Amorphous,nanocrystalline and crystalline calcium carbonates in biological materials

Raman spectroscopy is a powerful tool in identifying different calcium carbonate polymorphs. Here, the method is applied to cultured pearls from freshwater (genus Hyriopsis) and marine bivalve species (Pinctada maxima) as well as to shells of Diplodon chilensis patagonicus bivalves. Raman spectra for vaterite, detected for the first time in an adult shell, and amorphous calcium carbonate (ACC) are discussed. Results for ACC are compared with those of synthetically produced ACC and with the Raman spectroscopic features of stable biogenic ACC from the crustacean Porcellio scaber. Decomposition of the most intense signal of all calcium carbonate polymorphs—the ν₁ symmetric stretching mode of the carbonate ion—leads to the identification of two polymorphs within the ACC areas: a mixure of an amorphous and a crystalline fraction. The amorphous phase is characterised by a broad peak in the region of the lattice modes, which is composed of two distinct lattice modes with very high full‐widths at half‐maximum (FWHMs). The FWHMs of most of the crystalline fractions (in the range of 6.3–10.7 cm⁻¹) are too high for well‐crystallised materials and support reports of nanocrystalline calcium carbonate polymorph clusters in ACC. Crystallinity indices of different samples are calculated and found to be useful to describe roughly the state of crystallisation in the ACC areas. Copyright © 2010 John Wiley & Sons, Ltd.     

Effect of electrolyte temperature on the formation of self-organized anodic niobium oxide microcones in hot phosphate-glycerol electrolyte

Nanoporous niobium oxide films with microcone-type surface morphology were formed by anodizing at 10 V in glycerol electrolyte containing 0.6 mol dm⁻³ K₂HPO₄ and 0.2 mol dm⁻³ K₃PO₄ in a temperature range of 428-453 K. The microcones appeared after prolonged anodizing, but the required time was largely reduced by increasing electrolyte temperature. The anodic oxide was initially amorphous at all temperatures, but crystalline oxide nucleated during anodizing. The anodic oxide microcones, which were crystalline, appeared on surface as a consequence of preferential chemical dissolution of initially formed amorphous oxide. The chemical dissolution of an initially formed amorphous layer was accelerated by increasing the electrolyte temperature, with negligible influence of the temperature on the morphology of microcones up to 448 K.     

In situ formation of low friction ceramic coatings on carbon steel by plasma electrolytic oxidation in two types of electrolytes

In situ formation of ceramic coatings on Q235 carbon steel was achieved by plasma electrolytic oxidation (PEO) in carbonate electrolyte and silicate electrolyte, respectively. The surface and cross-section morphology, phase and elemental composition of PEO coatings were examined by means of scanning electron microscopy (SEM), X-ray diffraction (XRD) and energy-dispersive X-ray spectroscopy (EDS). The bond strength of the coating was determined using a direct pull-off test. The hardness as well as tribological properties of the ceramic coating was primarily studied. The results indicated that the coating obtained in carbonate electrolyte was Fe₃O₄, while the coating achieved from silicate electrolyte was proved to be amorphous. Both kinds of coatings showed coarse and porous surface. The Fe₃O₄ coatings obtained in carbonate electrolyte showed a high bonding strength to the substrate up to 20 ± 2 MPa and the value was 15 ± 2 MPa for the amorphous coatings obtained in carbonate electrolyte. The micro hardness of the amorphous coating and the Fe₃O₄ coating was 1001 Hv and 1413 Hv, respectively, which was more than two and three times as that of the Q235 alloy substrate (415 Hv). The friction coefficient exhibited by amorphous coating and Fe₃O₄ coating was 0.13 and 0.11, respectively, both lower than the uncoated Q235 substrate which ranged from 0.17 to 0.35.     

Metallo-organic decomposition derived (Ca, Sr)ZrO3 dielectric thin films on Pt coated Si substrate

