Kripasindhu Sardar

A simple single-source precursor route to the nanostructures of AlN, GaN and InN

In an effort to find a simple and common single-source precursor route for the group 13 metal nitride semiconductor nanostructures, the complexes formed by the trichlorides of Al, Ga and In with urea have been investigated. The complexes, characterized by X-ray crystallography and other techniques, yield the nitrides on thermal decomposition. Single crystalline nanowires of AlN, GaN and InN have been deposited on Si substrates covered with Au islands by using the complexes as precursors. The urea complexes yield single crystalline nanocrystals under solvothermal conditions. The successful synthesis of the nanowires and nanocrystals of these three important nitrides by a simple single-precursor route is noteworthy and the method may indeed be useful in practice.

Phonon Raman scattering of RCrO_{3} perovskites (R=Y, La, Pr, Sm, Gd, Dy, Ho, Yb, Lu)

We report a systematic investigation of orthorhombic perovskite-type RCrO3 powder samples by Raman scattering for nine different rare earth R3+ cations (R = Y, La, Pr, Sm, Gd, Dy, Ho, Yb, and Lu). The room-temperature Raman spectra and the associated phonon mode assignment provide reference data for structural investigation of the whole series of RCrO3 orthochromites and phonon ab-initio calculations. The assignment of the chromite spectra and comparison with Raman data on other orthorhombic perovskites allows correlating the phonon modes with the structural distortions in the RCrO3 series. In particular, two Ag modes are identified as octahedra rotation soft modes, as their positions scale linearly with the octahedra tilt angle of the CrO6 octahedra.

Water-splitting electrocatalysis in acid conditions using ruthenate-iridate pyrochlores

The pyrochlore solid solution (Na0.33Ce0.67)2(Ir1−xRux)2O7 (0≤x≤1), containing B-site RuIV and IrIV is prepared by hydrothermal synthesis and used as a catalyst layer for electrochemical oxygen evolution from water at pH<7. The materials have atomically mixed Ru and Ir and their nanocrystalline form allows effective fabrication of electrode coatings with improved charge densities over a typical (Ru,Ir)O2 catalyst. An in situ study of the catalyst layers using XANES spectroscopy at the Ir LIII and Ru K edges shows that both Ru and Ir participate in redox chemistry at oxygen evolution conditions and that Ru is more active than Ir, being oxidized by almost one oxidation state at maximum applied potential, with no evidence for ruthenate or iridate in +6 or higher oxidation states.

Structural, spectroscopic, magnetic and electrical characterization of Ca-doped polycrystalline bismuth ferrite, Bi1−xCaxFeO3−x/2 (x ≤ 0.1)

The crystal structure and physical properties of multiferroic polycrystalline Ca(2+)-doped BiFeO(3) samples have been investigated. The present experimental investigation suggests that Bi(1-x)Ca(x)FeO(3-x/2) (x ≤ 0.1) can be considered as a solid solution between BiFeO(3) and CaFeO(2.5). The oxidation state of Fe in these materials is + 3 and charge balance occurs through the creation of oxygen vacancies. For each composition, two structural phase transitions are revealed as anomalies in the variable-temperature in situ x-ray diffraction data which is consistent with the well-established high-temperature structural transformation in pure BiFeO(3). All compositions studied show antiferromagnetic behaviour along with a ferromagnetic component that increases with Ca(2+) doping. The resistivities of the Bi(1-x)Ca(x)FeO(3-x/2) samples at room temperature are of the order of 10(9) Ω cm and decrease with increasing Ca(2+) content. Arrhenius plots of the resistivity show two distinct linear regions with activation energies in the range of 0.4-0.7 and 0.03-0.16 eV. A correlation has been established between the critical temperatures associated with the structural phase transitions and the multiferroic properties. A composition of x = 0.085 is predicted to show maximum magneto-electric coupling.

Ferromagnetism in Mn-doped GaN nanocrystals prepared solvothermally at low temperatures

3% and 5% Mn-doped GaN nanocrystals of different sizes, with the average diameters in the range of 4–18nm, have been prepared by two independent routes under solvothermal conditions starting with two different precursors. The reaction temperature was around 350°C in all the preparations. The nanocrystals so prepared exhibit ferromagnetism with magnetization (M) and Curie temperature (TC) values increasing with percent of Mn and particle size. The observation of ferromagnetism in Mn-doped GaN nanocrystals prepared at relatively low temperatures is of significance in understanding this potential in spintronics materials.

