MnDopant Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> withEnhancedIonic Conductivity for Quasi-Solid-StateSodium–Metal Battery

As a promising solid electrolyte, the NASICON-type Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> holds excellent application in solid-state sodium-ion batteries, which are an alternative to lithium batteries. However, its insufficient conductivity is one of the key factors impeding its applications. Herein, we report Mn<sup>2+</sup>-doped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub>, demonstrating enhanced ionic conductivity and electrochemical properties. We systematically investigate the effect of doping content on the ionic conductivity. The results show that Na<sub>3.4</sub>Zr<sub>1.8</sub>Mn<sub>0.2</sub>Si<sub>2</sub>PO<sub>12</sub> has an extremely high room-temperature ionic conductivity of 3.3 mS cm<sup>–1</sup>, which is 4 times that of undoped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub>. According to the Meyer–Nedle rule, it can be known that as the activation energy decreases, the ionic conductivity shows a gradually increasing trend. Additionally, the Na symmetric batteries using Mn<sup>2+</sup>-doped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> exhibit improved cycling performance. The quasi-solid-state sodium–metal battery using Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> achieves a high discharge specific capacity of 91.3 mAh g<sup>–1</sup> at 0.1C, with a high capacity retention of 92.2% after 260 cycles, far surpassing the counterpart based on undoped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub>. This work provides an effective strategy for enhancing the performance of Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> for its application in sodium–metal batteries.

Publication Details

Journal
Figshare
Published
2025-02-06
DOI
https://doi.org/10.1021/acsami.4c21042.s001
Primary Topic
Advanced Battery Materials and Technologies
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article
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MnDopant Na3Zr2Si2PO12 withEnhancedIonic Conductivity for Quasi-Solid-StateSodium–Metal Battery

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Advanced Battery Materials and Technologies
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MnDopant Na3Zr2Si2PO12 withEnhancedIonic Conductivity for Quasi-Solid-StateSodium–Metal Battery

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Abstract

As a promising solid electrolyte, the NASICON-type Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> holds excellent application in solid-state sodium-ion batteries, which are an alternative to lithium batteries. However, its insufficient conductivity is one of the key factors impeding its applications. Herein, we report Mn<sup>2+</sup>-doped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub>, demonstrating enhanced ionic conductivity and electrochemical properties. We systematically investigate the effect of doping content on the ionic conductivity. The results show that Na<sub>3.4</sub>Zr<sub>1.8</sub>Mn<sub>0.2</sub>Si<sub>2</sub>PO<sub>12</sub> has an extremely high room-temperature ionic conductivity of 3.3 mS cm<sup>–1</sup>, which is 4 times that of undoped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub>. According to the Meyer–Nedle rule, it can be known that as the activation energy decreases, the ionic conductivity shows a gradually increasing trend. Additionally, the Na symmetric batteries using Mn<sup>2+</sup>-doped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> exhibit improved cycling performance. The quasi-solid-state sodium–metal battery using Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> achieves a high discharge specific capacity of 91.3 mAh g<sup>–1</sup> at 0.1C, with a high capacity retention of 92.2% after 260 cycles, far surpassing the counterpart based on undoped Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub>. This work provides an effective strategy for enhancing the performance of Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> for its application in sodium–metal batteries.

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MnDopant Na<sub>3</sub>Zr<sub>2</sub>Si<sub>2</sub>PO<sub>12</sub> withEnhancedIonic Conductivity for Quasi-Solid-StateSodium–Metal Battery · Figshare (2025) | TGRS Research Map | TGRS