法拉第效率
阳极
动力学
阴极
化学
化学工程
离子键合
结合能
试剂
氧化还原
碳纤维
电池(电)
容量损失
离子强度
四氢呋喃
材料科学
钠
离子液体
同种类的
无机化学
过程(计算)
工作(物理)
电化学
高分子
纳米技术
离子
化学动力学
化学物理
作者
Haining Chen,Jin Shi,Bohan Zhang,Mengyao Li,Jiayi Li,Yufei Zhao,Z. Huang,Junwei Han,Wei Lv
标识
DOI:10.1002/ange.202519792
摘要
Abstract Hard carbon (HC) is a promising anode for sodium‐ion batteries (SIBs), but coal‐derived HCs often exhibit low reversible capacity and poor initial Coulombic efficiency (ICE) due to irreversible sodium (Na) loss on defective carbons. Presodiation can directly improve ICE, but the imprecise and slow process can lead to under‐ or oversodiation and the formation of thick and unstable byproducts. Here, we propose a high precision and fast presodiation by aryl‐sodium (Ar–Na) compounds dissolved in tetrahydrofuran (THF) with controlled potential and Ar–Na binding energy. Based on the thermodynamic driving force (redox potential) and ionic transfer kinetics (Ar–Na binding strength), a dual‐descriptor design principle for presodiation agent is established. Phenanthrene–sodium (Ph–Na) with a moderate ionic binding energy of − 0.92 eV and a matched redox potential of 0.24 V versus Na⁺/Na enables ∼100% ICE within 60 s and facilitates the formation of an ultrathin inorganic‐rich SEI in the battery that enhances interfacial kinetics and cycling stability. The presodiated HC delivers a reversible capacity of 308.9 mAh g −1 , and paired with a Na 3 V 2 (PO 4 ) 3 (NVP) cathode exhibits 94.8% ICE, 99.2 mAh g −1 discharge capacity, and 82.6% capacity retention after 350 cycles, demonstrating a scalable presodiation strategy for practical SIBs.
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