Electrochemical intercalation of Calcium and Magnesium in TiS2: fundamental studies related to multivalent battery applications

A comparative study of the electrochemical intercalation of Ca2+ and Mg2+ in layered TiS2 using alkylcarbonate-based electrolytes is reported, and for the first time, reversible electrochemical Ca2+ insertion is proved in this compound using both X-ray diffraction and differential absorption X-ray t...

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Detalles Bibliográficos
Autores: Tchitchekova, Deyana S., Ponrouch, Alexandre, Verrelli, Roberta, Broux, Thibault, Frontera, Carlos, Sorrentino, Andrea, Barde, Fanny, Biskup Zaja, Nevenko, Arroyo De Dompablo, María Elena, Palacín, M. Rosa
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/105870
Acceso en línea:https://hdl.handle.net/20.500.14352/105870
Access Level:acceso abierto
Palabra clave:544.6
X-ray microscopy
Rechargeable batteries
Positive electrode
Vanadium-oxide
Ion batteries
Mg batteries
Metal-oxides
Cycle-life
Image
Visualization
Química física (Física)
2210.05 Electroquímica
Descripción
Sumario:A comparative study of the electrochemical intercalation of Ca2+ and Mg2+ in layered TiS2 using alkylcarbonate-based electrolytes is reported, and for the first time, reversible electrochemical Ca2+ insertion is proved in this compound using both X-ray diffraction and differential absorption X-ray tomography at the Ca L-2 edge. Different new phases are formed upon M2+ insertion that are structurally characterized, their amount and composition being dependent on M2+ and the experimental conditions. The first phase formed upon reduction is found to be the result of an ion-solvated intercalation mechanism, with solvent molecule(s) being cointercalated with the M2+ cation. Upon further reduction, new non-cointercalated calcium-containing phases seem to form at the expense of unreacted TiS2. The calculated activation energy barriers for Ca2+ migration in TiS2 (0.75 eV) are lower than those previously reported for Mg (1.14 eV) at the dilute limit and within the CdI2 structural type. DFT results indicate that the expansion of the interlayer space lowers the energy barrier and favors a different pathway for Ca2+ migration.