Metallo-organic decomposition derived dielectric thin films of calcium zirconate doped with various concentrations of strontium ((Ca, Sr)ZrO₃) were prepared on Pt coated silicon substrate. Mainly in this paper, we present the investigations of their structural developments and present their electric and dielectric properties as well. The structural developments show that the CaZrO₃ film has amorphous structure with carbonate existing when annealed at 600 °C, while annealed at 650 °C and above, the carbonate is decomposed and those films crystallize into perovskite phase without preferred orientation. In addition, the prepared (Ca, Sr)ZrO₃ films with their Zr-O bonds affected by strontium doping are homogenous and stable as solid solutions in any concentration of strontium and all Bragg diffraction characteristics for the films shift downward with the increase in the concentration of strontium. Moreover, the electric properties show that the (Ca, Sr)ZrO₃ films have very low leakage current density and high breakdown strength; typically, the CaZrO₃ film annealed at 650 °C has the leakage current density approximately 9.5 × 10⁻⁸ A cm⁻² in the field strength of 2.6 MV cm⁻¹. Furthermore, the dielectric properties show that their dielectric constants are higher than 12.8 with very little dispersion in the frequency range from 100 Hz to 1 MHz and are independent of applied dc bias as well. The dielectric properties, in combination with the electric properties, make the materials promising candidates for high-voltage and high-reliability capacitor applications.     

Correlation between impurities in Fe-Si amorphous layers synthesized by Fe implantation and photoluminescence property of β-FeSi2 precipitates in Si

Completely amorphous Fe-Si layers are formed by Fe implantation into Si substrate at a dosage of 5×10¹⁵ cm⁻² using a metal vapor vacuum arc (MEVVA) ion source under 80 kV extraction voltage and cryogenic temperature. After thermal annealing, β-FeSi₂ precipitates are formed in Si matrix. The influence of impurities in these amorphous Fe-Si layers on the photoluminescence (PL) from β-FeSi₂ precipitates is investigated. PL is found to be significantly enhanced by optimizing the impurity concentration and annealing scheme. After 60 s of rapid thermal annealing (RTA) at 900 °C, β-FeSi₂ precipitates in medium boron-doped Si substrate give the strongest PL intensity without boron out-diffusion from them.     

Effects of Al2O3 nanofiller and EC plasticizer on the ionic conductivity enhancement of solid PEO-LiCF3SO3 solid polymer electrolyte

A solid polymer electrolyte (SPE) is synthesized by solution casting technique. The SPE uses poly(ethylene oxide) PEO as a host matrix doped with lithium triflate (LiCF₃SO₃), ethylene carbonate (EC) as plasticizer and nano alumina (Al₂O₃) as filler. The polymer electrolytes are characterized by Impedance Spectroscopy (IS) to determine the composition of the additive which gives the highest conductivity for each system. At room temperature, the highest conductivity is obtained for the composition PEO-LiCF₃SO₃-EC-15%Al₂O₃ with a value of 5.07 10^− 4 S/cm. The ionic conductivity of the polymer electrolytes increases with temperature and obeys the Arrhenius law. X-ray diffraction (XRD) and differential scanning calorimetry (DSC) studies indicate that the conductivity increase is due to an increase in amorphous content which enhances the segmental flexibility of polymeric chains and the disordered structure of the electrolyte. Fourier transform infrared spectroscopy (FTIR) spectra show the occurrence of complexation and interaction among the components. Scanning electron microscopy (SEM) images show the changes morphology of solid polymer electrolyte.     

Physico-chemical, optical and electrochemical properties of iron oxide thin films prepared by spray pyrolysis

Iron oxide thin films were prepared by spray pyrolysis technique onto glass substrates from iron chloride solution. They were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and (UV-vis) spectroscopy. The films deposited at T_s ≤ 450 °C were amorphous; while those produced at T_sub = 500 °C were polycrystalline α-Fe₂O₃ with a preferential orientation along the (1 0 4) direction. By observing scanning electron microscopy (SEM), it was seen that iron oxide films were relatively homogeneous uniform and had a good adherence to the glass substrates. The grain size was found (by RX) between 19 and 25 nm. The composition of these films was examined by X-ray photoelectron spectroscopy and electron probe microanalysis (EPMA). These films exhibited also a transmittance value about 80% in the visible and infrared range. The cyclic voltammetry study showed that the films of Fe₂O₃ deposited on ITO pre-coated glass substrates were capable of charge insertion/extraction when immersed in an electrolyte of propylene carbonate (PC) with 0.5 M LiCLO₄.     

碳酸钙在溶液中的演化机理

以EDTA作为添加剂,在CaCl₂/NaCO₃混合液中采用共沉淀法制备了碳酸钙,并探讨它在母液中的演化机理. 热力学和动力学计 算表明虽然形成无定形碳酸钙(ACC)的驱动力小于方解石和球霰石,但在共沉淀反应的初始阶段ACC的形核速率高于方解石和球霰石. 随着陈化时间的延长,最新生成的碳酸钙成为球霰石和方解石异相形核的活性点. 通过SEM发现ACC和球霰石在母液中通过溶解-再结晶机理转化成方解石. 此外,EDTA添加剂不仅提高了ACC和球霰石的稳定性,而且有助于碳酸钙在母液中陈化7天后转化成长棒状、菱形的方解石晶体. 如果将碳酸钙放置在空气介质中,ACC和球霰石也可以通过溶解-再结晶反应转化成方解石,但其转化速率低于溶液介质.     

