Guardado en:
Detalles Bibliográficos
Autores principales: Pukazhselvan, D., Caha, Ihsan, Loureiro, Francisco J. A., Deepak, Francis Leonard, de Lemos, Catarina, Shaula, Aliaksandr L., Mikhalev, Sergey M., Fagg, Duncan Paul
Formato: Preprint
Publicado: 2026
Materias:
Acceso en línea:https://arxiv.org/abs/2604.25718
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
_version_ 1866917444130439168
author Pukazhselvan, D.
Caha, Ihsan
Loureiro, Francisco J. A.
Deepak, Francis Leonard
de Lemos, Catarina
Shaula, Aliaksandr L.
Mikhalev, Sergey M.
Fagg, Duncan Paul
author_facet Pukazhselvan, D.
Caha, Ihsan
Loureiro, Francisco J. A.
Deepak, Francis Leonard
de Lemos, Catarina
Shaula, Aliaksandr L.
Mikhalev, Sergey M.
Fagg, Duncan Paul
contents This study investigates the lithium conversion behavior of a hydrogen storage material based on vanadium oxide added magnesium hydride. To understand the chemical interaction between vanadium oxide and magnesium hydride, detailed X ray diffraction and X ray photoelectron spectroscopy analyses were performed on ball milled composites with varying compositions. The results confirm the formation of a combined magnesium vanadium oxide with a rock salt structure, indicating strong chemical interaction between the components. It is further shown that the presence of a small amount of this oxide additive significantly influences the lithium reaction with magnesium hydride, leading to a high initial discharge capacity and limited recharge capacity in lithium ion coin cells. Post use analyses confirm the presence of magnesium hydride, suggesting that volume expansion is not responsible for the observed irreversibility. Electrochemical impedance spectroscopy using differential function of relaxation times indicates that electrolyte degradation is not a major issue. Instead, slow charge transfer processes are identified as the limiting factor, and these are sensitive to the composition of the additive. These findings highlight that improving electrode and electrolyte compatibility is essential for enhancing performance in this system.
format Preprint
id arxiv_https___arxiv_org_abs_2604_25718
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Chemical transformation of MgH2/V2O5 composite to Mg-V-O rock salt and its influence on the electrochemical Li conversion and hydrogen storage characteristics of MgH2
Pukazhselvan, D.
Caha, Ihsan
Loureiro, Francisco J. A.
Deepak, Francis Leonard
de Lemos, Catarina
Shaula, Aliaksandr L.
Mikhalev, Sergey M.
Fagg, Duncan Paul
Materials Science
This study investigates the lithium conversion behavior of a hydrogen storage material based on vanadium oxide added magnesium hydride. To understand the chemical interaction between vanadium oxide and magnesium hydride, detailed X ray diffraction and X ray photoelectron spectroscopy analyses were performed on ball milled composites with varying compositions. The results confirm the formation of a combined magnesium vanadium oxide with a rock salt structure, indicating strong chemical interaction between the components. It is further shown that the presence of a small amount of this oxide additive significantly influences the lithium reaction with magnesium hydride, leading to a high initial discharge capacity and limited recharge capacity in lithium ion coin cells. Post use analyses confirm the presence of magnesium hydride, suggesting that volume expansion is not responsible for the observed irreversibility. Electrochemical impedance spectroscopy using differential function of relaxation times indicates that electrolyte degradation is not a major issue. Instead, slow charge transfer processes are identified as the limiting factor, and these are sensitive to the composition of the additive. These findings highlight that improving electrode and electrolyte compatibility is essential for enhancing performance in this system.
title Chemical transformation of MgH2/V2O5 composite to Mg-V-O rock salt and its influence on the electrochemical Li conversion and hydrogen storage characteristics of MgH2
topic Materials Science
url https://arxiv.org/abs/2604.25718