电解质
电化学
氧化还原
有机自由基电池
阳极
阴极
解耦(概率)
储能
电极
材料科学
化学工程
容量损失
比能量
自放电
锂(药物)
化学
无机化学
热力学
医学
功率(物理)
物理
物理化学
控制工程
工程类
内分泌学
作者
Songshan Bi,Yanyu Zhang,Huimin Wang,Jin‐Lei Tian,Zhiqiang Niu
标识
DOI:10.1002/anie.202312172
摘要
Lithium||sulfur (Li||S) batteries are considered as one of the promising next-generation batteries due to the high theoretical capacity and low cost of S cathodes, as well as the low redox potential of Li metal anodes (-3.04 V vs. standard hydrogen electrode). However, the S reduction reaction from S to Li2 S leads to limited discharge voltage and capacity, largely hindering the energy density of Li||S batteries. Herein, high-energy Li||S hybrid batteries were designed via an electrolyte decoupling strategy. In cathodes, S electrodes undergo the solid-solid conversion reaction from S to Cu2 S with four-electron transfer in a Cu2+ -based aqueous electrolyte. Such an energy storage mechanism contributes to enhanced electrochemical performance of S electrodes, including high discharge potential and capacity, superior rate performance and stable cycling behavior. As a result, the assembled Li||S hybrid batteries exhibit a high discharge voltage of 3.4 V and satisfactory capacity of 2.3 Ah g-1 , contributing to incredible energy density. This work provides an opportunity for the construction of high-energy Li||S batteries.
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