Hybrid materials, which consist of organic-inorganic materials, are of profound interest owing to their unexpected synergistically derived properties. These hybrid materials replaced the pristine polymers due to their higher strength and stiffness in the recent years. In the present work, studies concerning the preparation of poly (methyl methacrylate) (PMMA), PMMA/SiO 2 , and PMMA/TiO 2 nanocomposites are reported. These nanocomposite polymers were synthesized by means of free radical polymerization of methyl methacrylate using benzoyl peroxide as an initiator in a water medium. Further 'sol-gel' transformation based hydrolysis and condensation of Ti and Si alkoxides were used to prepare the inorganic phase during the polymerization process of MMA.

No abstract

No abstract

As-deposited sol-gel derived amorphous tungsten oxide films transform into nanostructured films with an interconnected framework of grains and pores and a dominant triclinic crystalline phase upon annealing at 250°C. Transmission electron microscopy and scanning electron microscopy images clearly reveal the annealing-induced microstructural evolution for the film. Subsequent to lithium intercalation, the film annealed at 250°C shows quasi-reversible structural changes, as ascertained by X-ray diffraction and Fourier transform infrared spectral data. Dynamic transmission modulation for film revealed a high optical modulation of 72% ͑ = 650 nm͒ and a coloration efficiency maximum of 132 cm 2 C −1 at 800 nm under a lithium intercalation level of x = 0.20. X-ray photoelectron spectroscopy of the W 4f core levels demonstrated a progressive increase in the W 5+ content at the expense of W 6+ proportion as the insertion coefficient was raised from 0 to 0.25, with 0.20 as the threshold value above which the W 5+ content exceeds the W 6+ proportion. A new W 4+ state also appears which acts to lower the coloration efficiency for x ജ 0.22. The presence of charged oxygen interstitials in the vicinity of electrochemically active tungsten sites is also responsible for the coloration efficiency decline at high ion insertion levels.

A potential driven self-assembly of sodium dodecyl sulfate/tungsten oxide aggregates at the electrolyte-electrode interface followed by template extraction and annealing yielded mesoporous thin films of electrochromic tungsten oxide (WO(3)). Electron microscopy images revealed that the films are characterized by a hitherto unreported hybrid structure comprising nanoparticles and nanorods with a tetragonal crystalline phase of WO(3) with the measured lattice parameters: a = 0.53 nm and c = 0.37 nm. In addition to pentagonal voids characteristic of the tetragonal WO(3) phase at the lattice scale, open channels and pores of 5-10 nm in diameter lie between the nanoparticles, which cumulatively promote rapid charge transport through the film. This resulted in colouration efficiency (η(max)∼90 cm(2) C(-1) at λ = 900 nm) and switching kinetics (colouration time =  3 s and bleaching time =  2 s for a 50% change in transmittance) higher and faster than previously reported values for mesoporous WO(3) films. Repetitive cycling between the clear and blue states has no deleterious effect on the electrochromic performance of the film, which is suggestive of its potential as a cathode in practical electrochromic windows.