期刊
ENERGY & ENVIRONMENTAL SCIENCE
卷 8, 期 4, 页码 1309-1316出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ee03759f
关键词
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资金
- State Key Project of Fundamental Research for Nanoscience and Nanotechnology [2011CB935900]
- National Science Foundation of China (NSFC) [21322101, 21231005]
- Ministry of Education [B12015, 113016A, ACET-13-0296]
It is desirable to develop electrode materials for advanced rechargeable batteries with low cost, long life, and high-rate capability. Pyrite FeS2, as an easily obtained natural mineral, has been already commercialized in primary lithium batteries, but encountered problems in rechargeable batteries with carbonate-based electrolytes due to the limited cycle life caused by the conversion-type reaction (FeS2 + 4M -> Fe + 2M(2)S (M = Li or Na)). Herein, we demonstrate that FeS2 microspheres can be applied in room-temperature rechargeable sodium batteries with only the intercalation reaction by simultaneously selecting a compatible NaSO3CF3/diglyme electrolyte and tuning the cut-off voltage to 0.8 V. A surprisingly high-rate capability (170 mA h g(-1) at 20 A g(-1)) and unprecedented long-term cyclability (similar to 90% capacity retention for 20 000 cycles) has been obtained. We suggest that a stable electrically conductive layer-structured NaxFeS2 was formed during cycling, which enables the highly reversible sodium intercalation and deintercalation. Moreover, 18650-type sodium batteries were constructed exhibiting a high capacity of similar to 4200 mA h (corresponding to 126 W h kg(-1) and 382 W h L-1) and a capacity retention of 97% after an initial 200 cycles at 4 A during charge-discharge. This shows that the production of rechargeable sodium batteries with FeS2 microspheres is viable for commercial utilization.
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