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High Na + conducting Na 3 Zr 2 Si 2 PO 12 /Na 2 Si 2 O 5 composites as solid electrolytes for Na + batteries

Sodium superionic conductor Na 3 Zr 2 Si 2 PO 12 (NZSP) is a promising material as a solid electrolyte for sodium‐ion batteries. The highest conductivity of ∼1.0 mS/cm at room temperature (RT) was reported for the compound with a Na content of approximately 3.3 per formula unit (f. u.) and when the...

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Bibliographic Details
Published in:Journal of the American Ceramic Society 2022-07, Vol.105 (7), p.5011-5019
Main Authors: Santhoshkumar, Bandaru, Choudhary, Mahendra Birmaram, Bera, Anup Kumar, Yusuf, Seikh Mohammad, Ghosh, Manasi, Pahari, Bholanath
Format: Article
Language:English
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Summary:Sodium superionic conductor Na 3 Zr 2 Si 2 PO 12 (NZSP) is a promising material as a solid electrolyte for sodium‐ion batteries. The highest conductivity of ∼1.0 mS/cm at room temperature (RT) was reported for the compound with a Na content of approximately 3.3 per formula unit (f. u.) and when the material is synthesized with a final sintering temperature ≥1220°C. Herein, we propose a new synthesis method to enhance the conductivity of the NZSP by liquid‐phase sintering with the optimum amount of additive of amorphous‐Na 2 Si 2 O 5 . In this regard, a series of composite materials were prepared by mixing Na 3 Zr 2 Si 2 PO 12 with amorphous‐Na 2 Si 2 O 5 (NZSP/NS‐ x wt.%; with x  = 0.0, 2.5, 5.0, 7.5, 10.0) and sintering at a lower temperature of 1150°C. Enhanced conductivity of 1.7 mS/cm at RT has been achieved for the Na 3 Zr 2 Si 2 PO 12 /Na 2 Si 2 O 5 ‐5.0 wt.% (NZSP/NS‐5.0) composite. The effects of additives on the NZSP phase formation, microstructure, and ion conductivity have been investigated by XRD, MAS NMR, SEM, and impedance spectroscopy. Our study demonstrates that the higher conductivity of the NZSP/NS‐5.0 composite is caused by the combined effect of increased Na content in the NZSP phase (by diffusion of Na + ions from the liquid phase of NS to bare NZSP phase), higher density, and microstructures with lesser pores.
ISSN:0002-7820
1551-2916
DOI:10.1111/jace.18463