Articles written in Bulletin of Materials Science
Volume 31 Issue 6 November 2008 pp 885-890 Ceramics
A solid-state metathesis approach initiated by microwave energy has been successfully applied for the synthesis of orthovanadates, M3V2O8 (M = Ca, Sr, and Ba). The structural, vibrational, thermal, optical and chemical properties of synthesized powders are determined by powder X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry, magnetic property measurements and diffused reflectance spectra in the UV–VIS range. The direct bandgap of the synthesized materials was found to be 3.55 ± 0.2 eV, 3.75 ± 0.2 eV and 3.57 ± 0.2 eV for Ca3V2O8, Sr3V2O8 and Ba3V2O8, respectively.
Volume 34 Issue 6 October 2011 pp 1219-1222
The electronic and magnetic properties of Co2CrSi is calculated by using full-potential linearized augmented plane wave (FP–LAPW) method based on density functional theory (DFT). Density of states (DOS), magnetic moment and band structures of the system are presented. For the exchange and correlation energy, local spin density approximation (LSDA+U) with the inclusion of Hubbard potential U is used. Our calculation shows indirect bandgap of 0.91 eV in the minority channel of DOS. This is supported by band structures and hence favoured the half metallic ferromagnetic (HMF) nature of the system. The effective magnetic moment of 4.006 𝜇B also supported our conclusion with a near integral value. The DOS of Co and Cr were found to hybridize and was also responsible for the ferromagnetic nature of the system.
Volume 34 Issue 7 December 2011 pp 1483-1489
A polycrystalline sample of Zr-doped barium titanate (BaTiO3) was prepared by conventional solid state reaction method. The effect of Zr (0.15) on the structural and microstructural properties of BaTiO3 was investigated by XRD and SEM. The electrical properties (dielectric, ferroelectric and impedance spectroscopy) were measured in wide range of frequency and temperature. With substitutions of Zr, the structure of BaTiO3 changes from tetragonal to rhombohedral. Lattice parameters were found to increase with substitution. The room temperature dielectric constant increases from ∼ 1675 to ∼ 10586 and peak dielectric constant value increases from ∼ 13626 to ∼ 21023 with diffuse phase transition. Impedance spectroscopy reveals the formation of grain and grain boundary in the material and found to decrease with increase in temperature.
Volume 36 Issue 1 February 2013 pp 107-114
Synthesis of non-collinear (spin canted) ferrites having the formula, CoCd𝑥Fe2−𝑥O4 (𝑥 = 0.0, 0.2, 0.4, 0.6, 0.8 and 1.0), has been carried out using the sol–gel auto combustion method. The ferrite samples show an interesting magnetic transition from Neel to Yafet–Kittel configuration, as the Cd2+ concentration is increased beyond 𝑥 = 0.4. The FT–IR spectra confirm the formation of the metal oxide bond as they exhibit two frequency bands in the range of ∼595 cm-1 and ∼450 cm-1, corresponding to the tetrahedral and the octahedral stretching vibrations of the metal oxide, respectively. The structural evolutions of the nanophase investigated using powder X-ray diffraction (XRD) technique show that the average crystallite size is ∼35 nm. The magnetic studies reveal that the saturation magnetization, 𝑀s, increases up to 𝑥 = 0.4 and decreases when the value of 𝑥 is > 0.4. It is proposed that the incorporation of Cd2+ ion takes place into the tetrahedral sites and up to 𝑥 = 0.4, Neel’s model is followed. But for 𝑥 > 0.4, canting of spins occurs, as explained by Yafet–Kittel (Y–K) model. The d.c. resistivity decreases as a function of temperature, indicating semiconducting nature of the ferrites and the positive value of Seebeck coefficient establishes 𝑝-type conduction behaviour for all the ferrite samples.
