LiNi0.5Mn1.5O4 cathode material by low-temperature solid-state method with excellent cycleability in lithium ion battery

LiNi_0.5Mn_1.5O₄ cathode material was synthesized from a mixture of LiCl, NiCl₂?6H₂O and MnCl₂?4H₂O with 70 wt.% oxalic acid by a low-temperature solid-state method. The calcination temperature was adjusted to form disorder Fd3m structure at 700-800 °C for 10 h.XRD patterns and FTIR spectroscopy showed that the LiNi_0.5Mn_1.5O₄ cathode material exhibited an impurity-free spinel Fd3m structure. Electrochemical property results revealed that the LiNi_0.5Mn_1.5O₄ cathode material charged at 1C rate to 4.9 V and discharged at 2 and 3 C to 3.5 V delivered initial capacity of 120 mAh/g and maintained a capacity retention over 80% at room temperature after 1000 charge/discharge cycles.     

The synthesis of LiBH4 films under low hydrogen pressure at ambient temperature

Lithium borohydride (LiBH₄) films were first fabricated under low hydrogen pressure (5-70 Pa) at ambient temperature by pulsed laser deposition (PLD). The atomistic structures and chemical compositions of the films were investigated. It was found that during the formation process of LiBH₄, the intermediate compound Li₂B₁₂H₁₂ was formed. As the hydrogen pressure increased up to 70 Pa, the relative weight percent of LiBH₄ was over 70 wt.% even at ambient temperature. Moreover, the stress of the films was decreased as the hydrogen pressure increased.     

Amelioration of the hydriding and dehydriding kinetics of Mg by pulverization and the formation of Mg2Ni hydride

The addition of an oxide Fe₂O₃ is considered to increase the hydriding rate of Mg by pulverization, and the addition of Ni to increase the hydriding and dehydriding rates by the formation of Mg₂Ni hydride. The sample Mg-10 wt.% (Fe₂O₃, Ni) was prepared by grinding Mg mechanically under H₂ (reactive mechanical grinding) with nano-structured Fe₂O₃ particles and Ni. The as-milled sample absorbed 4.24 wt.% hydrogen at 593 K under 12 bar H₂ for 60 min. Its activation was accomplished after two hydriding-dehydriding cycles. The activated sample absorbed 4.05 wt.% hydrogen at 593 K, 12 bar H₂ for 60 min and desorbed 3.05 wt.% hydrogen at 593 K, 1.0 bar H₂ for 60 min. After hydriding-dehydriding cycling, Mg₂Ni is formed by the reaction of Mg with Ni, Fe₂O₃ is reduced, and a small fraction of Mg is oxidized.     

Study on the homogeneity of hydrogenation for LaFe11.5Si1.5 intermetallic compound

The homogeneity of hydrogen absorption for LaFe_11.5Si_1.5 intermetallic compound was investigated. The hydrides remained NaZn₁₃-type structure when the hydrogenation temperature varied from 423 K to 923 K under 1 atm hydrogen atmosphere. The Differential Scanning calorimetric (DSC) measurements revealed slightly inhomogeneous distribution of hydrogen atoms in the hydrides hydrogenated at a low temperature. The activation before hydrogenating at a higher temperature could improve the homogeneity of hydrogen absorption. Uniform magnetic transition temperature, corresponding to the homogeneous hydrogen absorption, was observed by hydrogenating the compound at 823 K, or at 523 K after activation. The maximum magnetic entropy change ΔS_M (ΔH = 2 T) for the compound hydrogenated at 823 K is about 15.5 J/kg K with the latent heat of 5.12 × 10³ J/kg during the phase transition.     

Optimization of sputtering parameters for deposition of Al-doped ZnO films by rf magnetron sputtering in Ar + H2 ambient at room temperature

The effects of sputtering pressure and power on structural and optical-electrical properties of Al-doped ZnO films were systemically investigated at substrate temperature of room temperature and H₂/(Ar + H₂) flow ratio of 5%. The results show that carrier concentration and mobility of the films show nonmonotone change due to the evolution of microstructure and lattice defect of the films caused by introduction of H₂ with increasing sputtering pressure and power. The transmittance of the films is also found to be related to the introduction of H₂ in addition to usually considered surface roughness and crystallinity. Finally, optimized sputtering pressure and power are 0.8 Pa and 100 W, respectively, and obtained minimum resistivity and highest transmittance are 1.43 × 10^− 3 Ω·cm and 90.5%, respectively. In addition, it is found that E_g of the films is mainly controlled by the carrier concentration, but crystallite size and stress should also be considered for the films deposited at different powers.     

