Skip to main content
Article

Long‐Life High‐Voltage Sodium‐Ion Batteries Enabled by Electrolytes with Cooperative Na<sup>+</sup>‐Solvation

Yumei LiuBeijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 ChinaYongqing GongSchool of Materials Science and Engineering Tongji University Shanghai 201804 ChinaKe ChenSchool of Materials Science and Engineering Tongji University Shanghai 201804 ChinaLujun ZhuBeijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 ChinaYun AnBeijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 ChinaKenneth I. OzoemenaMolecular Sciences Institute School of Chemistry University of the Witwatersrand Private Bag 3, PO Wits Johannesburg 2050 South AfricaWeibo HuaSchool of Chemical Engineering and Technology Xi'an Jiaotong University No.28, West Xianning Road Xi'an Shaanxi 710049 ChinaMenghao YangSchool of Materials Science and Engineering Tongji University Shanghai 201804 ChinaQuanquan PangBeijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China
2024en
ABI

Abstract

Abstract Stabilizing the electrode interphases is urgently required to enhance the lifetime of high‐voltage sodium‐ion batteries (SIBs). However, the continuous anode solid–electrolyte interphase (SEI) growth associated with electron leakage and the fragile cathode–electrolyte interphase (CEI) lead to capacity fade at high voltage; and yet the solvation‐interphase‐performance relationship is inadequately addressed. Herein, a cooperative Na + ‐solvation strategy is reported to stabilize the interphases by a holistic design of electrolytes combining soft and moderate co‐solvents. The rationally regulated Na + ‐solvation leads to CEI/SEI with the desired thickness and component stability. As such, remarkable cycling stability is achieved for 4.3‐V Na 3 V 2 O 2 (PO 4 ) 2 F (NVOPF) cathodes with 83.3% capacity retention over 3000 cycles at 1 C, significantly outperforming the carbonate counterpart (41.6% capacity retention). Meanwhile, the restrained SEI growth via reducing the formation of electron‐leaking Na 2 CO 3 stabilizes the long‐term cycling of the hard carbon (HC) anode. The assembled NVOPF||HC full cells achieve superior rate capability (up to 15 C) and stable cycling stability over 500 cycles. The demonstrated engineering of electrolyte chemistry, Na + ‐solvation, and interphase structure/component contributes toward the rational establishment of design rules for high‐voltage SIBs and possibly other similar chemistries.

Identifiers

Citations and references

Cited by 20 references