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dc.contributor.authorDalvi, Anshuman-
dc.date.accessioned2024-01-27T04:21:02Z-
dc.date.available2024-01-27T04:21:02Z-
dc.date.issued2023-01-
dc.identifier.urihttps://www.mdpi.com/2313-0105/9/2/81-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14010-
dc.description.abstractSolvent-free all-solid-state supercapacitors have recently received attention. Despite their highly specific capacitance, they suffer issues related to the solid–solid interface that degrade their performance during prolonged cycling. Here, we propose a novel strategy for improving the electrode–electrolyte interface by introducing a small amount of polymer into the activated carbon-based electrode. An electrode composition of 80AC:8SA:7AB:5[PEO0.95 (LiClO4)0.05]—where AC, SA, and AB stand for activated carbon, sodium alginate binder, and acetylene black, respectively—is optimized. A composite membrane—viz., PEO-LiClO4 reinforced with 38 wt% NASICON structured nano crystallites of Li1.3Al0.3Ti1.7(PO4)3—is used as a solid electrolyte. Incorporating a small amount of salt-in-polymer (95PEO-5 LiClO4) in the electrode matrix leads to a smooth interface formation, thereby improving the performance parameters of the all-solid-state supercapacitors (ASSCs). A typical supercapacitor with a polymer-incorporated electrode exhibits a specific capacitance of ~102 Fg−1 at a discharge current of 1.5 Ag−1 and an operating voltage of 2 V near room temperature. These ASSCs also exhibit relatively better galvanostatic charge–discharge cycling, coulombic efficiency, specific energy, and power in comparison to those based on conventional activated carbon.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.subjectPhysicsen_US
dc.subjectAll-solid-state supercapacitorsen_US
dc.subjectElectrode–electrolyte interfaceen_US
dc.subjectComposite solid polymer electrolyteen_US
dc.subjectSpecific capacitanceen_US
dc.subjectLi+ ion capacitoren_US
dc.titleImproving Interfaces in All-Solid-State Supercapacitors Using Polymer-Added Activated Carbon Electrodesen_US
dc.typeArticleen_US
Appears in Collections:Department of Physics

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