Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/7480
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dc.contributor.authorAhmed, Shadab Alien_US
dc.contributor.authorPareek, Tanvien_US
dc.contributor.authorBadole, Manishen_US
dc.contributor.authorKumar, Sunilen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:11:48Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:11:48Z-
dc.date.issued2020-
dc.identifier.citationAhmed, S. A., Pareek, T., Dwivedi, S., Badole, M., & Kumar, S. (2020). LiSn2(PO4)3-based polymer-in-ceramic composite electrolyte with high ionic conductivity for all-solid-state lithium batteries. Journal of Solid State Electrochemistry, 24(10), 2407-2417. doi:10.1007/s10008-020-04783-zen_US
dc.identifier.issn1432-8488-
dc.identifier.otherEID(2-s2.0-85088457728)-
dc.identifier.urihttps://doi.org/10.1007/s10008-020-04783-z-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/7480-
dc.description.abstractIn this work, fabrication and electrochemical behavior of polymer-in-ceramic composite electrolytes based on lithium-ion conducting triclinic LiSn2(PO4)3 (LSP) for all-solid-state batteries are reported. The composite ceramic electrolyte (CCE) was fabricated using polymeric salt (PEO+LiClO4) as a filler to the ceramic compound LSP using a simple hot-press technique. The x-ray diffraction and Fourier transform infrared spectroscopy (FTIR) studies were performed to determine the structure of the composite electrolyte. Composite electrolyte containing 30 wt.% PEO+LiClO4 exhibit the highest conductivity of ~ 3.48 × 10−5 Scm−1 at 27 °C, which improves to ~ 1.18 × 10−4 Scm−1 at 60 °C. The low activation energy calculated to be ~ 0.34 eV results from additional mobile lithium-ion in a composite electrolyte. The field emission scanning electron microscopy (FESEM) and energy-dispersive x-ray spectroscopy (EDX) reveals the Li+ diffusion route along with the 3D inter-connected LSP-(PEO+LiClO4) interfaces and distribution of polymeric salt to LSP. The ionic and Li+ transference numbers calculated by a combination of ac signal and dc polarization were found to be ~ 0.99 and ~ 0.39, respectively. The electrochemical performance of the CCE was tested using the cyclic voltammetry (CV) and galvanostatic charging-discharging (GCD) in symmetric cell employing lithium metal as the electrode. Composite electrolyte exhibited highly reversible lithium stripping/plating behavior at low current density. All-solid-state cells fabricated using LiMn2O4 as the cathode, Li metal as the anode, and the LSP-30 (PEO+LiClO4) as the solid electrolyte deliver a high specific discharge capacity of ~ 103.3 mAhg−1 at a current density of 100 μAcm−2. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.sourceJournal of Solid State Electrochemistryen_US
dc.subjectActivation energyen_US
dc.subjectCyclic voltammetryen_US
dc.subjectElectric dischargesen_US
dc.subjectEnergy dispersive spectroscopyen_US
dc.subjectField emission cathodesen_US
dc.subjectField emission microscopesen_US
dc.subjectFourier transform infrared spectroscopyen_US
dc.subjectIonic conduction in solidsen_US
dc.subjectLithium metallographyen_US
dc.subjectLithium-ion batteriesen_US
dc.subjectManganese compoundsen_US
dc.subjectPolymersen_US
dc.subjectScanning electron microscopyen_US
dc.subjectSolid state devicesen_US
dc.subjectSolid-State Batteriesen_US
dc.subjectTin compoundsen_US
dc.subjectAll-solid state batteriesen_US
dc.subjectAll-solid-state lithium batteryen_US
dc.subjectComposite electrolytesen_US
dc.subjectElectrochemical behaviorsen_US
dc.subjectElectrochemical performanceen_US
dc.subjectEnergy dispersive X ray spectroscopyen_US
dc.subjectField emission scanning electron microscopyen_US
dc.subjectSpecific discharge capacityen_US
dc.subjectSolid electrolytesen_US
dc.titleLiSn2(PO4)3-based polymer-in-ceramic composite electrolyte with high ionic conductivity for all-solid-state lithium batteriesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Metallurgical Engineering and Materials Sciences

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