RESUMO
This work presents the structural and electrical characterization of K2NiF4-type layered perovskites of LaSrAl1-xMgxO4-δ composition to be used as oxide-ion electrolytes for a solid-oxide fuel cell (SOFC). These perovskites were prepared by mechano-chemical synthesis (ball milling), an alternative to traditional synthesis methods such as citrate-nitrates and solid-state reaction. With these methods, two things are avoided: first, the use of nitrate salts, which are more environmentally harmful than oxide precursors, and second, it saves the series of long thermal treatments associated with solid-state reactions. After grinding the precursors, nanometric particles were obtained with a combination of crystalline regions and amorphous regions; this effect was determined by XRD and TEM, showing that Mg has a positive effect on the phase formation by only mechanical synthesis. R2C4: After sintering, it was found by XRD that the sample x = 0.1 only presents the diffraction peaks corresponding to the desired phase, which shows a phase purity greater than 97%, even higher than that of the standard undoped sample. For x = 0.2 and 0.3, there was a segregation of impurities, possibly by the local migration of La and Sr heavy cations; this was determined by SEM and EDS. The electrical characterization of the sintered pellets was carried out by electrochemical impedance spectroscopy, which determined that the incorporation of Mg in the structure improves the ionic conductivity by three orders of magnitude, obtaining conductivities of 1.6 mS/cm at 900 °C for x = 0.2. Although the improvement in conductivity is considerable, many challenges such as densification, the segregation of impurities, and the study of mechanical and thermal properties must be carried out on these materials to endorse them as solid electrolytes in SOFC.
RESUMO
New electrode materials for supercapacitor devices are the primary focus of current research into energy-storage devices. Besides, exact control of the proportions of these new materials while forming electrodes for coin cell supercapacitor devices is very important for the large-scale manufacturing or at industrial scale. Here we report a facile synthesis of CrOOH with ascorbic acid and explore an exact composition with reduced graphene oxide to achieve a highly efficient electrode material for supercapacitor devices. The rGO is synthesized by modified Hummer's method followed by reduction with ascorbic acid, whereas ultrasmall CrOOH nanoparticles result via hydrothermal treatment of the reactants Cr(NO3)3, NaOH, and ascorbic acid at 120 °C for 12 h. The ultrasmall CrOOH nanoparticles show an amorphous phase with particle size range 3-10 nm and a calculated band gap of 3.28 eV. Six different composites are prepared by varying the proportion of CrOOH and rGO materials and further utilized as active electrode materials for fabrication of the coin cell supercapacitor devices. We report the highest specific capacitance for the 70% CrOOH and 30% rGO composite that exhibits a capacitance of 199.8 mF cm-2 with a long cyclic stability up to the tested 10,000 charge/discharge cycles. The proposed supercapacitor device exhibits a high energy and power density of 8.26 Wh kg-1 and 3756.9 W kg-1, respectively, at Ragone Plot, showing the commercial viability of the device.
RESUMO
We describe the structure and properties of [Zn(C6H4N5)N3] n , a new nonporous three-dimensional high-energy metal-organic framework (HE-MOF) with enhanced thermal stability. The compound is synthesized by the hydrothermal method with in situ ligand formation under controlled pH and characterized using single-crystal X-ray diffraction, elemental analysis, and Fourier transform infrared. The measured detonation temperature (T det = 345 °C) and heat of detonation (ΔH det = -0.380 kcal/g) compare well with commercial explosives and other nitrogen-rich HE-MOFs. The velocity and pressure of denotation are 5.96 km/s and 9.56 GPa, respectively. Differential scanning calorimetry analysis shows that the denotation of [Zn(C6H4N5)N3] n occurs via a complex temperature-dependent mechanism.