阳极
电池(电)
材料科学
阴极
水溶液
电化学
电极
化学工程
电解质
化学
有机化学
量子力学
物理
工程类
物理化学
功率(物理)
作者
Qianru Chen,Junnan Hao,Shaojian Zhang,Zhihao Tian,Kenneth Davey,Shi Zhang Qiao
标识
DOI:10.1002/adma.202309038
摘要
Abstract Despite being extensively explored as cathodes in batteries, sulfur (S) can function as a low‐potential anode by changing charge carriers in electrolytes. Here, a highly reversible S anode that fully converts from S 8 0 to S 2− in static aqueous S–I 2 batteries by using Na + as the charge carrier is reported. This S anode exhibits a low potential of −0.5 V (vs standard hydrogen electrode) and a near‐to‐theoretical capacity of 1404 mA h g −1 . Importantly, it shows significant advantages over the widely used Zn anode in aqueous media by obviating dendrite formation and H 2 evolution. To suppress “shuttle effects” faced by both S and I 2 electrodes, a scalable sulfonated polysulfone (SPSF) membrane is proposed, which is superior to commercial Nafion in cost (US$1.82 m −2 vs $3500 m −2 ) and environmental benignity. Because of its ultra‐high selectivity in blocking polysulfides/iodides, the battery with SPSF displays excellent cycling stability. Even under 100% depth of discharge, the battery demonstrates high capacity retention of 87.6% over 500 cycles, outperforming Zn–I 2 batteries with 3.1% capacity under the same conditions. These findings broaden anode options beyond metals for high‐energy, low‐cost, and fast‐chargeable batteries.
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