Li0.3La0.57Ti1-xVxO3 vanadium doped to improve electrochemical performance as a solid electrolyte in lithium-ion batteries
ABSTRACT: 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]....
- Autores:
-
Mena Palacios, Maycol Francisco
Vásquez Arroyave, Ferley Alejandro
Rosero Navarro, Nataly Carolina
Calderón Gutiérrez, Jorge Andrés
- Tipo de recurso:
- http://purl.org/coar/resource_type/c_6670
- Fecha de publicación:
- 2023
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/36792
- Acceso en línea:
- https://hdl.handle.net/10495/36792
- Palabra clave:
- Lithium ion batteries
Batería de ion de litio
Perovskita (Mineral)
Perovskite (Mineral)
Electroquímica
Electrochemistry
http://id.loc.gov/authorities/subjects/sh2011000687
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-sa/4.0/
| Summary: | ABSTRACT: 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. |
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