多硫化物
硫黄
材料科学
阳极
溶解
电极
过渡金属
电池(电)
金属
化学工程
无机化学
电解质
电化学
阴极
氧化还原
化学
冶金
催化作用
有机化学
物理
工程类
物理化学
功率(物理)
量子力学
作者
Xianyong Wu,Aaron Markir,Yingjie Xu,Edward Hu,Kevin T. Dai,Chong Zhang,Woochul Shin,Daniel P. Leonard,Keun-Il Kim,Xiulei Ji
标识
DOI:10.1002/aenm.201902422
摘要
Abstract Sulfur represents one of the most promising cathode materials for next‐generation batteries; however, the widely observed polysulfide dissolution/shuttling phenomenon in metal–sulfur redox chemistries has severely restricted their applications. Here it is demonstrated that when pairing the sulfur electrode with the iron metal anode, the inherent insolubility of iron sulfides renders the shuttling‐free nature of the Fe–S electrochemical reactions. Consequently, the sulfur electrode exhibits promising performance for Fe 2+ storage, where a high capacity of ≈1050 mAh g −1 , low polarization of ≈0.16 V as well as stable cycling of 150 cycles are realized. The Fe–S redox mechanism is further revealed as an intriguing stepwise conversion of S 8 ↔ FeS 2 ↔ Fe 3 S 4 ↔ FeS, where a low volume expansion of ≈32.6% and all‐solid‐state phase transitions facilitate the reaction reversibility. This study suggests an alternative direction to exploit sulfur electrodes in rechargeable transition metal–sulfur batteries.
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