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dc.contributor.authorKandathil, V-
dc.contributor.authorVeetil, A K-
dc.contributor.authorPatra, A-
dc.contributor.authorMoolakkil, A-
dc.contributor.authorKempasiddaiah, M-
dc.contributor.authorSomappa, S B-
dc.contributor.authorRout, C S-
dc.contributor.authorPatil, S A-
dc.date.accessioned2022-02-03T05:29:54Z-
dc.date.available2022-02-03T05:29:54Z-
dc.date.issued2021-09-
dc.identifier.citationJournal of Nanostructure in Chemistry;11(3):395-407en_US
dc.identifier.urihttps://doi.org/10.1007/s40097-020-00375-5-
dc.identifier.urihttp://hdl.handle.net/123456789/3976-
dc.description.abstractA straightforward and facile synthesis of cellulosic-carbon-shielded palladium–magnetic nanoparticle hybrid material (Pd-MNP@SCB) is presented here. Naturally abundant cellulose was isolated from waste sugarcane bagasse via simple base hydrolysis method and employed. Large surface area and porosity are crucial factors which can enhance the efficiency of a material in catalysis as well as energy storage application and the same was tried to achieve here using the cellulosic-carbon as a support. The prepared hybrid material was initially screened for its catalytic activity in Suzuki–Miyaura cross-coupling followed by its utilization in energy storage application. Pd-MNP@SCB could catalyze the cross-coupling reaction very efficiently with excellent functional group tolerance and good recyclability. The electrochemical performance was explored for Pd-MNP@SCB assembled in a two-electrode cell configuration. The maximum capacitance was found to be 121.74 F/g at a current density of 0.07 A/g with an excellent cycling stability of 97.69% over 3000 cycles.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectcelluloseen_US
dc.subjectcarbonen_US
dc.subjectmagnetic nanoparticleen_US
dc.subjectpalladium nanoparticleen_US
dc.subjectenergy storageen_US
dc.subjectSuzuki–Miyaura cross-couplingen_US
dc.titleA Green and Sustainable Cellulosic-Carbon-Shielded Pd–MNP Hybrid Material for Catalysis and Energy Storage Applicationsen_US
dc.typeArticleen_US
Appears in Collections:2021

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