Removal of Interstitial H<sub>2</sub>O in Hexacyanometallates for a Superior Cathode of a Sodium-Ion Battery

Jie Song(The University of Texas at Austin), Long Wang, Yuhao Lu, Jue Liu(Stony Brook University), Bingkun Guo, Penghao Xiao(The University of Texas at Austin), Jong-Jan Lee, Xiao-Qing Yang(Brookhaven National Laboratory), Graeme Henkelman, John B. Goodenough
Journal of the American Chemical Society
February 13, 2015
Cited by 943

Abstract

Sodium is globally available, which makes a sodium-ion rechargeable battery preferable to a lithium-ion battery for large-scale storage of electrical energy, provided a host cathode for Na can be found that provides the necessary capacity, voltage, and cycle life at the prescribed charge/discharge rate. Low-cost hexacyanometallates are promising cathodes because of their ease of synthesis and rigid open framework that enables fast Na(+) insertion and extraction. Here we report an intriguing effect of interstitial H2O on the structure and electrochemical properties of sodium manganese(II) hexacyanoferrates(II) with the nominal composition Na2MnFe(CN)6·zH2O (Na2-δMnHFC). The newly discovered dehydrated Na2-δMnHFC phase exhibits superior electrochemical performance compared to other reported Na-ion cathode materials; it delivers at 3.5 V a reversible capacity of 150 mAh g(-1) in a sodium half cell and 140 mAh g(-1) in a full cell with a hard-carbon anode. At a charge/discharge rate of 20 C, the half-cell capacity is 120 mAh g(-1), and at 0.7 C, the cell exhibits 75% capacity retention after 500 cycles.


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