Ravi Kumar N V

The dielectric behavior of spark plasma sintered SiC(O)/HfCxN1-x nanocomposites synthesized through polymer derived ceramic route was investigated in the frequency range of 1 kHz to 1 MHz at room temperature. The nanostructural features revealed HfCxN1-x nanocrystals encapsulated in a nanometric thin layer of carbon dispersed uniformly in a SiC(O) matrix with segregated free carbon. The nanocomposites exhibited colossal permittivity values in the order of 103 at 1 kHz which reduced to 646 at 1 MHz. The interfacial polarization mechanism existing between complex nanostructural interfaces and the percolation of HfCxN1-x nanocrystals are believed to be responsible for the high permittivity values observed in the measured frequency range. The AC conductivity exemplified a frequency independent behavior at lower frequencies while at higher frequencies, the conductivity exhibited frequency dependence, indicating the existence of hopping type mechanism.

The mesoporous N-doped TiO2/Si-O-C-N ceramic nanocomposites has been revealed to be a potential candidate towards visible light photocatalytic degradation of organic dyes. The polymer-derived ceramic route was implemented to prepare uniformly distributed in-situ crystallized N-doped TiO2 nanocrystals in a mesoporous amorphous siliconoxycarbonitride matrix. This chemical approach assisted by the hard template pathway resulted in a high surface area (186 m2/g) nanocomposite exhibiting predominantly mesoporous structure with an average pore size of 11 nm. The two-step process involved pyrolysis of the polyhydridomethyilsiloxane impregnated in CMK3 (hard template) under argon generating SiOC-C composites and functionalizing it with titanium n-tetrabutoxide to be pyrolyzed under ammonia to form the titled nanocomposite. Interestingly, pyrolysis in a reactive ammonia atmosphere resulted in the incorporation of nitrogen in the titania lattice while decomposing the template. The Si-O-C-N support on which N-doped TiO2 exhibited superior adsorption of organic dye molecules and photocatalytically active in the visible wavelength. The nanoscaled heterojunctions reduced the recombination rate and the presence of superoxide anions/hydroxyl radicals was found to be responsible for the dye degradation.

Different polymorphs of niobium pentoxide (Nb2O5) were synthesized using niobium ethoxide as a precursor by varying the pyrolyzing temperature. The room temperature X-ray diffractograms revealed the irreversible phase evolution from amorphous to pseudohexagonal (823 K) to orthorhombic (1023 K) and to monoclinic crystal structure (1223 K). While phase evolution was also confirmed by thermogravimetry and dilatometry, Raman spectroscopy clearly suggested complete elimination of free carbon in the pyrolysed ceramics. The sintering conditions were optimized to produce a highly dense (>95%) thermodynamically stable monoclinic Nb2O5. The electrical properties of stable monoclinic Nb2O5 sample were thoroughly studied. The monoclinic Nb2O5 was found to have a dielectric constant of around 28 with a dielectric loss of 0.008 at room temperature and at 100 kHz. At low measurement frequencies, an anomalous increase in the effective dielectric permittivity with increasing temperature was observed. Large values of the ε’ are associated with polarization due to the accumulation of free electrons at the grain boundaries. An analysis of the dispersion curves of Nb2O5 revealed that two relaxation processes are responsible for the observed anomalies, and the temperature dependencies of their parameters (dielectric strength, relaxation time and spectrum broadening parameter) were determined. The low-frequency process (relaxation time τ0 ~ 0.45 s), which makes the largest contribution to the dielectric constant, was apparently due to the inhomogeneous conductivity of ceramics. It was revealed that the DC conductivity of ceramics has thermoactivation character with activation energy of about 660 meV and was determined by the oxygen vacancies.

In this work, nanocomposites made of nanosized zirconia crystallized in situ in an amorphous silicon oxycarbo(nitride) (SiOC(N)) matrix have been designed through a precursor route for visible light photocatalytic applications. The relative volume fraction of the starting precursors and the pyrolysis temperatures not only influences the phase fraction of zirconia crystallites but also stabilizes the tetragonal crystal structure of zirconia (t-ZrO2) at room temperature. The presence of carbon in interstitial sites of zirconia and oxygen vacancy defects led to drastic reduction in the band gap (2.2 eV) of the nanocomposite. Apart from being a perfect host avoiding sintering of the active phase and providing mechanical stability, the amorphous matrix also reduces the recombination rate by forming heterojunctions with t-ZrO2. The reduction in band gap as well as the formation of heterojunctions aids in harnessing the visible light for photocatalytic activity.

The pyrolysis (1000◦ C) of a liquid poly(vinylmethyl-co-methyl)silazane modified by tetrakis(dimethylamido)titanium in flowing ammonia, nitrogen and argon followed by the annealing (1000–1800◦ C) of as-pyrolyzed ceramic powders have been investigated in detail. We first provide a comprehensive mechanistic study of the polymer-to-ceramic conversion based on TG experiments coupled with in-situ mass spectrometry and ex-situ solid-state NMR and FTIR spectroscopies of both the chemically modified polymer and the pyrolysis intermediates. The pyrolysis leads to X-ray amorphous materials with chemical bonding and ceramic yields controlled by the nature of the atmosphere. Then, the structural evolution of the amorphous network of ammonia-, nitrogen-and argon-treated ceramics has been studied above 1000◦ C under nitrogen and argon by X-ray diffraction and electron microscopy. HRTEM images coupled with XRD confirm the formation of nanocomposites after annealing at 1400◦ C. Their unique nanostructural feature appears to be the result of both the molecular origin of the materials and the nature of the atmosphere used during pyrolysis. Samples are composed of an amorphous Si-based ceramic matrix in which TiNx Cy nanocrystals (x + y = 1) are homogeneously formed “in situ” in the matrix during the process and evolve toward fully crystallized compounds as TiN/Si3 N4, TiNx Cy (x + y = 1)/SiC and TiC/SiC nanocomposites after annealing to 1800◦ C as a function of the atmosphere.

High-entropy carbides with tunable crystallization and growth have been demonstrated using single-source precursor derived ceramic route. The in situ nanocrystallization of high-entropy carbide phases, (Ta0.2W0.2V0.2Mo0.2Nb0.2)SiδC and (Ta0.167W0.167V0.167Mo0.167Nb0.167Si0.167)C in amorphous Si-based ceramic matrices was achieved by using polysiloxanes and polycarbosilanes as polymer precursors respectively. The results exemplify a prominent role of the architectures of the polymeric precursors in controlling the structural features of these ceramics at various length scales. In particular, it was observed that high-entropy carbides with rock salt and zinc blende crystal structures were formed when polysiloxanes and polycarbosilanes with different backbone structure were used as polymeric precursors respectively. This is attributed to the thermodynamics of nucleation of the carbidic phases in these nanocomposites. Furthermore, the precursor architecture that dictates free carbon content, influenced nanostructural features and porosity in the material. Therefore, engineering such compositionally complex phases is feasible by selecting suitable polymeric precursors.