (PMA), were shown to synergize in the secretion of interleukin-2 (IL-2) and colony-stimulating factor (CSF) in vitro, by human and mouse lymphoid cells. The bryostatins, a group of natural macrocyclic lactones isolated from marine invertebrates (Bugula neritina) have been reported to be potent PKC activators with no tumour promoting activity. In this study, we investigated the synergistic effect of AS101 and a partially purified preparation of bryostatin on the production of several cytokines. Our data confirm the presence of synergism, which greatly enhances cell proliferation, IL-2, tumour necrosis factor (TNF) and interferon-gamma (IFN-gamma) secretion by human mononuclear cells (MNC) and the production of IL-2 and TNF by mouse cells. The absence of tumour-promoting activity of the bryostatins makes them particularly good candidates, in combination with AS101, for immunomodulation in vivo in clinically immunosuppressed conditions.