合金
电极
离子
材料科学
冶金
化学
物理化学
有机化学
作者
Matthew D. L. Garayt,Libin Zhang,Yixiang Zhang,Martins Obialor,Jay Deshmukh,Yingjie Xing,Chongyin Yang,Michael Metzger,J. R. Dahn
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2024-07-01
卷期号:171 (7): 070523-070523
被引量:2
标识
DOI:10.1149/1945-7111/ad5e64
摘要
The volumetric capacity of typical Na-ion battery (NIB) negative electrodes like hard carbon is limited to less than 450 mAh cm −3 . Alloy-based negative electrodes such as phosphorus (P), tin (Sn), and lead (Pb) more than double the volumetric capacity of hard carbon, all having a theoretical volumetric capacity above 1,000 mAh cm −3 in the fully sodiated state. These alloy materials have massive volume expansion, with P expanding by almost 300% and both Sn and Pb expanding to about 400% of their initial volumes when fully sodiated. This work shows that despite this large volume change, Sn and Pb have excellent half-cell cycling performance, including high Coulombic efficiency. A blended P-hard carbon cell shows promising initial performance despite P having far lower electronic conductivity than either Sn or Pb. Overall, it is expected that these Na-alloying elements will be needed to increase the volumetric energy density of NIBs to compete with low-cost lithium iron phosphate-based cells. In fact, one company, UNIGRID, has recently demonstrated cylindrical Na-ion cells that use a pure tin negative electrode, dramatically increasing the volumetric energy density of Na-ion technology.
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