TiO(2) colloidal nanoparticles and nanocrystals are prepared by hydrolysis of titanium isopropoxide employing a surfactant-free synthetic hydrothermal method. The synthesized samples are characterized by X-ray diffraction (XRD), HRTEM and FTIR. The XRD study confirms that the size of the colloidal nanoparticle is around 4 nm which the HRTEM analysis indicates the sizes of the colloidal nanoparticles are in the range of 2.5 nm. The fluorescence property of the TiO(2) colloidal nanoparticles studied by the emission spectrum confirms the presence of defect levels caused by the oxygen vacancies. We have observed new emission bands at 387 nm,421 nm, 485 nm, 530 nm and 574 nm wavelengths, first one (387 nm) being emission due to annihilation of excitons while remaining four could be arising from surface states. The emission spectrum of annealed nanocrystallites is also having these four band emissions. It is observed that the surface state emission basically consists of two categories of emission.

Optical dating has revolutionized our understanding of Global climate change, Earth surface processes, and human evolution and dispersal over the last ~500 ka. Optical dating is based on an anti-Stokes photon emission generated by electron-hole recombination within quartz or feldspar; it relies, by default, on destructive read-out of the stored chronometric information. We present here a fundamentally new method of optical read-out of the trapped electron population in feldspar. The new signal termed as Infra-Red Photo-Luminescence (IRPL) is a Stokes emission (~1.30 eV) derived from NIR excitation (~1.40 eV) on samples previously exposed to ionizing radiation. Low temperature (7–295 K) spectroscopic and time-resolved investigations suggest that IRPL is generated from excited-to-ground state relaxation within the principal (dosimetry) trap. Since IRPL can be induced even in traps remote from recombination centers, it is likely to contain a stable (non-fading), steady-state component. While IRPL is a powerful tool to understand details of the electron-trapping center, it provides a novel, alternative approach to trapped-charge dating based on direct, non-destructive probing of chronometric information. The possibility of repeated readout of IRPL from individual traps will open opportunities for dating at sub-micron spatial resolution, thus, marking a step change in the optical dating technology.

Process and nanoparticle induced piezoelectric super toughened poly(vinylidene fluoride) (PVDF) nanohybrids have been demonstrated. The nanohybrids have been prepared by incorporating organically modified nanoclay through melt extrusion and solution route. The solution processed nanohybrid exhibit 1100% improvement in toughness as well as adequate stiffness as compared to pure PVDF without any trade-off. The structural and morphological origins of super toughening phenomena have been worked out. The unique crystallization behavior of PVDF on top of the silicate layers (β-phase, planar zigzag chain conformation, and subsequent polar γ-phase and α-phase as layered type) has been revealed to create an island type of structure, which in turn is responsible for greater toughness. The extent of piezoelectric β-phase has been enhanced by controlled stretching of the nanohybrid at moderately high temperature for better disentanglement, and 90% of the piezoelectric phase has been stabilized. The structural change over has been confirmed through XRD, FTIR, and DSC studies. The nanohybrids possess β-phase with a small amount of α-phase and distorted γ-phase (T 3 G-T 6 G) before stretching which convert into predominantly β-phase with increasing the draw ratio, whereas pure PVDF converted directly into β-phase from pure α-phase. The piezoelectric coefficient (d 33 ) exhibits significant increase with draw ratio, and the relative enhancement is more in nanohybrid vis-a-vis pure PVDF arising from the presence of greater β-phase leading to super toughened lightweight piezoelectric material.

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