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Reconstructing Helmholtz Plane Enables Robust F‐Rich Interface for Long‐Life and High‐Safe Sodium‐Ion Batteries

Long ChenKey Laboratory of Hydraulic Machinery Transients, Ministry of Education School of Power and Mechanical Engineering Wuhan University Wuhan 430072 P. R. ChinaMing ChenSchool of Energy and Power Engineering Huazhong University of Science & Technology Wuhan 430072 ChinaMing ChenSchool of Energy and Power Engineering Huazhong University of Science & Technology Wuhan 430072 ChinaQingfei MengWuhan Zhongyuan Changjiang Technology Development Co., Ltd. (State No.752 factory) Wuhan 430072 P. R. ChinaJing ZhangWuhan Zhongyuan Changjiang Technology Development Co., Ltd. (State No.752 factory) Wuhan 430072 P. R. ChinaGuang FengSchool of Energy and Power Engineering Huazhong University of Science & Technology Wuhan 430072 ChinaXinping AiHubei Key Laboratory of Electrochemical Power Sources College of Chemistry and Molecular Sciences Wuhan University Wuhan 430072 P. R. ChinaYuliang CaoHubei Key Laboratory of Electrochemical Power Sources College of Chemistry and Molecular Sciences Wuhan University Wuhan 430072 P. R. ChinaZhongxue ChenKey Laboratory of Hydraulic Machinery Transients, Ministry of Education School of Power and Mechanical Engineering Wuhan University Wuhan 430072 P. R. China
2024en
ABI

Annotatsiya

Abstract Hard carbon (HC) is the most commonly used anode material in sodium‐ion batteries. However, the solid‐electrolyte‐interface (SEI) layer formed in carbonate ester‐based electrolytes has an imperceptible dissolution tendency and a sluggish Na + diffusion kinetics, resulting in an unsatisfactory performance of HC anode. Given that electrode/electrolyte interface property is highly dependent on the configuration of Helmholtz plane, we filtrated proper solvents by PFBE (PF 6 − anion binding energy) and CAE (carbon absorption energy) and disclosed the function of chosen TFEP to reconstruct the Helmholtz plane and regulate the SEI film on HC anode. Benefiting from the preferential adsorption tendency on HC surface and strong anion‐dragging interaction of TFEP, a robust and thin anion‐derived F‐rich SEI film is established, which greatly enhances the mechanical stability and the Na + ion diffusion kinetics of the electrode/electrolyte interface. The rationally designed TFEP‐based electrolyte endows Na||HC half‐cell and 2.8 Ah HC||Na 4 Fe 3 (PO 4 ) 2 P 2 O 7 pouch cell with excellent rate capability, long cycle life, high safety and low‐temperature adaptability. It is believed that this insightful recognition of tuning interface properties will pave a new avenue in the design of compatible electrolyte for low‐cost, long‐life, and high‐safe sodium‐ion batteries.

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