Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3517
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dc.contributor.authorGAWLI, YOGESHen_US
dc.contributor.authorWAHID, MALIKen_US
dc.contributor.authorFernandes, Rohanen_US
dc.contributor.authorKothari, Dushyanten_US
dc.contributor.authorShelke, Manjushaen_US
dc.contributor.authorOGALE, SATISHCHANDRAen_US
dc.date.accessioned2019-07-01T05:54:54Z
dc.date.available2019-07-01T05:54:54Z
dc.date.issued2017-07en_US
dc.identifier.citationChemistrySelect, 2(20), 5600-5607.en_US
dc.identifier.issn2365-6549en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3517-
dc.identifier.urihttps://doi.org/10.1002/slct.201700909en_US
dc.description.abstractWe show that high‐temperature annealing of a dried hexaphosphate, namely phytic acid, renders activated (micro‐porous) and phosphorus‐functionalized graphene like carbon in a one‐step process. At high enough temperature few volatile phosphates serve as porogen‐forming entities while other groups reactively functionalize the carbon surface. The optimized material has high effective surface area due to the presence of defect states. As an anode material for Li‐ion battery, it exhibits a reversible capacity that is double that of the graphite and is stable for 1000 cycles even at a high current of 5 A g−1. This result is attributed to the concurrent presence of micropores and phosphorus containing groups in the carbon matrix.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectHexaphosphate-Deriveden_US
dc.subjectPhosphorus-Functionalizeden_US
dc.subjectLithium-Ion Battery Anodeen_US
dc.subjectCarbon matrixen_US
dc.subjectLi-ion batteryen_US
dc.subject2017en_US
dc.titleHexaphosphate‐Derived Phosphorus‐Functionalized Carbon for Lithium‐Ion Battery Anodeen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Physicsen_US
dc.identifier.sourcetitleChemistrySelecten_US
dc.publication.originofpublisherForeignen_US
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