Sodium Sulfide Cathodes Superseding Hard Carbon Pre-sodiation for the Production and Operation of Sodium-Sulfur Batteries at Room Temperature

被引:51
作者
Bloi, Luise Maria [1 ,2 ]
Pampel, Jonas [1 ,2 ]
Doerfler, Susanne [2 ]
Althues, Holger [2 ]
Kaskel, Stefan [1 ,2 ]
机构
[1] Tech Univ Dresden, Chair Inorgan Chem 1, Bergstr 66, D-01069 Dresden, Germany
[2] Fraunhofer Inst Mat & Beam Technol IWS, Winterbergstr 28, D-01277 Dresden, Germany
关键词
carbothermal reduction; hard carbon anodes; pre-sodiation; sodium-sulfur batteries; stationary energy storage; LITHIUM; PRICE;
D O I
10.1002/aenm.201903245
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study demonstrates for the first time a room temperature sodium-sulfur (RT Na-S) full cell assembled based on a pristine hard carbon (HC) anode combined with a nanostructured Na2S/C cathode. The development of cells without the demanding, time-consuming and costly pre-sodiation of the HC anode is essential for the realization of practically relevant RT Na-S prototype batteries. New approaches for Na2S/C cathode fabrication employing carbothermal reduction of Na2SO4 at varying temperatures (660 to 1060 degrees C) are presented. Initial evaluation of the resulting cathodes in a dedicated cell setup reveals 36 stable cycles and a capacity of 740 mAh g(S)(-1), which correlates to approximate to 85% of the maximum value known from literature on Na2S-based cells. The Na2S/C cathode with the highest capacity utilization is implemented into a full cell concept applying a pristine HC anode. Various full cell electrolyte compositions with fluoroethylene carbonate (FEC) additive have been combined with a special charging procedure during the first cycle supporting in situ solid electrolyte interphase (SEI) formation on the HC anode to obtain increased cycling stability and cathode utilization. The best performing cell setup has delivered a total of 350 mAh g(S)(-1), representing the first functional full cell based on a Na2S/C cathode and a pristine HC anode today.
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页数:8
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