Epitaxial GaN films deposited on sapphire substrates prepared by the sol–gel method

Abstract Thin films of GaN have been successfully deposited on Al2O3 (0001) substrates by the sol–gel technique. The method, in addition to being is simple and cost-effective, results in epitaxial films. The films have been characterized by photoluminescence spectroscopy.

Inference of oxygen vacancies in hydrothermal Na0.5Bi0.5TiO3

A high-resolution x-ray powder diffraction study has been made of pseudo-rhombohedral and tetragonal phases in Na0.5Bi0.5TiO3 (NBT), produced via hydrothermal and conventional solidstate methods. Hydrothermal NBT exhibits significantly greater structural distortion at room temperature than solid-state NBT. Peak widths and superstructure peak intensities show a phase transition at 305 C, with trends suggesting that the structure tends towards cubic symmetry at this temperature. Structural refinements indicate that the transition occurs via a phase coexistence region with no clear intermediate phase. Piezoelectric data show evidence of polarisation pinning in hydrothermal NBT, interpreted as a high proportion of oxygen vacancies.

Soft chemical routes to semiconductor nanostructures

Soft chemistry has emerged as an important means of generating nanocrystals, nanowires and other nanostructures of semiconducting materials. We describe the synthesis of CdS and other metal chalcogenide nanocrystals by a solvothermal route. We also describe the synthesis of nanocrystals of AlN, GaN and InN by the reaction of hexamethyldisilazane with the corresponding metal chloride or metal cupferronate under solvothermal conditions. Nanowires of Se and Te have been obtained by a self-seeding solution-based method. A single source precursor based on urea complexes of metal chlorides gives rise to metal nitride nanocrystals, nanowires and nanotubes. The liquidliquid interface provides an excellent medium for preparing single-crystalline films of metal chalcogenides.

Effect of chemical substitution on the Néel temperature of multiferroic Bi1-xCaxFeO3

Multiferroic BiFeO3 ceramics have been doped with Ca. The smaller ionic size of Ca compared with Bi means that doping acts as a proxy for hydrostatic pressure, at a rate of 1%Ca=0.3GPa. It is also found that the magnetic Neel temperature (TNeel) increases as Ca concentration increases, at a rate of 0.66K per 1%Ca (molar). Based on the effect of chemical pressure on TNeel, we argue that applying hydrostatic pressure to pure BiFeO3 can be expected to increase its magnetic transition temperature at a rate around ~2.2K/GPa. The results also suggest that pressure (chemical or hydrostatic) could be used to bring the ferroelectric critical temperature, Tc, and the magnetic TNeel closer together, thereby enhancing magnetoelectric coupling, provided that electrical conductivity can be kept sufficiently low.

Structural variety in iridate oxides and hydroxides from hydrothermal synthesis

We report the results of an exploratory synthetic study of iridium-containing materials using hydrothermal methods from simple metal salts. Three alkali-earth iridium hydroxides are isolated as phase-pure samples and their structures examined by single-crystal or powder diffraction methods: each contains Ir(IV)-centred octahedra, isolated from each other and sharing bridging hydroxides or fluoride with alkali-earth (Ca, Sr or Ba) centres. One of these hydroxides, Ca2IrF(OH)6.OH, possesses a unique open structure, consisting of a positively-charged framework that has one-dimensional channels in which infinite chains of hydrogen-bonded hydroxide anions are encapsulated. The addition of hydrogen peroxide or sodium peroxide to otherwise identical hydrothermal reactions yields dense oxide materials in which iridium is found in an oxidation state between +4 and +5: the novel oxide Na0.8Sr2.2Ir3O10.1 has a KSbO3-type structure with an iridium oxidation state of +5, while the new pyrochlore (Na0.27Ca0.59)2Ir2O6·0.66H2O contains iridium with an average oxidation state close to +4.5. Our results illustrate the utility for hydrothermal synthesis in the discovery of novel complex structures that may be inaccessible using conventional high-temperature synthesis, with control of the metal oxidation state possible with judicious choice of reagents.