Effect of hot pressing on the ionic conductivity of the PEO/LiCF3SO3 based electrolyte membranes

PEO/LiCF₃SO₃ (LiTFS) /Ethylene carbonate (EC) polymer electrolyte membranes were prepared with a solution casting method followed by a hot pressing process. The effect of the hot pressing process on the in-plane conductivity of the PEO electrolyte membranes was evaluated using a four-electrode AC impedance method. The composition, morphology, and microstructure of the composite polymer electrolyte were characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The AC impedance measurement results indicate that the hot pressing process can increase the room temperature conductivity of the membranes 14 times to 1.7 × 10^− 3 S cm^− 1 depending upon the duration of the hot pressing process. The SEM, FTIR, XRD, and DSC results indicate that the hot pressing process could increase the amorphous part of the polymer electrolyte membrane or convert large spherulite crystals into nano-sized crystals.     

New Fe-based amorphous compound powder cores with superior DC-bias properties and low loss characteristics

The Fe–Si–B–P–C metallic glassy alloys exhibit relatively high glass forming ability (GFA) as well as good soft magnetic properties such as ultra-low core loss. In this paper, the metallic glassy alloy (Fe_0.76Si_0.09B_0.10P_0.05)₉₈C₂ has been newly developed. A new Fe-based amorphous compound powder was prepared from FeSiB amorphous powder by crushing the amorphous ribbons as the first magnetic component and FeSiBPC metallic glassy powder by water atomization as the second magnetic component. Subsequently by adding organic and inorganic binders to the compound powder and cold pressing, the new Fe-based amorphous compound powder cores were fabricated. These new Fe-based amorphous compound powder cores combine the superior DC-bias properties and the excellently low core loss. The core loss of 453 kW/m³ at B_m=0.1 T and f=100 kHz was obtained when the mass ratio of FeSiB/FeSiBPC equals 3:2, and meanwhile the DC-bias properties of the new Fe-based amorphous compound powder cores just increased by 10% at H=100 Oe for μ=60 compared to those of the FeSiBPC powder cores. In addition, with the increase in the content of the FeSiPC metallic glassy powder, the core loss tends to decrease.     

Study of HfSiO film prepared by electron beam evaporation for high-k gate dielectric applications

The purpose of this paper is to report some experimental results with HfSiO films formed on silicon substrates by electron beam evaporation (EB-PVD) and annealed at different temperatures. The images of atomic force microscope (AFM) indicated that HfSiO film annealed at 900 °C was still amorphous, with a surface roughness of 0.173 nm. X-ray photoelectron spectroscopy (XPS) analysis revealed that the chemical composition of the film was (HfO₂)₃(SiO₂) and Hf-Si-O bonds existed in the annealed film. Electrical measurements showed that the equivalent oxide thickness (EOT) was 4 nm, the dielectric constant was around 6, the breakdown voltage was 10 MV/cm, the fixed charge density was −1.2 × 10¹² cm⁻², and the leakage current was 0.4 μA/cm² at the gate bias of 2 V for 6 nm HfSiO film. The annealing after deposition effectively reduced trapping density and the leakage current, and eliminated hysteresis in the C-V curves. Annealing also induced SiO₂ growth at the interface.     

Transparent and conducting Zn-Sn-O thin films prepared by combinatorial approach

Zn-Sn-O (ZTO) films with continuous compositional gradient of Sn 16-89 at.% were prepared by co-sputtering of two targets of ZnO and SnO₂ in a combinatorial method. The resistivities of the ZTO films were severely dependent on oxygen content in sputtering gas and Zn/Sn ratio. Except for the films with Sn 16 at.%, all the as-prepared films were amorphous and maintaining the stable amorphous states up to the annealing temperature of 450 °C. Annealing at 650 °C resulted in crystallization for all the composition, in which ZnO, Zn₂SnO₄, ZnSnO₃, and SnO₂ peaks were appeared successively with increasing Sn content. Above Sn 54 at.%, the ZTO films were deduced to have a local structure mixed with ZnSnO₃ and SnO₂ phases which were more conductive and stable in thermal oxidation than ZnO and Zn₂SnO₄ phases. The lowest resistivity of 1.9 × 10⁻³ Ω cm was obtained for the films with Sn 89 at.% when annealed at 450 °C in a vacuum. The carrier concentrations of the amorphous ZTO films that contained Sn contents higher than 36 at.% and annealed at 450 °C in a vacuum were proportional to the Sn contents, while the Hall mobilities were insensitive to Sn contents and leveling in the range of 23-26 cm²/V s.     