Controlled synthesis and photoluminescence properties of BaXO4 (X = W, Mo) hierarchical nanostructures via a facile solution route

Shape-controlled synthesis of BaWO₄ hierarchical nanostructures has been achieved in a mixed solvent of water and ethanol at room temperature. By simply adjusting the volume ratio of C₂H₅OH and H₂O (R ratio), the size and shape of BaWO₄ nanostructures, such as shuttle-like and ellipsoid-like, are successfully controlled. This simple method has been extended to synthesize BaMoO₄ hierarchical nanostructures. Both BaWO₄ and BaMoO₄ hierarchical nanostructures exhibited new green emission peaks at 558 and 560 nm, respectively.     

Hydrogen sensing properties of Pd-doped SnO2 sputtered films with columnar nanostructures

Pd-doped SnO₂ sputtered films with columnar nanostructures were deposited using reactive magnetron sputtering at the substrate temperature of 300 °C and the discharge gas pressures of 1.5, 12, and 24 Pa. Structural characterization by means of X-ray diffraction and scanning electron microscopy shows that the films composed of columnar nanograins have a tetragonal SnO₂ structure. The films become porous as the discharge gas pressure increases. Gas sensing measurements demonstrate that the films show reversible response to H₂ gas. The sensitivity increases as the discharge gas pressure increases, and the operating temperature at which the sensitivity shows a maximum is lowered. The highest sensitivity defined by (R_a − R_g) / R_g, where R_a and R_g are the resistances before and after exposure to H₂, 84.3 is obtained for the Pd-doped film deposited at 24 Pa and 300 °C upon exposure to 1000 ppm H₂ gas at the operating temperature of 200 °C. The improved gas sensing properties were attributed to the porosity of columnar nanostructures and catalytic activities of Pd doping.     

Synthesis and selective gas-sensing properties of hierarchically porous intestine-like SnO2 hollow nanostructures

Hierarchically porous intestine-like SnO₂ hollow nanostructures of different dimension were successfully synthesized via a facile, organic template free, H₂O₂-assisted method at room temperature. The morphology as well as texture (congregated solid sphere, intestine-like solid nanostructure, hollow core–shell one, and intestine-like hollow one) of SnO₂ materials can be controlled by varying H₂O₂ concentration and the size of intestine-like hollow SnO₂ can be tuned in the range of 20–120 nm by changing SnSO₄ concentration. The hierarchically porous intestine-like SnO₂ has high specific surface area (142 m² g⁻¹). The gas-sensing behaviors of the intestine-like SnO₂ material to different gas probes such as ethanol, H₂, CO, methane, and butane have been investigated; among them a high selectivity to ethanol was achieved.     

Improved activation and hydrogen storage properties of a Mg85Ni15 melt-spun alloy via surface treatment with NH4 solution

An amorphous Mg₈₅Ni₁₅ melt-spun hydrogen storage alloy, processed by submersion in an aqueous solution of NH₄⁺, is able to absorb nearly 5 mass% hydrogen at 473 K during the first hydrogenation cycle. The nanocrystalline microstructure formed during devitrification of the metallic glass is preserved by the lower required activation temperature of the NH₄⁺-treated material compared to the as-spun material; and the kinetics of subsequent absorption/desorption cycles at 573 K are dramatically improved. The material activated at 473 K exhibits a decrease in hydride decomposition temperature by 30 K, observed via DSC and TPD experiments, compared to a sample activated at 573 K. The NH₄⁺-treatment of a glassy alloy presented here provides a practical alternative to ball milling for forming a nanocrystalline material and facilitating activation, requiring much less time and a more commercially scalable option.     

Synthesis and photoluminescent properties of CaMoO4 nanostructures at room temperature

CaMoO₄ nanostructures with different morphologies, such as ellipsoid-like, spindle-like, and sphere-like, were successfully synthesized in a simple cationic surfactant-CTAB-microemulsion system at room temperature. The molar ratio (w) of H₂O to CTAB and the concentration of reactants played important roles in the morphological control of CaMoO₄ nanostructures. A possible mechanism was proposed for the selective formation of the different morphologies. The CaMoO₄ nanostructures exhibited excellent photoluminescence properties with the same new green emission peaks at 495 nm.     

Hydrogen peroxide-assisted hydrothermal synthesis of hierarchical CuO flower-like nanostructures

Hierarchical CuO nanostructures were synthesized through a hydrogen peroxide-assisted hydrothermal route in which Cu(OH)₂ was the copper source. The CuO nanostructures were composed of numerous nanobelts that radiated from the center of the nanostructure and formed a flower-like shape with a diameter of 5-10 μm. The nanobelts had lengths of 2.5-5 μm and widths of 150-200 nm. The H₂O₂ concentration directly influenced the product morphology. As the concentration of H₂O₂ increased, the length and width of the nanobelts increased and the quantity of the nanobelts decreased. The possible formation mechanism of hierarchical CuO flower-like nanostructures was presented.     

