02188nas a2200229   4500008004100000022001400041245010800055210006900163260010600232300001400338490000700352520131000359653002501669653001901694653002201713100002001735700001901755700001901774700002001793700001801813856012701831       2008                        eng d  a0025-540800aPhotocatalytic decomposition of methylene nanocrystalline titania prepared by different blue on methods0 aPhotocatalytic decomposition of methylene nanocrystalline titani  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcMAY  a1145-11520 v433 a<p>Nanocrystalline particles of pure anatase titania were prepared by two different methods. One is the sol-gel method at ambient temperature using ultrasonication (TiO2-SG-US) and conventional stirring method (TiO2-SG-S) and the other by surfactant assisted hydrothermal synthesis (TiO2-HT). More uniform distribution/dispersion of the nanoparticles (SEM), marginally higher surface area, better thermal stability and phase purity are some of the advantages of preparation of nanocrystalline titania by sol gel ultrasonication method and hydrothermal synthesis method. The behavior of anatase titania in photocatalytic decomposition of methylene blue in aqueous medium was studied as a function of the method of preparation and the crystallite size. The nanoparticles prepared by ultrasonication method were more effective than both, the sample prepared by conventional stirring method and commercial Degussa P-25. The higher photocatalytic activity of TiO2-SG-US is attributed to the more uniform size of the particles as compared to TiO2-SG-S samples. Both TEM and XRD data on TiO2-HT samples reveal a uniform and nanocrystalline TiO2 particles, which showed photocatalytic activity in both UV and visible region although brookite phase was also present. (C) 2007 Elsevier Ltd. All rights reserved.</p>10aCatalytic properties10aNanostructures10aSol-gel chemistry1 aRamaswamy, Veda1 aJagtap, Neelam1 aVijayanand, S.1 aBhange, Deu, S.1 aAwati, Preeti  uhttp://library.ncl.res.in/content/photocatalytic-decomposition-methylene-nanocrystalline-titania-prepared-different-blue-001910nas a2200253   4500008004100000022001400041245011100055210006900166260007400235300001300309490000700322520098900329653001701318653002401335653001901359653002601378653001901404100001901423700002101442700001901463700001901482700002501501856013001526       2013                        eng d  a0021-891X00aPorous Co3O4 nanorods as superior electrode material for supercapacitors and rechargeable Li-ion batteries0 aPorous Co3O4 nanorods as superior electrode material for superca  aVAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDSbSPRINGERcOCT  a995-10030 v433 a<p>Porous aggregated nanorods of Co3O4 with a surface area of similar to 100 m(2) g(-1) synthesized without using any templates or surfactants give very high specific capacitance of similar to 780 F g(-1) when used as electrode in a faradaic supercapacitor, with a cycle life of more than 1,000 cycles. Further, in Li-ion batteries when used as an anode, the Co3O4 nanorods achieved a capacity of 1155 mA h g(-1) in the first cycle and upon further cycling it is stabilized at 820 mA h g(-1) for more than 25 cycles. Detailed characterization indicated the stability of the material and the improved performance is attributed to the shorter Li-insertion/desertion pathways offered by the highly porous nanostructures. The environmentally benign and easily scalable method of synthesis of the porous Co3O4 nanorods coupled with the superior electrode characteristics in supercapacitors and Li-ion batteries provide efficient energy storage capabilities with promising applications.</p>10aCobalt oxide10aElectrode materials10aLi-ion battery10aPorous nanostructures10asupercapacitor1 aVijayanand, S.1 aKannan, Ramaiyan1 aPotdar, H., S.1 aPillai, V., K.1 aJoy, Pattayil, Alias  uhttp://library.ncl.res.in/content/porous-co3o4-nanorods-superior-electrode-material-supercapacitors-and-rechargeable-li-ion-0