NASICON-type Na3VFe(PO4)3 is selected as a cathode material to be coated with a MgO protective film, intended to delay the degradation and improve charge transfer. Replacing vanadium with iron reduces toxicity and enhances sustainability. A scalable procedure is employed to prepare the material with three distinct coating levels (1 %, 3 %, and 5 %), followed by electrochemical testing against a bare reference sample. Unexpectedly, Mg incorporation triggers a phase transition accompanied by an expansion of the unit cell, with Mg preferentially occupying Fe sites. DFT results indicate that the Na3VFe(PO4)3-(001) / MgO interface is thermodynamically stable, and that formation of surface Mg/Fe antisite defects is possible and energetically favorable. Electrochemical tests showed a loss of Fe3+/Fe2+ redox activity at low voltage plateaus, reducing the cell capacity in 3 % and 5 % Mg samples. The charge compensation mechanism exerted by Fe2+/Fe3+ and V3+/V4+/V5+ couples is also confirmed by DFT calculations. The sample containing 1 % Mg delivers the highest capacity at high rates and retains capacity better than the bare sample after extended cycling. The improved electrochemical behavior was confirmed by galvanostatic cycling at −15 °C and 50 °C.

Dual-role magnesium oxide: Enhancing phosphate cathodes for sodium-ion batteries / Lavela, S., Pérez-Vicente, C., Alcántara, R., Lavela, P., Tirado, J.L., Kukeva, R., Stoyanova, R., Di Meglio, V., Massaro, A., Muñoz-García, A.B., Pavone, M.. - In: CHEMICAL ENGINEERING JOURNAL. - ISSN 1385-8947. - 529:(2026). [10.1016/j.cej.2025.172495]

Dual-role magnesium oxide: Enhancing phosphate cathodes for sodium-ion batteries

Di Meglio, Valeria;Massaro, Arianna;Pavone, Michele
2026

Abstract

NASICON-type Na3VFe(PO4)3 is selected as a cathode material to be coated with a MgO protective film, intended to delay the degradation and improve charge transfer. Replacing vanadium with iron reduces toxicity and enhances sustainability. A scalable procedure is employed to prepare the material with three distinct coating levels (1 %, 3 %, and 5 %), followed by electrochemical testing against a bare reference sample. Unexpectedly, Mg incorporation triggers a phase transition accompanied by an expansion of the unit cell, with Mg preferentially occupying Fe sites. DFT results indicate that the Na3VFe(PO4)3-(001) / MgO interface is thermodynamically stable, and that formation of surface Mg/Fe antisite defects is possible and energetically favorable. Electrochemical tests showed a loss of Fe3+/Fe2+ redox activity at low voltage plateaus, reducing the cell capacity in 3 % and 5 % Mg samples. The charge compensation mechanism exerted by Fe2+/Fe3+ and V3+/V4+/V5+ couples is also confirmed by DFT calculations. The sample containing 1 % Mg delivers the highest capacity at high rates and retains capacity better than the bare sample after extended cycling. The improved electrochemical behavior was confirmed by galvanostatic cycling at −15 °C and 50 °C.
2026
Dual-role magnesium oxide: Enhancing phosphate cathodes for sodium-ion batteries / Lavela, S., Pérez-Vicente, C., Alcántara, R., Lavela, P., Tirado, J.L., Kukeva, R., Stoyanova, R., Di Meglio, V., Massaro, A., Muñoz-García, A.B., Pavone, M.. - In: CHEMICAL ENGINEERING JOURNAL. - ISSN 1385-8947. - 529:(2026). [10.1016/j.cej.2025.172495]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/1049279
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