Effect of hot-filament annealing in a hydrogen atmosphere on the electrical and structural properties of Nb-doped TiO2 sputtered thin films

In this work Nb-doped TiO2 thin films were deposited by d.c.-pulsed reactive magnetron sputtering at 500 °C from a composite target with weight fractions of 96% Ti and 4% Nb, using oxygen as reactive gas. In order to enhance the conductive properties, the as-deposited samples were treated in vacuum with atomic hydrogen at a substrate temperature of 500 °C. The atomic hydrogen flow was generated by a hot filament, inside a high-vacuum chemical vapour deposition reactor, at a temperature of 1750 °C. In order to optimise the hydrogen hot-wire treatments, the H₂ pressure was varied between 1.3 and 67 Pa, the treatment time was monitored between 1 and 5 min and the hot-filament current was changed between 12 and 17 A. Dark conductivity was measured as a function of temperature and its value at room temperature was extrapolated and used to assess the effect of the hydrogen annealing on the charge transport properties. A two-order of magnitude increase in dark conductivity was typically observed for optimised hydrogen treatments (10 Pa), when varying the hydrogen pressure, resulting in a minimum resistivity of ~ 3 × 10^− 3 Ω cm at room temperature. The maximum amount of atomic H incorporation in oxygen vacancies was determined to be ~ 5.7 at.%. Carrier mobility and resistivity were also investigated using Hall effect measurements. Correlations between structural and electrical properties and the hydrogen treatment conditions are discussed. The purpose of these films is to provide a transparent and conductive front contact layer for a-Si based photovoltaics, with a refractive index that better matches that of single and tandem solar cell structures. This can be achieved by an appropriate incorporation of a very small amount of cationic doping (Nb^5 +) into the titanium dioxide lattice.     

Low-temperature synthesis of BiFeO3 nanoparticles by ethylenediaminetetraacetic acid complexing sol-gel process

This paper reported a novel approach to synthesize pure BiFeO₃ nanoparticles through an ethylenediaminetetraacetic acid complexing sol-gel process at low temperature. The pure BiFeO₃ nanoparticles were attained at much lower temperature as 600 °C by this process, in contrast to above 800 °C for the traditional solid-state sintering process. The SEM results showed that the prepared BiFeO₃ nanoparticles had a better homogeneity and fine grain morphology. The BiFeO₃ nanoparticles show a weak ferromagnetic order at room temperature, which is quite different from the linear M-H relationship in bulk BiFeO₃. The origin of the weak magnetic property in our samples should be attributed to the size-confinement effects of the BiFeO₃ nanostructures.     

Green synthesis of ZnO2 nanoparticles from hydrozincite and hydrogen peroxide at room temperature

A green method based on the reaction between hydrozincite (Zn₅(CO₃)₂(OH)₆) powder and hydrogen peroxide (H₂O₂, 30 wt.%) in aqueous solution at room temperature was developed for the synthesis of ZnO₂ nanoparticles. Results from X-ray diffraction, transmission electron microscopy and Raman demonstrated that the resultant products were pure cubic phase ZnO₂ nanoparticles, whose sizes were in the range of 3.1-4.2 nm. Thermogravimetric analysis indicated that between 180 and 350 °C, the as-synthesized ZnO₂ nanoparticles had a weight loss of about 16.7%, consistent with the theoretical amount (16.4%) of the O₂ released from ZnO₂ decomposition (ZnO₂ = ZnO + 1/2O₂). The present method was green, simple and cost-effective, which should be suitable for large-scale production of multifunctional ZnO₂ nanoparticles.     

Effects of different acetylene/nitrogen ratios on characteristics of carbon coatings on optical fibers prepared by thermal chemical vapor deposition

The effects of C₂H₂/(C₂H₂ + N₂) ratios on the characteristics of carbon coatings on optical fibers prepared by thermal chemical vapor deposition are investigated. The C₂H₂/(C₂H₂ + N₂) ratios are set to 60, 70, 80, 90, and 100%. Additionally, the deposition temperature, working pressure, and mass flow rate are 1003 K, 133 kPa, and 40 sccm, respectively. The deposition rate, microstructure, and electrical resistivity of carbon coatings are measured. The low-temperature surface morphology of carbon-coated optical fibers is elucidated. Experimental results indicate that the deposition rate increases with increasing the C₂H₂/(C₂H₂ + N₂) ratio, and the deposition process is located at a surface controlled regime. As the deposition rate increases, the electrical resistivity of carbon coatings increases, while the ordered degree, nano-crystallite size, and sp² carbon atoms of the carbon coatings decrease. Additionally, the low-temperature surface morphology of the carbon coatings shows that if the carbon coating thickness is not smaller than 289 nm, decreasing the deposition rate is good for producing hermetic optical fiber coatings.     

