Stable Cycling of Sodium All‐Solid‐State Batteries with High‐Capacity Cathode Presodiation

Abstract Sodium all‐solid‐state batteries (NaSSBs) with an alloy‐type anode (e.g., Sn and Sb) offer superior capacity and energy density compared to hard carbon anode. However, the irreversible loss of Na + at the alloy anode during the initial cycle results in diminished capacity and stability, impairing full‐cell performance. This study presents an easy‐to‐implement cathode presodiation strategy by employing a Na‐rich material to address these challenges. Leveraging the high theoretical capacity and suitable voltage window, Na 2 S is chosen as the Na donor, which is activated by creating a mixed electron‐ion conducting network, delivering a high capacity of 511.7 mAh g −1 . By adding a small amount (i.e., 3 wt.%) of Na 2 S to the cathode composite, a NaCrO 2 || Sn full cell demonstrated capacity improvement from 90.8 to 118.2 mAh g −1 (based on cathode mass). The capacity‐balanced full cell can thus cycle to more than 300 times with >90% capacity retention. This work provides a practical solution to enhance the full‐cell performance and advance the transformation from half‐cell to full‐cell applications of NaSSBs.

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Publication Details

Journal
Advanced Energy Materials
Published
2025-02-16
DOI
https://doi.org/10.1002/aenm.202405678
Citations
4
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
2.92

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article

Stable Cycling of Sodium All‐Solid‐State Batteries with High‐Capacity Cathode Presodiation

Yuju Jeon, Wei Tang, Junlin Wu, Dapeng Xu et al.
4 citations
Advanced Energy Materials
Advancements in Battery Materials
2.92
article

Stable Cycling of Sodium All‐Solid‐State Batteries with High‐Capacity Cathode Presodiation

Yuju Jeon, Wei Tang, Junlin Wu, Dapeng Xu, Dong Ju Lee, Wenjuan Bian, Alexander Fuqua, Zheng Chen, Feng Li
article en
4 citations

Abstract

Abstract Sodium all‐solid‐state batteries (NaSSBs) with an alloy‐type anode (e.g., Sn and Sb) offer superior capacity and energy density compared to hard carbon anode. However, the irreversible loss of Na + at the alloy anode during the initial cycle results in diminished capacity and stability, impairing full‐cell performance. This study presents an easy‐to‐implement cathode presodiation strategy by employing a Na‐rich material to address these challenges. Leveraging the high theoretical capacity and suitable voltage window, Na 2 S is chosen as the Na donor, which is activated by creating a mixed electron‐ion conducting network, delivering a high capacity of 511.7 mAh g −1 . By adding a small amount (i.e., 3 wt.%) of Na 2 S to the cathode composite, a NaCrO 2 || Sn full cell demonstrated capacity improvement from 90.8 to 118.2 mAh g −1 (based on cathode mass). The capacity‐balanced full cell can thus cycle to more than 300 times with >90% capacity retention. This work provides a practical solution to enhance the full‐cell performance and advance the transformation from half‐cell to full‐cell applications of NaSSBs.

Advanced Energy MaterialsVol. 15(23)
Idaho National Laboratory (US), University of California San Diego (US)
National Science Foundation, UC Irvine Materials Research Institute, University of California, San Diego, University of California, Irvine, Division of Materials Research, Division of Electrical, Communications and Cyber Systems, Division of Chemistry
Openalex Percentile: Top 10%
Advancements in Battery Materials
2.92
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