Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/36792
Registro completo de metadatos
Campo DC Valor Lengua/Idioma
dc.contributor.authorMena Palacios, Maycol Francisco-
dc.contributor.authorVásquez Arroyave, Ferley Alejandro-
dc.contributor.authorRosero Navarro, Nataly Carolina-
dc.contributor.authorCalderón Gutiérrez, Jorge Andrés-
dc.contributor.conferencenameThe 4th World Conference on Solid Electrolytes for Advanced Applications: Garnets and Competitors (4 : del 4 al 7 de septiembre de 2023 : Clarion Hotel The Edge, Tromso, Noruega)spa
dc.date.accessioned2023-10-04T15:31:19Z-
dc.date.available2023-10-04T15:31:19Z-
dc.date.issued2023-09-05-
dc.identifier.urihttps://hdl.handle.net/10495/36792-
dc.description.abstractABSTRACT: All-solid-state Li-ion batteries (ASSB) are one of the future alternatives for electrochemical energy storage, because it improves energy density and safety. The solid electrolyte in the ASSB is a key element to improve the stability and reduce the flammability of lithium batteries [1-3]. Nevertheless, ASSBs industrial and commercial development have some challenges associated with the lower li-ion conductivity of solid electrolytes l.0xl0-4S cm-1 than liquid electrolytes l.0xl0-2S cm-1, as well as high interfacial resistance due to the poor contact and interfacial reactions between the solid electrolyte and active materials. Although the Li0.34La0.51TiO2.94 perovskite (ABO3) shows high chemical stability, high bulk ionic conductivity (l.0xl0-3S cm-1), the total ionic conductivity is lower (1.96x10-3 S cm-1) because of the grain boundary resistance, which reduces the Li+ transport [4]. Doping the B site of the perovskite structure with cations of smaller ionic radius is an alternative to decrease the interatomic bonding forces and improve the lithium conductivity [5]. In this work, we present the synthesis of the material Li0.3La0.57Ti1-xVxO3(x=0-0 .05) using the sol-gel method, thermal treated at 900 °C for 12 hours and sintered at high temperature (1200 °C) for 12 hours, for solid electrolyte of potential use in Li-ion batteries. The physicochemical characterization of the materials was performed by: TGA, DSC, Raman, XRD and SEM coupled to an EDS, while the electrochemical characterization was performed electrochemical impedance spectroscopy and chronoamperometry. The Raman spectra and XRD patterns indicate the perovskite structure formation in the orthorhombic crystal system of all compositions of materials Li0.3La0.57Ti1-xVxO3(x=0-0 .05), showing lower lattice parameters with vanadium doping, which can be attributed to the V+5 substitution, which has an ionic radius (0.54 Å), lower than Ti+5 (0.605 Å) in B cation of perovskite structure. Vanadium-free Li0.3La0.57TiO3 solid electrolyte exhibits the highest total ionic conductivity 4.54xl0-3S cm-1, and Li0.3La0.57Ti0.98V0.02O3 exhibits the high grain conductivity (7.43xl0-4S cm-1). All solid electrolytes exhibit electron conductivities with magnitude l0-8S cm-1 required for the application of solid electrolytes in all-solid batteries.spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rightsAtribución-NoComercial-CompartirIgual 2.5 Colombia*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/*
dc.subject.lcshLithium ion batteries-
dc.subject.lcshBatería de ion de litio-
dc.subject.lcshPerovskita (Mineral)-
dc.subject.lcshPerovskite (Mineral)-
dc.titleLi0.3La0.57Ti1-xVxO3 vanadium doped to improve electrochemical performance as a solid electrolyte in lithium-ion batteriesspa
dc.typeinfo:eu-repo/semantics/conferenceObjectspa
dc.publisher.groupCentro de Investigación Innovación y Desarrollo de Materiales (CIDEMAT)spa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.citationtitleThe 4th World Conference on Solid Electrolytes for Advanced Applications: Garnets and Competitorsspa
oaire.citationconferenceplaceClarion Hotel The Edge, Tromso, Noruegaspa
oaire.citationconferencedate2023-09-04/2023-09-07spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
oaire.fundernameUniversidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIspa
dc.publisher.placeTromso, Noruegaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_6670spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ECspa
dc.type.localPóster de conferenciaspa
dc.subject.lembElectroquímica-
dc.subject.lembElectrochemistry-
dc.subject.lcshurihttp://id.loc.gov/authorities/subjects/sh2011000687-
oaire.awardtitleSENECAspa
dc.description.researchgroupidCOL0007927spa
oaire.awardnumberN° 201926930spa
oaire.funderidentifier.rorRoR:03bp5hc83-
Aparece en las colecciones: Documentos de conferencias en Ingeniería

Ficheros en este ítem:
Fichero Descripción Tamaño Formato  
MaycolMena_2023_lithium-ion batteries.pdfPóster2.9 MBAdobe PDFVisualizar/Abrir
MenaMaycol_2023_lithium-ion batteries.pdfResumen79 kBAdobe PDFVisualizar/Abrir


Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons Creative Commons