Search

Two samples of ZnxMn1−xFe2O4 (x = 0, sample A; and x = 0.4, sample B) were synthesized by the hydrothermal method. From complex impedance measurements in the range 100 Hz–2 MHz and for temperatures T between 30 and 130 °C, the barrier energy between localized states ΔErelax was determined for the first time in these samples. For sample B, a single value of ΔErelax was highlighted (0.221 eV), whilst, for sample A, two values were obtained (0.012 eV and 0.283 eV, below 85 °C and above 85 °C, respectively), associated with two zones of different conductivities. Using the Mott's VRH model and the CBH model, we determined for the first time both the bandgap energy barrier (Wm) and the hopping (crossover) frequency (ωh), at various temperatures. The results show that, for sample A, Wm has a maximum equal to 0.72 eV at a temperature between 70 and 80 °C, whilst, for sample B, Wm has a minimum equal to 0.28 eV at a temperature of 60 °C, the results being in good agreement with the temperature dependence of the static conductivity σDC(T) of the samples. By evaluating σDC and eliminating the conduction losses, we identified, using a novel approach, a dielectric relaxation phenomenon in the samples, characterized by the activation energy EA,rel. At various temperatures, we determined EA,rel, which ranged from 0.195 eV to 0.77 eV. These results are important, as understanding these electrical properties is crucial to various applications, especially in technologies where temperature variation is significant. [ABSTRACT FROM AUTHOR]

The synthesis, thermal behavior and electrical properties of a series of undoped and 1% Ga- or Y-doped lanthanum manganite compounds, obtained via the sol–gel technique, are reported. Scanning electron microscopy (SEM/EDX), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) analyses were performed on all synthesized samples. The XRD results confirmed a good crystallinity for all studied samples, and a change in the crystal structure of Ga- or Y-doped lanthanum manganite (Pm-3m space group) was observed compared to the pristine sample (R-3c space group). Thermal analysis highlighted a different behavior of the doped samples compared to the undoped sample, observed by the different mass losses in the analyzed temperature range. For these materials, it is shown for the first time that the static electrical conductivity, σDC, of Ga- or Y-doped LaMnO3 compounds increases compared to the σDC of the pristine sample, and the thermal activation energy of the process of electrical conduction, EA,cond, increases linearly with the temperature for all three studied samples. [ABSTRACT FROM AUTHOR]

LaMnO3 and 1% Pd-, Ag-, or Y-doped perovskite type nanomaterials were prepared by the sol-gel method, followed by heat treatment at a low temperature (600 °C for 6 h). The investigation through X-ray diffraction and FT-IR spectroscopy indicated that all samples were well crystallized, without secondary phases, and that the transition metal doping changed the crystal structure from the R-3c space group for the undoped LaMnO3 to the Pm-3m space group for the doped perovskite compounds. In this research paper, the efficiencies of the perovskite LaMnO3 materials for methyl orange removal were analyzed, wherein the effect of the doping ions and of the pH on the catalytic activity were studied together with a kinetic approach for the LaMnO3 materials at different values of the pH. Moreover, in the catalytic activity, it should be noted that a slightly better performance was obtained for the Ag-doped materials compared to the Y- and Pd-doped perovskite samples. The results presented for the perovskite LaMnO3 nanomaterials reinforce the interest in these multifunctional materials to be used in industrial applications; e.g., in water treatment. [ABSTRACT FROM AUTHOR]

In this research paper, the thermal behaviour of the mixed valence iron oxides Fe3(PO4)2(OH)2 is presented in both air and vacuum atmosphere. The structure, morphology and the magnetic properties of the iron phosphates samples obtained at selected temperatures were carefully investigated. The electrocatalytic properties of synthetic barbosalite Fe3(PO4)2(OH)2 materials for the oxygen and hydrogen evolution reactions (OER and HER) were investigated in a wide pH range, using graphite electrodes modified with different compositions containing the catalyst. The best results were obtained for the compositions with 6 mg barbosalite. During the HER experiments, overpotentials of − 300 and − 350 mV were observed at the current density of − 10 mA cm−2 in strong alkaline and in strong acidic media, respectively. During the OER studies performed in strong acidic solution and in neutral environment, overpotentials of 320 and 690 mV were obtained at the current density of 10 mA cm−2. These findings complement the existing scientific literature relevant to the water splitting domain. Furthermore, the visible light absorption ability of synthetic Fe2+Fe3+2(PO4)2(OH)2 materials was also evaluated. [ABSTRACT FROM AUTHOR]

Present day scientific research is focused on the identification of renewable and clean alternatives to fossil fuels, with hydrogen being a promising energy source that fulfills both requirements. Given this context, the current work investigates the water splitting electrocatalytic properties of two hydrothermally synthesized transition metal oxides: MnO2 and Fe3O4. Electrodes were obtained by modifying graphite substrates with suspensions in ethanol containing the catalytic materials as such or in compositions, and their activity for the O2 and H2 evolution reactions (OER and HER) was studied in alkaline medium. Out of the MnO2-based electrodes, the one modified with the suspension containing 2 mg MnO2, 1 mg Carbon Black and 10 μL Nafion solution displayed an OER overpotential (ηO2) value, at i = 10 mA/cm2, of 0.53 V, while the one manufactured using the suspension with 4 mg MnO2 and 10 μL Nafion solution showed a HER overpotential (ηH2) of 0.427 V (at i = -10 mA/cm2). From the Fe3O4-based electrodes, the one modified with the suspension containing 2 mg Fe3O4 and 2 mg Carbon Black evidenced the highest catalytic activity for both reactions (ηO2 = 0.51 V and ηH2 = 0.43 V). [ABSTRACT FROM AUTHOR]