氧化还原
阴极
材料科学
电解质
水溶液
硫黄
调解人
电池(电)
化学工程
无机化学
半反应
能量密度
储能
动能
有机自由基电池
电流密度
工作(物理)
电化学
纳米技术
充电周期
多硫化物
离子
作者
Sibo Wang,Yang Zhang,Wanlong Wu,Quanwei Jiang,Hua‐Yu Shi,Xiaoqi Sun
摘要
ABSTRACT Aqueous Zn─S batteries are promising energy storage systems with high theoretical capacity and low cost. However, the direct conversion between S and ZnS at the cathode suffers extremely sluggish reaction kinetics, which further decay rapidly upon the increase of current density and active material loading. Facing these challenges, we herein present a bi‐directional redox mediator strategy and identify a self‐adjusted Cu‐based candidate. It possesses two redox couples whose potentials are on either side of the thermodynamic redox potential of S/ZnS reaction while between its kinetic oxidation and reduction potentials. These alignments enable the bi‐directional mediator to catalyze the charge and discharge processes using either redox couple, respectively. As a result, the sulfur cathode reaches a high capacity of 1629 mAh g −1 at 0.1 A g −1 . It also maintains 880 mAh g −1 after 500 cycles at 1 A g −1 , superior to rapid decay to 148 mAh g −1 after only 28 cycles with the mediator free cathode. Furthermore, with a high sulfur loading of 7.3 mg cm −2 and lean electrolyte of 7 µL mg S −1 , the Zn─S battery achieves a high areal capacity over 10 mAh cm −2 .
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