电化学
无机化学
电解质
水溶液
阴极
锰
氧化物
离子
硝酸钠
化学
锂(药物)
材料科学
化学工程
电极
冶金
有机化学
物理化学
内分泌学
工程类
医学
作者
Munseok S. Chae,Hyojeong J. Kim,Jeyne Lyoo,Ran Attias,Yuval Elias,Yosef Gofer,Seung‐Tae Hong,Doron Aurbach
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2020-11-10
卷期号:3 (11): 10744-10751
被引量:6
标识
DOI:10.1021/acsaem.0c01781
摘要
Aqueous Na-ion batteries are proposed as cheap, safe, environmentally friendly systems for large-scale energy storage owing to the high abundance of sodium in earth's crust and the benign nature of most of its salts. Practical utilization, however, is limited by poor electrochemical performance due to the slow diffusion kinetics of large sodium ions. Here, lithium nitrate was added to the electrolyte solutions to boost the performance of sodium manganese oxide cathodes. Ultrafast rate capability, high ion diffusivity, and superior cycling stability are attributed to enhanced conductivity of the ions in the solution, cointercalation of Li and Na ions, and lower cathode surface resistance. Three-dimensional bond valence maps illuminate the intercalation mechanism of sodium ions in the host structure. Lithium ions establish additional diffusion paths that activate sodium sites. Multistack cells were constructed and showed good electrochemical performance and high mechanical flexibility, which can be exploited to elaborate very effective practical batteries.
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