Modulating ion–dipole interactions in nonflammable phosphonate-based electrolyte for safe and stable sodium-ion pouch cells

Phosphonate-based electrolytes with the merits of low cost and intrinsic nonflammability are promising candidates to realize the safe operation of sodium-ion batteries. However, they generally suffer from poor interfacial chemistry because of the solvent-dominated solvation structure induced by the strong ion-dipole interactions between cations and phosphonate molecules. Herein, we report an electrolyte design strategy that selectively improves the competitive coordination of low-solvating-power molecules, achieving stable interfacial chemistry with a non-flammable, low-cost and fluorine-free electrolyte. By improving the ion-ion interaction between cation and anion, weakly coordinated molecules can enter the Na<sup>+</sup> solvation shell, thereby promoting more adjustable and advantageous interfacial chemistry. As a result, the fluorine-free Prussian blue||hard carbon pouch cell, with a high cathode mass loading of ∼20 mg cm<sup>-2</sup>, reaches a high capacity retention with an energy density of over 221.7 Wh kg<sup>-1</sup> based on electrode mass and 115.1 Wh kg<sup>-1</sup> based on battery mass.

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Publication Details

Journal
National Science Review
Published
2024-12-23
DOI
https://doi.org/10.1093/nsr/nwae466
Citations
40
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
8.35

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article

Modulating ion–dipole interactions in nonflammable phosphonate-based electrolyte for safe and stable sodium-ion pouch cells

Yao-Jie Lei, Wei‐Hong Lai, Shulei Chou, Xin Tan et al.
40 citations
National Science Review
Advancements in Battery Materials
8.35
article

Modulating ion–dipole interactions in nonflammable phosphonate-based electrolyte for safe and stable sodium-ion pouch cells

Yao-Jie Lei, Wei‐Hong Lai, Shulei Chou, Xin Tan, Yingying Dai, S. Li, Zhengkun Xie, Li Li, Lin Li, Weihua Chen, Zhuo Yang, Jian Chen, Zhiqiang Hao, Xunzhu Zhou
article en
40 citations

Abstract

Phosphonate-based electrolytes with the merits of low cost and intrinsic nonflammability are promising candidates to realize the safe operation of sodium-ion batteries. However, they generally suffer from poor interfacial chemistry because of the solvent-dominated solvation structure induced by the strong ion-dipole interactions between cations and phosphonate molecules. Herein, we report an electrolyte design strategy that selectively improves the competitive coordination of low-solvating-power molecules, achieving stable interfacial chemistry with a non-flammable, low-cost and fluorine-free electrolyte. By improving the ion-ion interaction between cation and anion, weakly coordinated molecules can enter the Na<sup>+</sup> solvation shell, thereby promoting more adjustable and advantageous interfacial chemistry. As a result, the fluorine-free Prussian blue||hard carbon pouch cell, with a high cathode mass loading of ∼20 mg cm<sup>-2</sup>, reaches a high capacity retention with an energy density of over 221.7 Wh kg<sup>-1</sup> based on electrode mass and 115.1 Wh kg<sup>-1</sup> based on battery mass.

National Science ReviewVol. 12(3)
Shanghai University (CN), Wenzhou University (CN), University of Wollongong (AU), Fudan University (CN), Zhengzhou University (CN), Zhengzhou University of Science and Technology (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN), South China University of Technology (CN)
National Natural Science Foundation of China, Australian Research Council, Science and Technology Plan Project of Wenzhou, China, High-end Foreign Experts Recruitment Plan of China, Basic Research Project of Wenzhou City, Natural Science Foundation of Zhejiang Province
Affordable and clean energy
Openalex Percentile: Top 2%
Advancements in Battery Materials
8.35
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