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用于超高速钠离子电池的电极-电解质界面化学调制

Electrode-Electrolyte Interfacial Chemistry Modulation for Ultra-High Rate Sodium-Ion Batteries.

作者信息

Tang Zheng, Wang Hong, Wu Peng-Fei, Zhou Si-Yu, Huang Yuan-Cheng, Zhang Rui, Sun Dan, Tang You-Gen, Wang Hai-Yan

机构信息

Hunan Provincial Key Laboratory of Chemical Power Sources, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, P. R China.

出版信息

Angew Chem Int Ed Engl. 2022 Apr 25;61(18):e202200475. doi: 10.1002/anie.202200475. Epub 2022 Mar 9.

Abstract

Sodium-ion batteries capable of operating at rate and temperature extremes are highly desirable, but elusive due to the dynamics and thermodynamics limitations. Herein, a strategy of electrode-electrolyte interfacial chemistry modulation is proposed. The commercial hard carbon demonstrates superior rate performance with 212 mAh g at an ultra-high current density of 5 A g in the electrolyte with weak ion solvation/desolvation, which is much higher than those in common electrolytes (nearly no capacity in carbonate-based electrolytes). Even at -20 °C, a high capacity of 175 mAh g (74 % of its room-temperature capacity) can be maintained at 2 A g . Such an electrode retains 90 % of its initial capacity after 1000 cycles. As proven, weak ion solvation/desolvation of tetrahydrofuran greatly facilitates fast-ion diffusion at the SEI/electrolyte interface and homogeneous SEI with well-distributed NaF and organic components ensures fast Na diffusion through the SEI layer and a stable interface.

摘要

能够在极端速率和温度下运行的钠离子电池非常理想,但由于动力学和热力学限制而难以实现。在此,提出了一种电极-电解质界面化学调制策略。商用硬碳在具有弱离子溶剂化/去溶剂化作用的电解质中,于5 A g的超高电流密度下展现出212 mAh g的优异倍率性能,这远高于普通电解质中的倍率性能(在碳酸盐基电解质中几乎没有容量)。即使在-20°C时,在2 A g的电流密度下仍可保持175 mAh g的高容量(为其室温容量的74%)。这样的电极在1000次循环后仍保留其初始容量的90%。事实证明,四氢呋喃的弱离子溶剂化/去溶剂化极大地促进了SEI/电解质界面处的快速离子扩散,且具有均匀分布的NaF和有机成分的均匀SEI确保了Na通过SEI层的快速扩散以及稳定的界面。

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