Volume 36 Issue 4 August 2013 pp 535-539
Copper telluride (CuTe) nanowires were synthesized electrochemically from aqueous acidic solution of copper (II) sulphate (CuSO4.5H2O) and tellurium oxide (TeO2) on a copper substrate by template-assisted electrodeposition method. The electrodeposition was conducted at 30 °C and the length of nanowires was controlled by adjusting deposition time. Structural characteristics were examined using X-ray diffraction and scanning electron microscope which confirm the formation of CuTe nanowires. Investigation for chemical sensing was carried out using air and chloroform, acetone, ethanol, glycerol, distilled water as liquids having dielectric constants 1, 4.81, 8.93, 21, 24.55, 42.5 and 80.1, respectively. The results unequivocally prove that copper telluride nanowires can be fabricated as chemical sensors with enhanced sensitivity and reliability.
Volume 37 Issue 4 June 2014 pp 889-893
The special behaviour of nanowires with respect to electrical conductivity makes them suitable for sensing application. In this paper, we present a copper–ferrous (CuFe) nanowires based sensor for detection of chemicals. CuFe nanowires were synthesized by template-assisted electrochemical method. By optimizing the deposition parameters, continuous nanowires on a copper substrate were synthesized. The morphological and structural studies of the synthesized CuFe nanowires were carried out using scanning electron microscope (SEM) and X-ray diffraction (XRD). Substrates containing CuFe nanowires were moulded to form a capacitor. Different chemicals were used as dielectric in the capacitor which showed that the capacitance was a nonlinear function of the dielectric constant of fluid unlike the linear relation shown by conventional capacitors. This unique property of the nanowires based capacitors may be utilized for developing fluid sensors with improved sensitivity.
Volume 38 Issue 5 September 2015 pp 1253-1258
In this work, silver nanoparticles (AgNPs) were synthesized biochemically at room temperature using aqueous extract of rhizome of
Volume 38 Issue 5 September 2015 pp 1399-1405
Dielectric analysis of nanometre range size ceramic particles like TiO2 is very important in the understanding of the performance and design of their polymer nanocomposites for energy storage and other applications. In recent times, impedance spectroscopy is shown to be a very powerful tool to investigate the dielectric characteristics of not only sintered and/or pelleted ceramic materials but also particulates/powders (both micron-sized and nano-sized) using the slurry technique. In the present work, impedance spectroscopy employing slurry methodology was extended to study the influence of various chemical groups on the nano-TiO2 surface on the electrical resistivity and the dielectric permittivity of nanoparticles. In this regard, different organophosphate ligands with linear, aromatic and extended aromatic nature of organic groups were employed to remediate the surface effects of nanoTiO2. It was observed that the type of chemical nature of surface engineered nanoparticles’ surface played significant role in controlling the surface electrical resistivity of nanoparticles. Surface passivated nanoTiO2 yielded dielectric permittivity of about 70–80, respectively.
Volume 42 Issue 1 February 2019 Article ID 0033
A high efficiency (>18%) industrial large area crystalline silicon wafer solar cell fabrication process generally requires industrial equipment with large footprint, high capital and running costs. Stricter processing window, continuousmonitoring and automated functioning are the reasons for it. However, for any conventional laboratory (lab) it is always difficult to manage these requirements with limited available lab space or insufficient fund and other related resources. In this work, we report a novel way to fabricate high efficiency full area aluminium back surface field monocrystalline silicon wafer solar cells in our lab using low-cost processing with small-footprint fabrication tools for 6 inch pseudo-square industrial wafers. The novelty of our work includes optimization of every fabrication process step, e.g., texturization, emitter diffusion, emitter passivation and anti-reflection coating deposition, edge-isolation, screen printing and co-firing individually. These modifications include tuning of processing tools and processes, utility changes and inclusion of additional process steps.Beaker-based chemical processes, manual diffusion furnace, introduction of low temperature oxidation, low temperature silicon nitride deposition processes, plasma-edge isolation tool, single manual screen printer, single oven drying of metal pastes and co-firing using rapid thermal processing tools were used at our lab. For our cells, actual and active area efficiencies of 18.5 and 19% (measured under AM1.5G 1 Sun condition), respectively, were achieved.
Volume 42 | Issue 6
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