A Comparative XPS, UV PES, NEXAFS, and DFT Study of the Electronic Structure of the Salen Ligand in the H2(Salen) Molecule and the [Ni(Salen)] Complex.

A comparative study of the electronic structure of the salen ligand in the H2(Salen) molecule and the [Ni(Salen)] complex was performed using the experimental methods of XPS, UV PES, and NEXAFS spectroscopy along with DFT calculations. Significant chemical shifts of +1.0 eV (carbon), +1.9 eV (nitrogen), and -0.4 eV (oxygen) were observed in the 1s PE spectra of the salen ligand atoms when passing from a molecule to a complex, unambiguously indicating a substantial redistribution of the valence electron density between these atoms. It is proposed that the electron density transfer to the O atoms in [Ni(Salen)] occurred not only from the Ni atom, but also from the N and C atoms. This process seemed to be realized through the delocalized conjugated π-system of the phenol C 2p electronic states of the ligand molecule. The DFT calculations (total and partial DOS) for the valence band H2(Salen) and [Ni(Salen)] described well the spectral shape of the UV PE spectra of both compounds and confirmed their experimental identification. An analysis of the N and O 1s NEXAFS spectra clearly indicated that the atomic structure of the ethylenediamine and phenol fragments was retained upon passing from the free salen ligand to the nickel complex.

Features of Phase Formation of Pyrochlore-type Ceramics Bi2Mg(Zn)1-x Ni x Ta2O9.

The phase formation of complex pyrochlores (space group Fd-3m) Bi2Mg(Zn)1-x Ni x Ta2O9 was investigated during solid-phase synthesis. It was found that the pyrochlore phase precursor in all cases was α-BiTaO4. The pyrochlore phase synthesis reaction proceeds mainly at temperatures above 850-900 °C and consists in the interaction of bismuth orthotantalate with a transition element oxide. The influence of magnesium and zinc on the course of pyrochlore synthesis was revealed. The reaction temperatures of magnesium and nickel (800 and 750 °C, respectively) were determined. The change in the pyrochlore unit cell parameter depending on the synthesis temperature was analyzed for both systems. Nickel-magnesium pyrochlores are characterized by a porous dendrite-like microstructure with a grain size of 0.5-1.0 microns, and the porosity of the samples reaches 20 percent. The calcination temperature does not significantly affect the microstructure of the samples. Prolonged calcination of the preparations leads to the coalescence of grains with the formation of larger particles. Nickel oxide has a sintering effect on ceramics. The studied nickel-zinc pyrochlores are characterized by a low-porous dense microstructure. The porosity of the samples does not exceed 10%. The optimal conditions for obtaining phase-pure pyrochlores (1050 °C and 15 h) were determined.

Effect of Fe-Doping on Thermal Expansion and Stability of Bismuth Magnesium Tantalate Pyrochlorere.

A continuous series of solid solutions (Bi1.5Mg0.75-xFexTa1.5O7±Δ (x = 0-0.75)) with the pyrochlore structure were synthesized with the solid-phase method. It was shown that iron, like magnesium, is concentrated in the structure in the octahedral position of tantalum. Doping with iron atoms led to an increase in the upper limit of the thermal stability interval of magnesium-containing pyrochlore from 1050 °C (x = 0) up to a temperature of 1140 °C (x = 1). The unit cell constant a and thermal expansion coefficient (TEC) increase uniformly slightly from 10.5018 Å up to 10.5761 Å and from 3.6 up to 9.3 × 10-6 °C-1 in the temperature range 30-1100 °C. The effect of iron(III) ions on the thermal stability and thermal expansion of solid solutions was revealed. It has been established that the thermal stability of iron-containing solid solutions correlates with the unit cell parameter, and the lower the parameter, the more stable the compound. The TEC value, on the contrary, is inversely proportional to the cell constant.

Cu, Mg Codoped Bismuth Tantalate Pyrochlores: Crystal Structure, XPS Spectra, Thermal Expansion, and Electrical Properties.

The pyrochlore-type solid-solution formation in a Bi1.6Mg0.8-xCuxTa1.6O7.2-Δ system, synthesized for the first time, is observed at x ≤ 0.56. High-temperature X-ray diffraction showed that the pyrochlore phase exists in air up to 1080 °C, where its thermal decomposition leads to the segregation of (Mg,Cu)Ta2O6. The thermal expansion coefficients of the end member, Bi1.6Mg0.24Cu0.56Ta1.6O7.2-Δ, increase from 3.3 × 10-6 °C-1 at room temperature up to 8.7 × 10-6 °C-1 at 930 °C. Rietveld refinement confirmed that the pyrochlore crystal structure is disordered with space group Fd3̅m:2 (Z = 8, no. 227). Doping with copper results in a modest expansion of the cubic unit cell, promotes sintering of the ceramic materials, and induces their red-brown color. X-ray photoelectron spectroscopy demonstrated that the states of Bi(III) and Mg(II) are not affected by doping, and the effective charge of tantalum cations is lower than +5, while the Cu(II) states coexist with Cu(I). The electron spin resonance spectra display a single line with g = 2.2, ascribed to the dipole-broadened Cu2+ signal. The dielectric permittivity of Bi1.6Mg0.8-xCuxTa1.6O7.2-Δ ceramics may achieve up to ∼105, with the dielectric loss tangent varying in the range from 0.2 up to 12. Multiple dielectric relaxations are found at room temperature and above for all samples.

