电解质
阳极
阴极
溶剂化
材料科学
硼
电极
电化学
化学工程
钠
无机化学
分析化学(期刊)
离子
化学
冶金
色谱法
有机化学
物理化学
工程类
作者
Yilong Lin,Xiaojing Jin,Shuqing Gao,Feng Liu,Sheng Huang,Xuerui Yang,Yanwu Chen,Yuezhong Meng
标识
DOI:10.1002/chem.202303741
摘要
Abstract Compared with Li + , Na + with a smaller stokes radius has faster de‐solvation kinetics. An electrolyte with ultralow sodium salt (0.3 M NaPF 6 ) is used to reduce the cell cost. However, the organic‐dominated interface, mainly derived from decomposed solvents (SSIP solvation structure), is defective for the long cycling performance of sodium ion batteries. In this work, the simple application of dual additives, including sodium difluoro(oxalato)borate (NaDFOB) and tris(trimethylsilyl)borate (TMSB), is demonstrated to improve the cycling performance of the hard carbon/NaNi 1/3 Fe 1/3 Mn 1/3 O 2 cell by constructing interface films on the anode and cathode. A significant improvement on cycling stability has been achieved by incorporating dual additives of NaDFOB and TMSB. Particularly, the capacity retention increased from 17 % (baseline) to 79 % (w/w, 2.0 wt % NaDFOB) and 83 % (w/w, 2.0 wt % NaDFOB and 1.0 wt % TMSB) after 200 cycles at room temperature. Insight into the mechanism of improved interfacial properties between electrodes and electrolyte in ultralow concentration electrolyte has been investigated through a combination of theoretical computation and experimental techniques.
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