A study of water releases in ground (GCC) and precipitated (PCC) calcium carbonates

Precipitate calcium carbonates (PCCs) are important industrial products mainly used as fillers. Because of their regular, synthesized characteristics (e.g. grain shape or grain size distribution) PCCs are distinct from natural ground calcium carbonates (GCCs). A thermal study on GCC samples showed only the presence of surface physisorbed water with a monotonic weight loss up to the carbonate decomposition. In the case of PCC samples, two supplementary water releases were observed. The first one appeared at around 525 K and the second one at around 725 K. The nature of the water present in two different PCC samples was investigated by thermal analyses (thermogravimetric and Karl Fischer analyses), Rietveld analyses on X-rays powder diffraction, infrared and Raman spectroscopies and solid state ¹H MAS NMR. The second water release at about 725 K was clearly identified as being portlandite dehydration. Ca(OH)₂ was present in the PCC in an amorphous state. Its crystallization occurred simultaneously to the first water release at about 525 K. Structural effects observed on calcite during the first water release led to the assignment to structural water molecules inserted in the structure of calcite.     

Preparation of nanocrystalline MnFe2O4 by doping with Ti ions using solid-state reaction route

Nanostructured manganese ferrites (MnFe₂O₄) with diameters in the range of 45–30 nm were synthesized by Ti⁴⁺ ion doping, using conventional solid-state reaction route. The substitution of Ti⁴⁺ ions created vacancies at Mn²⁺ sites and the coupling of ferrimagnetically active oxygen polyhedra was broken. This created nanoscale regions of ferrites. A reduction of magnetization for decreasing particle size was observed. Coercivity showed an increasing trend. This was explained as arising due to multidomain/monodomain magnetic behaviour of magnetic nanoparticles. DC resistivities of the doped specimens indicated the presence of an interfacial amorphous phase formed by the nanoparticles. Zero-field cooled and field-cooled curves from 30 nm sized particles showed a peak at T_B (∼125 K), typical of superparamagnetic blocking temperature.     

Electrical and optical properties of Ga doped zinc oxide thin films deposited at room temperature by continuous composition spread

Ga doped ZnO (GZO) thin films were deposited on glass substrates at room temperature by continuous composition spread (CCS) method. CCS is thin films growth method of various Ga_xZn_1−xO(GZO) thin film compositions on a substrate, and evaluating critical properties as a function position, which is directly related to material composition. Various compositions of Ga doped ZnO deposited at room temperature were explored to find excellent electrical and optical properties. Optimized GZO thin films with a low resistivity of 1.46 × 10⁻³ Ω cm and an average transmittance above 90% in the 550 nm wavelength region were able to be formed at an Ar pressure of 2.66 Pa and a room temperature. Also, optimized composition of the GZO thin film which had the lowest resistivity and high transmittance was found at 0.8 wt.% Ga₂O₃ doped in ZnO.     

Mechanism of aluminum hydroxide layer formation by surface modification of aluminum

In this study, a new, relatively simple and rapid fabrication method for forming an Al(OH)₃ film on Al substrates was demonstrated. This method, i.e., alkali surface modification, is simply comprised of dipping the substrate in a 5 × 10⁻³ M NaOH solution at 80 °C for 1 min and then immersing it in boiling water for 30 min. After alkali surface modification, an Al(OH)₃ film was formed on Al substrate, and its chemical state and crystal structure were confirmed by XPS and TEM. The Al(OH)₃ layer was composed of three regions: an amorphous-rich region, a region of mixed amorphous and crystal domains, and a crystalline-rich region near the Al(OH)₃ layer surface.     