The Identification of Cu-O-C Bond in Cu/MWCNTs Hybrid Nanocomposite by XPS and NEXAFS Spectroscopy.

The results of the research of a composite based on multi-walled carbon nanotubes (MWCNTs) decorated with CuO/Cu2O/Cu nanoparticles deposited by the cupric formate pyrolysis are discussed. The study used a complementary set of methods, including scanning and transmission electron microscopy, X-ray diffractometry, Raman, and ultrasoft X-ray spectroscopy. The investigation results show the good adhesion between the copper nanoparticles coating and the MWCNT surface through the oxygen atom bridge formation between the carbon atoms of the MWCNT outer graphene layer and the oxygen atoms of CuO and Cu2O oxides. The formation of the Cu-O-C bond between the coating layer and the outer nanotube surface is clearly confirmed by the results of the O 1s near edge X-ray absorption fine structure (NEXAFS) and X-ray photoelectron spectroscopy (XPS) of the Cu/MWCNTs nanocomposite. The XPS measurements were performed using a laboratory spectrometer with sample charge compensation, and the NEXAFS studies were carried out using the synchrotron radiation of the Russian-German dipole beamline at BESSY-II (Berlin, Germany) and the NanoPES station at the Kurchatov Center for Synchrotron Radiation and Nanotechnology (Moscow, Russia).

Calcite Nanotuned Chitinous Skeletons of Giant Ianthella basta Marine Demosponge.

Marine sponges were among the first multicellular organisms on our planet and have survived to this day thanks to their unique mechanisms of chemical defense and the specific design of their skeletons, which have been optimized over millions of years of evolution to effectively inhabit the aquatic environment. In this work, we carried out studies to elucidate the nature and nanostructural organization of three-dimensional skeletal microfibers of the giant marine demosponge Ianthella basta, the body of which is a micro-reticular, durable structure that determines the ideal filtration function of this organism. For the first time, using the battery of analytical tools including three-dimensional micro-X-ray Fluorescence (3D-µXRF), X-ray diffraction (XRD), infra-red (FTIR), Raman and Near Edge X-ray Fine Structure (NEXAFS) spectroscopy, we have shown that biomineral calcite is responsible for nano-tuning the skeletal fibers of this sponge species. This is the first report on the presence of a calcitic mineral phase in representatives of verongiid sponges which belong to the class Demospongiae. Our experimental data suggest a possible role for structural amino polysaccharide chitin as a template for calcification. Our study suggests further experiments to elucidate both the origin of calcium carbonate inside the skeleton of this sponge and the mechanisms of biomineralization in the surface layers of chitin microfibers saturated with bromotyrosines, which have effective antimicrobial properties and are responsible for the chemical defense of this organism. The discovery of the calcified phase in the chitinous template of I. basta skeleton is expected to broaden the knowledge in biomineralization science where the calcium carbonate is regarded as a valuable material for applications in biomedicine, environmental science, and even in civil engineering.

Novel Ni-Doped Bismuth-Magnesium Tantalate Pyrochlores: Structural and Electrical Properties, Thermal Expansion, X-ray Photoelectron Spectroscopy, and Near-Edge X-ray Absorption Fine Structure Spectra.

The samples of Ni-doped bismuth magnesium tantalate pyrochlores with the general formula Bi1.4(Mg1-x Ni x )0.7Ta1.4O6.3 (x = 0.3, 0.5, 0.7) were obtained by solid-phase synthesis. The crystal structure of the pyrochlore type (sp. gr. Fd3̅m:2) was clarified by the Rietveld method on the basis of X-ray powder diffraction data. The unit cell parameters increase with the decreasing nickel content in the range from 10.5319(1) to 10.5391(1) Å. The electronic state of atoms is established by the XPS method. According to XPS analysis, bismuth atoms have an effective charge of +3, nickel atoms +(2 + δ), and tantalum ions +(5 - δ). The coefficient of thermal expansion of the lattice of the samples was calculated from high-temperature X-ray structural measurements in the range of -180 to 1050 °C. The average values of linear TECs α in the temperature ranges of 30-570 and 600-1050 °C are 5.1 × 10-6 and 8.1 × 10-6 °C-1, respectively. The monotonicity of the change in the thermal expansion coefficient in the temperature range from -100 to 1050 °C indicates the absence of phase transformations. All samples are dielectric and exhibit high activation energies ∼2.0 eV, moderately high dielectric constants ∼24-28, and tangent dielectric losses ∼0.002 at 1 MHz and 21 °C. The electrical properties of the samples are described by a simple parallel equivalent scheme. The chemical composition of the materials has little effect on the polarizability of the medium or on the value of the activation energy of the conductivity. Ionic processes in investigated materials at frequencies 200-106 Hz and at temperatures 100-450 °C were not detected.

