RESUMEN
The untiring endeavour towards green energy is a trending research among the research community. Thermoelectric materials are of vital importance here owing to their emission-free operation. As a righteous candidate, calcium manganate materials are being explored to increase its figure of merit. In this study, the structural, microstructural, electrical transport, and high-temperature thermoelectric measurements of LaxDyxCa1-2xMnO3 {x = 0.025 (L25D25), 0.05 (L50D50), 0.075 (L75D75), and 0.1 (L100D100)} were systematically performed. The structural confirmation of the synthesised sample was validated using X-ray diffraction, which also revealed the orthorhombic (space group: Pnma) crystallisation of co-doped samples with no traces of secondary peaks. A significant increase in the unit cell volume was observed with rare earth substitutions. The morphological studies revealed that the prepared samples were highly dense and the grain size was reduced with rare earth concentration. The substitution of La and Dy enhanced the conductivity values of pristine CMO by two orders of magnitude due to the high concentration of charge carriers and the presence of Mn3+ ions due to rare earth doping. The conductivity increased with rare earth concentrations but diminished for x = 0.1 due to the localization of charges. The Seebeck coefficient values were negative for all the prepared samples, indicating electrons as the predominant carriers over the entire operating range. A minimum κ of 1.8 W m-1 K-1 was achieved for La0.1Dy0.1Ca0.8MnO3 and the maximum value zT obtained was 0.122 at 1070 K for La0.075Dy0.075Ca0.85MnO3.
RESUMEN
This work investigates and reports the effect of ZnO addition on the ferroelectric properties of (K0.5Na0.5)(Nb0.7Ta0.3)O3 (KNNT) ceramics prepared by a solid state reaction method. Though literature is abundant on the study of the effect of ZnO on the sinterability, microstructure and electrical properties of KNN based materials, the effect of ZnO on their ferroelectric properties has seldom been studied in detail, especially in KNNT. In the current study, 2, 4 and 6 wt% of ZnO was added to KNNT ceramics. The XRD results revealed ZnO addition has no effect on the crystal symmetry of KNNT. However, a ZnO secondary phase was found in KNNT ceramics with 4 and 6 wt% ZnO doping. An increase in grain size was observed with increases in the concentration of ZnO, indicating a direct dependence of grain size on the concentration of ZnO in the KNNT matrix. From ferroelectric studies it was observed that a lower electric field was sufficient to get maximum polarization for ZnO doped KNNT samples compared to that of pure KNNT ceramics. A high remnant polarization (P r = 14.0 µC cm-2) and lower coercive field (E c = 5.6 kV cm-1) was obtained for 2 wt% ZnO doped KNNT. These samples showed the least fatigue (0.8%) after 109 cycles in comparison to pure (5%), 4 wt% ZnO doped (24.9%) and 6 wt% ZnO doped (30%) KNNT ceramics. The diminution in P s, P r, and E c was only 26.0%, 26.2% and 18.5%, respectively, with an increase in measurement temperature, which indicates improved thermal stability in 2 wt% ZnO doped KNNT. From the present study the optimum concentration of ZnO in KNNT is identify to be 2.0 wt% and their improved properties in comparison to the pure KNNT ceramics are discussed in detail.
RESUMEN
Many synthesized semiconductor QDs materials are formed using trioctylphosphine oxide (TOPO) but it requires high temperature, is very expensive and is also hydrophobic. Our study deals with selective syntheses of CdSe and core-shell CdSe/ZnS quantum dots (QDs) in aqueous solution by a simple heating and refluxing method. It is more hydrophilic, needs less temperature, is economically viable and is eco-friendly. Bio-ligands, such as thioacetamide, itaconic acid and glutathione, were used as stabilizers for the biosynthesis of QDs. A simplified aqueous route was used to improve the quality of the colloidal nanocrystals. As a result, highly monodisperse, photoluminescent and biocompatible nanoparticles were obtained. The synthesized QDs were characterized by XRD, FTIR, confocal microscopy, ultraviolet (UV) absorption and photoluminescence (PL). The size of synthesized QDs was observed as 5.74 nm and the core-shell shape was confirmed by using XRD and confocal microscopy respectively. The QD nanoparticles showed antibacterial activity against pathogenic bacteria. The QDs could be applied for biological labelling, fluorescence bio-sensing and bio-imaging etc.
RESUMEN
Harvesting energy from surrounding vibrations and developing self-powered portable devices for wireless and mobile electronics have recently become popular. Here the authors demonstrate the synthesis of piezoelectric energy harvesters based on nanotube arrays by a wet chemical route, which requires no sophisticated instruments. The energy harvester gives an output voltage of 400 mV. Harvesting energy from a sinusoidal magnetic field is another interesting phenomenon for which the authors fabricated a magnetoelectric energy harvester based on piezoelectric-magnetostrictive coaxial nanotube arrays. Piezoelectric K0.5Na0.5NbO3 (KNN) is fabricated as the shell and magnetostrictive CoFe2O4 (CFO) as the core of the composite coaxial nanotubes. The delivered voltages are as high as 300 mV at 500 Hz and at a weak ac magnetic field of 100 Oe. Further tailoring of the thickness of the piezoelectric and magnetic layers can enhance the output voltage by several orders. Easy, single-step wet chemical synthesis enhances the industrial upscaling potential of these nanotubes as energy harvesters. In view of the excellent properties reported here, the lead-free piezoelectric component (KNN) in this nanocomposite should be explored for eco-friendly piezoelectric as well as magnetoelectric power generators in nanoelectromechanical systems (NEMS).
