Surface-Driven Sodium Ion Energy Storage in Nanocellular Carbon Foams

被引:235
|
作者
Shao, Yuyan [1 ]
Xiao, Jie [1 ]
Wang, Wei [1 ]
Engelhard, Mark [1 ]
Chen, Xilin [1 ]
Nie, Zimin [1 ]
Gu, Meng [1 ]
Saraf, Laxmikant V. [1 ]
Exarhos, Gregory [1 ]
Zhang, Ji-Guang [1 ]
Liu, Jun [1 ]
机构
[1] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
Energy storage; sodium battery; surface driven reaction; oxygen functional group; nanocellular carbon foams; LONG CYCLE LIFE; LITHIUM BATTERIES; ELECTRODE MATERIALS; LOW-COST; ELECTROCHEMICAL INTERCALATION; POSITIVE ELECTRODE; FUNCTIONAL-GROUPS; CATHODE MATERIAL; ANODE MATERIAL; METAL OXIDE;
D O I
10.1021/nl401995a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sodium ion (Na+) batteries have attracted increased attention for energy storage due to the natural abundance of sodium, but their development is hindered by poor intercalation property of Na+ in electrodes. This paper reports a detailed study of high capacity, high rate sodium ion energy storage in functionalized high-surface-area nanocellular carbon foams (NCCF). The energy storage mechanism is surface-driven reactions between Na+ and oxygen-containing functional groups on the surface of NCCF. The surface reaction, rather than a Na+ bulk intercalation reaction, leads to high rate performance and cycling stability due to the enhanced reaction kinetics and the absence of electrode structure change. The NCCF makes more surface area and surface functional groups available for the Na+ reaction. It delivers 152 mAh/g capacity at the rate of 0.1 A/g and a capacity retention of 90% for over 1600 cycles.
引用
收藏
页码:3909 / 3914
页数:6
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