Thermal Expansion, XPS Spectra, and Structural and Electrical Properties of a New Bi2NiTa2O9 Pyrochlore.

A phase-pure nickel bismuth tantalate with pyrochlore structure was synthesized by a solid-phase synthesis method for the first time. The crystal structure of pyrochlore (refined formula Bi1.58Ni0.60Ta1.40O7, sp. gr. Fd-3m, a = 10.5343 Å, Z = 8) was clarified by the Rietveld method on the basis of X-ray powder diffraction (XRD) data. The crystallite size determined by the Scherrer method is ∼46 nm. The sample has an atypical pink-purple color. The electronic state of the atoms was investigated by XPS. According to XPS analysis, bismuth atoms have an effective charge of +3; nickel atoms, +(2 + δ); tantalum ions, +(5 - δ). The thermal expansion coefficient of the cell is calculated from high-temperature X-ray measurements in the range of 30-1200 °C. The thermal expansion coefficient (TEC) increases monotonically from 3.79 × 10-6 °C-1 (30 °C) to 8.32 × 10-6 °C-1 (990 °C). Above 1080 °C, the TEC decreases due to the thermal dissociation of pyrochlore with new NiTa2O6 phase formation. Ni-doped bismuth tantalate refers to dielectrics and exhibits a moderately high dielectric constant, ∼32, and low dielectric losses, ∼2 × 10-3 at 1 MHz and ∼30 °C. Above 300 °C, the dielectric losses and dielectric permittivity increase in the low-frequency region due to the activation of oxygen anions. It is found that the electrical characteristics of the sample are significantly affected by the ambient air humidity. An equivalent scheme which satisfactorily describes the electrical properties of the sample has been proposed.

The Structure and Chemical Composition of the Cr and Fe Pyrolytic Coatings on the MWCNTs' Surface According to NEXAFS and XPS Spectroscopy.

The paper is devoted to the structure and properties of the composite material based on multi-walled carbon nanotubes (MWCNTs) covered with pyrolytic iron and chromium. Fe/MWCNTs and Cr/MWCNTs nanocomposites have been prepared by the metal organic chemical vapor deposition (MOCVD) growth technique using iron pentacarbonyl and bis(arene)chromium compounds, respectively. Composites structures and morphologies preliminary study were performed using X-ray diffraction, scanning and transmission electron microscopy and Raman scattering. The atomic and chemical composition of the MWCNTs' surface, Fe-coating and Cr-coating and interface-(MWCNTs surface)/(metal coating) were studied by total electron yield method in the region of near-edge X-ray absorption fine structure (NEXAFS) C1s, Fe2p and Cr2p absorption edges using synchrotron radiation of the Russian-German dipole beamline (RGBL) at BESSY-II and the X-ray photoelectron spectroscopy (XPS) method using the ESCALAB 250 Xi spectrometer and charge compensation system. The absorption cross sections in the NEXAFS C1s edge of the nanocomposites and MWCNTs were measured using the developed approach of suppressing and estimating the contributions of the non-monochromatic background and multiple reflection orders radiation from the diffraction grating. The efficiency of the method was demonstrated by the example of the Cr/MWCNT nanocomposite, since its Cr2p NEXAFS spectra contain additional C1s NEXAFS in the second diffraction order. The study has shown that the MWCNTs' top layers in composite have no significant destruction; the MWCNTs' metal coatings are continuous and consist of Fe3O4 and Cr2O3. It is shown that the interface between the MWCNTs and pyrolytic Fe and Cr coatings has a multilayer structure: a layer in which carbon atoms along with epoxy -C-O-C- bonds form bonds with oxygen and metal atoms from the coating layer is formed on the outer surface of the MWCNT, a monolayer of metal carbide above it and an oxide layer on top. The iron oxide and chromium oxide adhesion is provided by single, double and epoxy chemical binding formation between carbon atoms of the MWCNT top layer and the oxygen atoms of the coating, as well as the formation of bonds with metal atoms.

Extreme biomimetics: Preservation of molecular detail in centimeter-scale samples of biological meshes laid down by sponges.

Fabrication of biomimetic materials and scaffolds is usually a micro- or even nanoscale process; however, most testing and all manufacturing require larger-scale synthesis of nanoscale features. Here, we propose the utilization of naturally prefabricated three-dimensional (3D) spongin scaffolds that preserve molecular detail across centimeter-scale samples. The fine-scale structure of this collagenous resource is stable at temperatures of up to 1200°C and can produce up to 4 × 10-cm-large 3D microfibrous and nanoporous turbostratic graphite. Our findings highlight the fact that this turbostratic graphite is exceptional at preserving the nanostructural features typical for triple-helix collagen. The resulting carbon sponge resembles the shape and unique microarchitecture of the original spongin scaffold. Copper electroplating of the obtained composite leads to a hybrid material with excellent catalytic performance with respect to the reduction of p-nitrophenol in both freshwater and marine environments.