Preparation and properties of a gel polymer electrolyte system based on poly-ε-caprolactone containing 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Gel polymer electrolytes (GPE) obtained by immobilizing a solution of zinc triflate (ZnTr) in an ionic liquid, namely 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide [emim][Tf₂N] within a biodegradable polymeric matrix of poly-ε-caprolactone (PCL) were prepared by a simple solvent cast technique for different concentrations of the ionic liquid. The electrolyte with the composition 75 wt% PCL: 25 wt% ZnTr+100 wt% [emim][Tf₂N] showed the highest ionic conductivity of 1.1×10⁻⁴ S cm⁻¹ at 25 °C and favored by the rich amorphous phase of the GPE as confirmed from room temperature X-ray diffraction analysis (XRD). The morphology of the GPE was examined using scanning electron microscopy (SEM) which revealed the homogeneity of the prepared GPE system. The temperature dependence of electrical conductivity of the GPE followed the Arrhenius behavior. The Zn²⁺ ionic transport number has been determined to be ~0.62 which denotes the predominant contribution of zinc ion towards total ionic conductivity. The electrochemical stability window of GPE is found to be 2.5 V with a thermal stability upto 200 °C. This eco-friendly and safe electrolyte may be used to fabricate compostable batteries, in future, with a suitable selection of other components of the battery system.     

Improvement of the magnetic properties of barium hexaferrite nanopowders using modified co-precipitation method

Barium hexaferrite BaFe₁₂O₁₉ powders have been synthesized using the modified co-precipitation method. Modification was performed via the ultrasonication of the precipitated precursors at room temperature for 1 h and the additions of the 2% KNO₃, surface active agents and oxalic acid. The results revealed that single phase magnetic barium hexaferrite was formed at a low annealing temperature of 800 °C for 2 h with the Fe³⁺/Ba²⁺ molar ratio 8. The microstructure of the powders appeared as a homogeneous hexagonal platelet-like structure using 2% KNO₃ as the crystal modifier. A saturation magnetization (60.4 emu/g) was achieved for the BaFe₁₂O₁₉ phase formed at 1000 °C for 2 h with Fe³⁺/Ba²⁺ molar ratio 8 using 5 M NaOH solution at pH 10 in the presence of 2% KNO₃. Moreover, the saturation magnetization was 52.2 emu/g for the precipitated precursor at Fe³⁺/Ba²⁺ molar ratio 12 in was achieved for the precipitated precursor ultrasonicated for 1 h and then annealed at 1200 °C for 2 h. Coercivities from 956.9 to 4558 Oe were obtained at different synthesis conditions.     

Upconversion luminescence of colloidal solution of Y2O3 nano-particles doped with trivalent rare-earth ions

We have studied upconversion luminescence of colloidal solution of Y₂O₃ nano-particles codoped with 1 mol% Er³⁺ and 5 mol% Yb³⁺. Y₂O₃ nano-particles codoped with 1 mol% Er³⁺ and 5 mol% Yb³⁺ show sintering and agglomeration, because they are synthesized by firing a hydroxy carbonate precursor. Colloidal solution of Y₂O₃ nano-particles codoped with 1 mol% Er³⁺ and 5 mol% Yb³⁺ is prepared through two-step dispersion process and the average diameter of the primary nano-particles is about 50 nm. Under excitation with 980-nm laser diode, upconversion luminescence of colloidal solution of the primary Y₂O₃ nano-particles codoped with 1 mol% Er³⁺ and 5 mol% Yb³⁺ in methyl isobuthyl ketone strongly appeared near 660 nm and weakly near 550 nm.     

Luminescence characterization and electron beam induced chemical changes on the surface of ZnAl2O4:Mn nanocrystalline phosphor

Luminescence characteristics and surface chemical changes of nanocrystalline Mn²⁺ doped ZnAl₂O₄ powder phosphors are presented. Stable green cathodoluminescence (CL) or photoluminescence (PL) with a maximum at ∼512 nm was observed when the powders were irradiated with a beam of high energy electrons or a monochromatic xenon lamp at room temperature. This green emission can be attributed to the ⁴T₁ → ⁶A₁ transitions of the Mn²⁺ ion. Deconvoluted CL spectra resulted in two additional emission peaks at 539 and 573 nm that may be attributed to vibronic sideband and Mn⁴⁺ emission, respectively. The luminescence decay of the Mn²⁺ 512 nm emission under 457 nm excitation is single exponential with a lifetime of 5.20 ± 0.11 ms. Chemical changes on the surface of the ZnAl₂O₄:Mn²⁺ phosphor during prolonged electron beam exposure were monitored using Auger electron spectroscopy. The X-ray photoelectron spectroscopy (XPS) was used to determine the chemical composition of the possible compounds formed on the surface as a result of the prolonged electron beam exposure. The XPS data suggest that the thermodynamically stable Al₂O₃ layer was formed on the surface and is possibly contributing to the CL stability of ZnAl₂O₄:Mn phosphor.