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In the present work, cost-effective nanocomposite electrolyte (Ba-SDC) oxide is developed for efficient low-temperature solid oxide fuel cells (LTSOFCs). Analysis has shown that dual phase conduction of O-2 (oxygen ions) and H+ (protons) plays a significant role in the development of advanced LTSOFCs. Comparatively high proton ion conductivity (0.19 s/cm) for LTSOFCs was achieved at low temperature (460 °C). In this article, the ionic conduction behaviour of LTSOFCs is explained by carrying out electrochemical impedance spectroscopy measurements. Further, the phase and structure analysis are investigated by X-ray diffraction and scanning electron microscopy techniques. Finally, we achieved an ionic transport number of the composite electrolyte for LTSOFCs as high as 0.95 and energy and power density of 90% and 550 mW/cm², respectively, after sintering the composite electrolyte at 800 °C for 4 h, which is promising. Our current effort toward the development of an efficient, green, low-temperature solid oxide fuel cell with the incorporation of high proton conductivity composite electrolyte may open frontiers in the fields of energy and fuel cell technology. [ABSTRACT FROM AUTHOR]

Highly dispersive nanospheres of MnFe2O4 are prepared by template free hydrothermal method. The nanospheres have 47.3-nm average diameter, narrow size distribution, and good crystallinity with average crystallite size about 22 nm. The reaction temperature strongly affects the morphology, and high temperature is found to be responsible for growth of uniform nanospheres. Raman spectroscopy reveals high purity of prepared nanospheres. High saturation magnetization (78.3 emu/g), low coercivity (45 Oe, 1 Oe = 79.5775 A·cm−1), low remanence (5.32 emu/g), and high anisotropy constant 2.84 × 104 J/m3 (10 times larger than bulk) are observed at room temperatures. The nearly superparamagnetic behavior is due to comparable size of nanospheres with superparamagnetic critical diameter Dcrspam. The high value of Keff may be due to coupling between the pinned moment in the amorphous shell and the magnetic moment in the core of the nanospheres. The nanospheres show prominent optical absorption in the visible region, and the indirect band gap is estimated to be 0.98 eV from the transmission spectrum. The prepared Mn ferrite has potential applications in biomedicine and photocatalysis. [ABSTRACT FROM AUTHOR]

We have reported new magnetic and optical properties of Mn2O3 nanostructures. The nanostructures have been synthesized by the hydrothermal method combined with the adjustment of pH values in the reaction system. The particular characteristics of the nanostructures have been analyzed by employing X-Ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), Raman spectroscopy (RS), UV-visible spectroscopy, and the vibrating sample magnetometer (VSM). Structural investigation manifests that the synthesized Mn2O3 nanostructures are orthorhombic crystal. Magnetic investigation indicates that the Mn2O3 nanostructures are antiferromagnetic and the antiferromagnetic transition temperature is at TN = 83 K. Furthermore, the Mn2O3 nanostructures possess cantedantiferromagnetic order below the Neel temperature due to spin frustration, resulting in hysteresis with large coercivity (1580 Oe) and remnant magnetization (1.52 emu/g). The UV-visible spectrophotometry was used to determine the transmittance behaviour of Mn2O3 nanostructures. A direct optical band gap of 1.2 eV was acquired by using the Davis-Mott model. The UV-visible spectrum indicates that the absorption is prominent in the visible region, and transparency is more than 80% in the UV region. [ABSTRACT FROM AUTHOR]

Highlights: [•] Substitution of In for Sn in NiCoMnInSn alloys decreases in c/a parameter. [•] Ms of martensite increases and Tc of austenite decreases with In-doping. [•] In-doping shows the strong metamagnetic behavior and magnetocaloric effect. [•] The hysteresis loss is reduced by 74% with increasing the content of In to 8%. [ABSTRACT FROM AUTHOR]

Abstract: We report here the evolution of zinc based high purity phases with novel morphologies such as Zn3N2 hollow structures, ZnO nanowires and nanopowders, as well as metallic Zn layered hexagonal microparticles at progressively increased reaction temperature of 600°C, 700°C, 800°C under NH3 gas atmosphere using Zn powder precursor and keeping all other experimental parameters unchanged. Growth mechanism for Zn3N2 obtained by nitridation, ZnO by oxidation and Zn microparticles via thermal evaporation & condensation process are discussed briefly. The as-synthesized products were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS) and scanning electron microscopy (SEM). Photoluminescence (PL) studies have revealed very interesting and infrequently observed emission bands at 378 and 661nm for Zn3N2, 359 and 396nm for ZnO as well as 389nm for Zn polyhedral microparticles. [Copyright &y& Elsevier]