In this study, four different kinds of perovskite powders (LaMnO3, LaFeO3, LaCrO3, and LaNiO3) were prepared and investigated as anode materials for supercapacitor. The as-prepared powders were blended with active carbon and subsequently coated on the nickel plates as the collector layer of the supercapacitors. Three different types of the aqueous solutions (3 M KCl, 1 M LiOH, and 3 M LiOH) were respectively served as the electrolytes for the supercapacitor. The morphology and crystalline phase were characterized by transmission electron microscopy and XRD. The electrical capacity and impedance were measured by the electrochemical capacitance voltage analyzer and impedance spectroscopy. The profiles of specific capacitance of the four different anodic electrodes and three different electrolytes were implemented. The impedance results indicated that four asymmetric pseudocapacitors didnât show any Warburg-type line and semi-circle line in the low-frequency region. According to the CV profiles, the intrinsic LaNiO3 exhibits the highest specific capacitance of 106.58 F/g in 3 M LiOH. Furthermore, the 98% of the initial capacitance of LaNiO3 was retained after 500 charge-discharge life cycles at the maximum current density of 1 A/g. The efficient charge storage of LaNiO3 was attributed by the anion intercalated redox reactions along with the suitability of electrode-electrolyte interactions. Keywords: Perovskite, Lanthanum nickel oxide, Pseudocapacitance, Asymmetric supercapacitor, Oxygen de-intercalatio

Previous synthesis routes created apatites in low crystallinity and high crystallinity states, but a wider range will extend the design capabilities of apatites for hard tissue replacements. While high crystallinity apatites are more conventional, this work investigated lower crystallinity variations from an amorphous state to low crystallinity apatite. Carbonated hydroxyapatite was prepared by precipitating an amorphous phase followed by crystallization at 650 °C at slow (5 °C min⁻¹) and fast heating rates (60 °C min⁻¹). The effect of processing conditions on crystallinity and structural changes was evaluated by thermal analysis, X-ray diffraction, transmission electron microscopy, Fourier transform infrared and Raman spectroscopy. Furthermore, peak deconvolution of IR and Raman spectra resolved the carbonate and phosphate bands and revealed the carbonate and crystalline phase content in CHAp. Similar to precipitation of crystalline apatites, the crystallization at elevated temperature led to carbonate in both the phosphate and hydroxyl positions. Heating at 650 °C provided a nanosized spherical hydroxyapatite containing carbonate controlled by the heating rate. This creates a mechanism for creating a large range in crystallinity with a greater resorption capability for regenerative medicine.

Semiconductor materials have been shown to have good photocatalytic behavior and can be utilized for the photodegradation of organic pollutants. In this work, three-dimensional flower-like SnS₂ (tin sulfide) was synthesized by a facile hydrothermal method. Core-shell structured SiO₂@α-Fe₂O₃ nanocomposites were then deposited on the top of the SnS₂ flowers. The as-synthesized nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV–Vis Spectroscopy, Brunauer–Emmett–Teller (BET) surface area analysis, and photoluminescence (PL) spectroscopy. The photocatalytic behavior of the SnS₂-SiO₂@α-Fe₂O₃ nanocomposites was investigated by observing the degradation of methylene blue (MB). The results show an effective enhancement of photocatalytic activity for the degradation of MB especially for the 15 wt % SiO₂@α-Fe₂O₃ nanocomposites on SnS₂ flowers.

In the present work, we demonstrate the fabrication of laccase biosensor to detect the catechol (CC) using laccase immobilized on graphene-cellulose microfibers (GR-CMF) composite modified screen printed carbon electrode (SPCE). The direct electrochemical behavior of laccase was investigated using laccase immobilized different modified SPCEs, such as GR/SPCE, CMF/SPCE and GR-CMF/SPCE. Compared with laccase immobilized GR and CMF modified SPCEs, a well-defined redox couple of Cu^I/Cu^IIfor laccase was observed at laccase immobilized GR-CMF composite modified SPCE. Cyclic voltammetry results show that the as-prepared biosensor has 7 folds higher catalytic activity with lower oxidation potential towards CC than SPCE modified with GR-CMF composite. Under optimized conditions, amperometrici-tmethod was used for the quantification of CC, and the amperometric response of the biosensor was linear over the concertation of CC ranging from 0.2 to 209.7 μM. The sensitivity, response time and the detection limit of the biosensor for CC is 0.932 μMμA⁻¹cm⁻², 2 s and 0.085 μM, respectively. The biosensor has high selectivity towards CC in the presence of potentially active biomolecules and phenolic compounds. The biosensor also accessed for the detection of CC in different water samples and shows good practicality with an appropriate repea.