Layered double hydroxide (LDH)-monodispersed 4-nm CdSe nanoparticle composites were prepared through restacking of layers of colloidally dispersed delaminated LDH in the presence of CdSe nanoparticles in 1-butanol. The composites exhibit a blue shift for CdSe absorption, which increases with a decrease in nanoparticle content. The observed blue shift is due to the interaction of the quantum dots with the LDH layers, which leads to surface modification of the nanoparticles.

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This paper presents the joint effect of strain-and doping-induced band gap change in Sn 1Àx Mn x O (0 # x # 0.05) nanoparticles. In addition, an effort was made to understand the effect of Mn doping on the structural and optical properties of SnO 2 . X-ray diffraction analysis showed a tetragonal structure and the unit cell volume decreased slightly with Mn 4+ content. The Mn:SnO 2 are spherical shaped particles with a size ranging from 7.7 to 13.8 nm as calculated by transmission electron microscopy, Scherrer's formula and Willamson-Hall plot. X-ray photoelectron spectroscopy showed clear evidence for tetragonal coordinated high-spin Mn 4+ ions occupying the lattice sites of Sn 4+ in the SnO 2 host. Electron energy loss spectroscopy further confirmed composition and oxidation states of Sn 4+ and Mn 4+ ions. Manganese doping increased the band gap of SnO 2 from 4 eV to 4.40 eV with Mn 4+ concentration. Variation in band gap energy was attributed to the increasing lattice strain with Mn content and the charge transfer transitions between Mn 4+ ions and conduction/valence bands of SnO 2 . Three photoluminescence emission bands observed at 320, 360 and 380 nm, when excited at 250 nm, proved Mn:SnO 2 to exhibit good optical emission and to have potential application in nanoscale optoelectronic devices.

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A B S T R A C TElectron energy loss spectroscopy (EELS) in combination with transmission electron microscopy (TEM) is widely used for chemical state analysis of variety of chemical compounds. High beam sensitivity of substances like polymers hinders the possibility of exploring in-depth analysis provided through the high spatially resolved EELS spectroscopy. In this study, the electron beam irradiation damage on polymers were analyzed with varying dose of electron beams. The stability of the polymers under electron beam exposure depends on the chemical structure on the polymers. In this study the polymers with and without phenyl groups namely Polycarbonate, Polyethylene terephthalate, Polystyrene, Styrene Maleic Anhydride and Polymethylmethacrylate are selected for the comparative degradation study. Effect of varying the electron dose on the stability of polymers were monitored by recording the low-loss EELS spectrum in π to π* transition and (π+σ) to (π+σ)* transition region.

Transition metal oxide (TiO 2 , Fe 2 O 3 , CoO) loaded MCM-41 and MCM-48 were synthesized by a two-step surfactant-based process. Nanoporous, high surface area compounds were obtained after calcination of the compounds. The catalysts were characterized by SEM, XRD, XPS, UV-vis and BET surface area analysis. The catalysts showed high activity for the photocatalytic degradation of both anionic and cationic dyes. The degradation of the dyes was described using Langmuir-Hinshelwood kinetics and the associated rate parameters were determined.