Morphology and performance of CoOOH films synthesized via electrochemical oxidation: substrate effects

In the present work, CoOOH films are synthesized from the electrochemical oxidation of α-Co(OH)₂ as precursor. The substrate influences on the material electrochemical properties are studied. The samples are structural and morphologically characterized using techniques of X-ray diffraction (XRD) and scanning electronic microscopy (SEM). The cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy techniques are used for the electrochemical characterization. The films deposited on steel substrate grew in the vertical hexagonal platelet form. Meanwhile, films on Ti plate presented morphology in agglomerated sphere form. After electrochemical oxidation, the film initial morphology is maintained. The films deposited on steel plate have a structure which favors charge storage showing a high specific capacity value (110.92 mA h g^?1) and cyclic stability of 92% after 1000 cycles. Finally, the relaxation time constant value calculated was 5.6 s. This fact is making this material as a possible good candidate for application as electrode material or additive for other materials, in energy storage devices.     

Synthesis of Na<Subscript>2</Subscript>Ti<Subscript>3</Subscript>O<Subscript>7</Subscript> nanoparticles by sonochemical method for solid state electrolyte applications

Na₂Ti₃O₇ ceramic materials have been widely used in sodium-ion battery applications with relative good results; however, there are still several studies that might be carried out in the improvement of the Na₂Ti₃O₇ properties and the overall batteries’ performance. In this direction, we used sonochemical method following a thermal treatment in order to synthetized pure phase Na₂Ti₃O₇ nanopowders. X-ray diffraction characterization revealed that Na₂Ti₃O₇ is the primary phase in nanopowders and ceramic sample; although, a high level of amorphization was observed in the sonicated nanopowder without heat treatment process. Nanopowder-prepared ceramic sample showed a crystallite size of 50 nm after sintering at 900 °C for 1 h. The specific surface area, pore volume, and pore size were obtained from the B.E.T. measurements, being 51 m² g^?1, 0.07 cm³ g^?1, and 55 Å, respectively. The capacitance values of the nanopowder-prepared ceramic sample were in the order of microfarad. The total energy of the system was used to determine relaxation time of the sample (τ ₀ = 31 ms).     

Understanding electrochemical performance of Ni(OH)2 films: a study contributions to energy storage

Journal of Solid State Electrochemistry - Nanostructured Ni(OH)2 was grown on the surface of a Ti plate via electrodeposition method. Analytical methods were employed to characterize the structure,...     

Characterization of nanostructured ceramics prepared by both high energy ball milling and fast firing sintering processes

High-energy ball milling technique was successfully applied to calcinated lead zirconate titanate (PZT 60/40) powders. After 20?h of ball milling, large PZT particles were completely broken down, reducing its initial size in three orders of magnitude. Experimental results show a huge sinterability enhancement of the PZT powders by using this technique, achieving its maximum sintering rate at ～800°C. Relatively low densities (～91%) were achieved in stoichiometric samples, while in 3% lead excess samples sintered at 950°C for 30, 45, 60, 90 and 120?min using a fast firing process and a post-annealing treatment at 800°C for 4 h, densities of ～97% of the theoretical were achieved. PZT nanostructured ceramics prepared under optimized processing conditions (60?h of powder milling, 950°C of sintering temperature, 60?min of sintering time and a post-annealing process at 800°C during 4?h) show high dielectric constant (ε′) values (900) and low dielectric loss (tan?δ) at room temperature and a ferroelectric-paraelectric transition temperature at 375°C.