<?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%">Usgaonkar, S.</style></author><author><style face="normal" font="default" size="100%">Deshmukh, S.</style></author><author><style face="normal" font="default" size="100%">Biswas, B.</style></author><author><style face="normal" font="default" size="100%">Karjule, N.</style></author><author><style face="normal" font="default" size="100%">Yadav, P.</style></author><author><style face="normal" font="default" size="100%">Nithyanandhan, J.</style></author><author><style face="normal" font="default" size="100%">Kumaraswamy, G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Light-triggered, spatially localized chemistry by photoinduced electron transfer</style></title><secondary-title><style face="normal" font="default" size="100%">Angewandte Chemie-International Edition</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">FEB</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">58</style></volume><pages><style face="normal" font="default" size="100%">2715-2719</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;It is of immense interest to exert spatial and temporal control of chemical reactions. It is now demonstrated that irradiation can trigger reactions specifically at the surface of a simple colloidal construct, obtained by adsorbing polyethyleneimine on fluorescent colloidal particles. Exciting the fluorescent dye in the colloid affords photoinduced electron transfer to spatially proximal amine groups on the adsorbed polymer to form free radical ions. It is demonstrated that these can be harnessed to polymerize acrylic acid monomer at the particle surface, or to break up colloidal assemblies by cleaving a cross‐linked polymer mesh. Formation of free radical ions is not a function of the size of the colloid, neither is it restricted to a specific fluorophore. Fluorophores with redox potentials that allow photoinduced electron transfer with amine groups show formation of free radical ions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">9</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;12.102&lt;/p&gt;
</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%">Yadav, P.</style></author><author><style face="normal" font="default" size="100%">Patrike, A.</style></author><author><style face="normal" font="default" size="100%">Wasnik, K.</style></author><author><style face="normal" font="default" size="100%">Shelke, V.</style></author><author><style face="normal" font="default" size="100%">Shelke, M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Strategies and practical approaches for stable and high energy density sodium-ion battery: a step closer to commercialization</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Today Sustainability</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cathode additives</style></keyword><keyword><style  face="normal" font="default" size="100%">Electrolyte additives</style></keyword><keyword><style  face="normal" font="default" size="100%">Na compensation</style></keyword><keyword><style  face="normal" font="default" size="100%">Self -sacri ficial salts</style></keyword><keyword><style  face="normal" font="default" size="100%">Sodium -ion battery</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUN</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">22</style></volume><pages><style face="normal" font="default" size="100%">100385</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Sodium-ion batteries (SIBs) are reckoned as a potential alternative to Li-ion batteries (LIBs). Currently, the limited supply of precursors and the cost of LIBs have regenerated research and development interest in SIBs. Due to differences in the chemistry of lithium (Li) and sodium (Na), optimized methods for LIBs cannot be blindly applied to develop SIBs. Along with the judicial selection of electrode materials, electrolytes, and interfaces are very crucial for safe, high-power, and long-lasting batteries. The initial part of this review deals with the challenges faced in commercializing SIB full cells. Subsequently, the strategies to improve the energy density of SIB full cells through electrode modifications and electrolyte engineering are described in detail. This review comprehensively represents notable insights into the large-scale commercialization of potential sodium-ion batteries in the full cell.(c) 2023 Elsevier Ltd. All rights reserved.&lt;/p&gt;
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	Foreign&lt;/p&gt;
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	7.244&lt;/p&gt;
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