Nanocrystalline chemically modified CdIn2O4 thick films for H2S gas sensor

CdIn₂O₄ sensor with high sensitivity and excellent selectivity for H₂S gas was synthesized by using sol-gel technique. Structural, electrical and gas sensing properties of doped and undoped CdIn₂O₄ thick films were studied. XRD revealed the single-phase polycrystalline nature of the synthesized CdIn₂O₄ nanomaterials. Since the resistance change of a sensing material is the measure of its response, selectivity and sensitivity was found to be enhanced by doping different concentrations of cobalt in CdIn₂O₄ thick films. The sensor exhibits high response and selectivity toward H₂S for 10 wt.% Co doped CdIn₂O₄ thick films. The current-voltage characteristics of 10 wt.% Co doped CdIn₂O₄ calcined at 650 °C shows one order increase in current with change in the bias voltage at an operating temperature of 200 °C for 1000 ppm H₂S gas.     

Comparison of the optical and structural properties of nickel oxide-based thin films obtained by chemical bath and sputtering

Nickel oxide thin films were prepared using chemical bath deposition and reactive magnetron dc-sputtering. Through the chemical route, Ni(OH)₂ films were deposited with a nano-porous structure providing large specific surface area. Subsequent annealing at 300 °C transformed the films into NiO. These films showed high absorption in the visible range and low crystallinity due to Ni vacancies. Annealing at higher temperatures removes Ni vacancies improving transmittance and crystallinity. Sputtered films were obtained in Ar + O₂ and Ar + H₂ + O₂ atmospheres at different flux ratios. During deposition in the former atmosphere, substrate temperature was 300 °C producing dense polycrystalline films with excellent optical properties. In the hydrogen containing atmosphere, the substrate was at room temperature and polycrystalline films with a dark-yellowish color and expanded lattice were obtained.     

Hydrogen storing and electrical properties of hyperbranched polymers-based nanoporous materials

Hydrogen storage and electrical properties of different hyperbranched polymer systems beside a nanocomposite are studied. The polymers examined are aliphatic hyperbranched poly urea (P-Urea), polyamide amine (PAMAM) and polyamide amine/vanadium oxide (PAMAM/VO_x) nanocomposite. At 80 K and up to 20 bar hydrogen pressure, the hydrogen storage capacity of hyperbranched P-Urea reached 1.6 wt%, 0.9 wt% in case of PAMAM and 0.6 wt% for VO_x. The hydrogen storage capacity significantly enhanced when PAMAM and VO_x form a nanocomposite and increased up to 2 wt%. At 298 K and up to 20 bar, all the samples did not show measurable hydrogen uptake. Electrical properties of the samples are also investigated; the measurements showed complete insulating behavior at hydrogenation measuring temperature. These investigations ensure that the polymer conductivity does not play a role in hydrogen uptake, also hyperbranched polymers are promising materials for hydrogen storage.     

Preparation of flower-like CuO by a simple chemical precipitation method and their application as electrode materials for capacitor

A novel CuO electrode material with flower-like nanostructures was fabricated at a low temperature (80 °C) by a simple chemical precipitation method. Scanning electron microscopy (SEM) results showed that CuO with spherical and flower-like structure can be formed under a weak alkali (C₆H₁₂N₄), and CuO with sheets structure can be obtained under a strong alkali (NaOH). A possible growth mechanism of CuO nanocrystals was discussed. The flower-like CuO electrode exhibited a higher specific capacitance (133.6 Fg⁻¹) and an excellent cycle performance at a high current density of 10 mA/cm². Specific capacitance of flower-like CuO was 405.3% higher than globular CuO (26.44 Fg⁻¹) at 2 mA/cm².     

Hydrogen absorption/desorption properties of Li–Al–N–H composite

Li₃AlH₆ and LiNH₂ at a 1:3 molar ratio were mechanically milled to yield a Li–Al–N–H composite. The hydrogen storage properties of the composite were studied using thermogravimetry, differential scanning calorimetry, mass spectrometry, and X-ray diffraction. Addition of LiNH₂ lowered the decomposition temperature of Li₃AlH₆. The Li–Al–N–H composite began to release hydrogen at around 110 °C, which was 90 °C lower than the initial desorption temperature of Li₃AlH₆. About 7.46 wt% of hydrogen was released from the composite after heating from room temperature to 500 °C. A total hydrogen desorption capacity of 8.15 wt% was obtained after accounting for hydrogen released in the ball-milling process. The resulting dehydrogenated composite absorbed 3.56 wt% of hydrogen at 400 °C under a hydrogen pressure of 110 bar. The hydrogen absorption capacity and kinetic properties of the Li–Al–N–H composite significantly improved when CeF₃ was added to the composite. A maximum hydrogen absorption capacity of 4.8 wt% was reached when the composite was doped with 2 mol% CeF₃.