<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bala, Tanushree</style></author><author><style face="normal" font="default" size="100%">Enoki, Toshiaki</style></author><author><style face="normal" font="default" size="100%">Bhagavatula L. V. Prasad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ferromagnetic resonance in nanomagnetic metal core and noble metal shell systems</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Nanoscience and Nanotechnology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fmr Study; Line Width Comparison; Magnetic Core-Noble Metal Shell Nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">SEP</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">3134-3139</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The change in the line widths in the ferromagnetic resonance (FMR) spectra of Co and Ni nanoparticles upon shell formation with noble metals like gold or silver are described. The NicoreAgshell, CocoreAgshell, and CocoreAushell nanoparticles were prepared by a simple transmetallation reaction between the Co and Ni nanoparticles and the Ag+ or AuCl−4 ions. It is revealed that the FMR line width decreases upon Ag shell formation whereas it increases upon core–shell composite formation with Au. Several probable explanations such as the differences in size distributions before and after the reaction or the changes occurring in shape anisotropy of the particles due to the shell formation or the different extents of electronic interaction between the core and shell materials have been offered for this observation.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">7</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom2><style face="normal" font="default" size="100%">&lt;p&gt;Council of Scientific &amp;amp; Industrial Research (CSIR) - India&lt;/p&gt;</style></custom2><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">1.338</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bala, Tanushree</style></author><author><style face="normal" font="default" size="100%">Sanyal, Ambarish</style></author><author><style face="normal" font="default" size="100%">Pant, Jayashree</style></author><author><style face="normal" font="default" size="100%">Bhagavatula L. V. Prasad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Foam based synthesis of metal carbonates: establishing the role of spatial confinement for obtaining interesting morphologies</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Computational and Theoretical Nanoscience</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAY</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">91-97</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The crystallization of different carbonates namely lead carbonate, cadmium carbonate and strontium carbonate in aqueous foam stabilized by the surfactant sodium dodecyl sulphate (SDS) by a method of cation entrapment is described. Reaction of ammonium carbonate with the respective cations electrostatically entrapped in the foam results in the formation of minerals, possibly in the Plateau border and Plateau junction regions of the foam. The unusual morphology of the crystals obtained from foam based synthetic method as compared to the crystals prepared in aqueous solution shows the utility of the template for the growth of crystals with an unusual morphology due to constrained environment. The materials are well characterized using TEM, SEM, EDAX and FTIR techniques. The large interfacial area of the liquid lamellae in the foam provides a striking possibility for the large-scale synthesis for not only minerals but also other nanoscale materials.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><custom2><style face="normal" font="default" size="100%">&lt;p&gt;Council of Scientific &amp;amp; Industrial Research (CSIR) - India&lt;/p&gt;</style></custom2><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">1.26</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sardar, Debasmita</style></author><author><style face="normal" font="default" size="100%">Neogi, S. K.</style></author><author><style face="normal" font="default" size="100%">Bandyopadhyay, Sanjoy</style></author><author><style face="normal" font="default" size="100%">Satpati, Biswarup</style></author><author><style face="normal" font="default" size="100%">Jain, Ruchi</style></author><author><style face="normal" font="default" size="100%">Gopinath, Chinnakonda S.</style></author><author><style face="normal" font="default" size="100%">Bala, Tanushree</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Facile method for the synthesis of Co-core Au-shell nanohybrid</style></title><secondary-title><style face="normal" font="default" size="100%">New Journal Of Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">SEP</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">9</style></number><publisher><style face="normal" font="default" size="100%">ROYAL SOC CHEMISTRY</style></publisher><pub-location><style face="normal" font="default" size="100%">THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND</style></pub-location><volume><style face="normal" font="default" size="100%">38</style></volume><pages><style face="normal" font="default" size="100%">4107-4114</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Heterostructured Co-Au core-shell nanoparticles have been synthesized by reducing AuCl4- ions on cobalt nanoparticles after a minor but effective modification of cobalt surface by an amine. The core shell morphology is emphatically confirmed by thorough investigation through UV-Vis spectroscopy, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopic analysis (TEM). The chemical composition and topography were determined using STEM-HAADF analysis and EFTEM imaging. Fourier transform infrared (FTIR) spectroscopy confirms the surface modification of Co nanoparticles and the interactions involved between the ligands and the core and shell metals at various steps of the synthetic process. The magnetic properties confirm the material to be superparamagnetic in nature.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">9</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">3.36</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Das, Subhasis</style></author><author><style face="normal" font="default" size="100%">Bordoloi, Ankur</style></author><author><style face="normal" font="default" size="100%">Ghosalya, Manoj Kumar</style></author><author><style face="normal" font="default" size="100%">Gopinath, Chinnakonda S.</style></author><author><style face="normal" font="default" size="100%">Bala, Tanushree</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Facile synthesis of Al2O3-Pt nanocomposite and its catalytic activity</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">NOV</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">Article Number: 115002</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Pt nanoparticles were synthesized on gamma-alumina support in presence of oleic acid which was found to prevent clustering of Pt nanoparticles on the support. Various percentage of Pt loading on the alumina changed the catalytic activity for preferential oxidation of CO at relatively low temperature in H-2 rich stream. Pt nanoparticles when synthesized in absence of oleic acid, were all clustered and did not have any catalytic activity. The presence of oleic acid promoted stability preventing agglomeration of Pt nanoparticles. The catalyst thus prepared was characterized thoroughly and their catalytic activity was studied in details.</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">1.068</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sardar, Debasmita</style></author><author><style face="normal" font="default" size="100%">Maity, Jayeta</style></author><author><style face="normal" font="default" size="100%">Ghosalya, Manoj Kumar</style></author><author><style face="normal" font="default" size="100%">Gopinath, Chinnakonda S.</style></author><author><style face="normal" font="default" size="100%">Bala, Tanushree</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Facile synthesis of ZnO-Ag nanocomposite and its photocatalytic activity</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAY</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">Article Number: 055011</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The evolution of photoactive hybrid materials (e.g. noble metal-semiconductor) has resulted in heterogeneous photocatalysis. We report a facile route for the synthesis of ZnO-Ag nanocomposites with varying percentage of loading of the noble metal, expecting a great boost in the photocatalytic behavior of ZnO. The as prepared material was thoroughly characterized by UV-Vis, FTIR, TEM, FESEM, XRD, XPS analyses. The photocatalytic activities of the nanocomposites have been assessed from the ability to degrade methylene blue dye in aqueous solution. The results suggest that incorporation of Ag nanoparticles on the surface of ZnO particles can enhance catalytic activity in comparison to pure ZnO particles under visible light by minimizing the recombination of photogenerated electron-hole pairs.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;0.968&lt;/p&gt;</style></custom4></record></records></xml>