接口(物质)
亥姆霍兹自由能
离子
钠
平面(几何)
材料科学
计算机科学
化学
物理
几何学
分子
热力学
数学
冶金
有机化学
吉布斯等温线
作者
Long Chen,Ming Chen,Qingfei Meng,Jing Zhang,Guang Feng,Xinping Ai,Yuliang Cao,Zhongxue Chen
标识
DOI:10.1002/ange.202407717
摘要
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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