多硫化物
氧化还原
双功能
催化作用
电池(电)
合理设计
硫黄
蒽醌
化学
动力学
化学工程
材料科学
电化学
锂硫电池
同种类的
无机化学
双功能催化剂
工作(物理)
纳米技术
储能
流动电池
电化学动力学
拉曼光谱
限制
能量转换效率
作者
Yi Liu,Ruixin Lv,Yuhang Zhang,Jiahao Du,Mingfang Yang,Yangyang Cao,Chong Luo
摘要
Lithium‐sulfur (Li‐S) batteries are highly promising for high‐specific‐energy batteries due to high energy density and low cost. However, the dissolved lithium polysulfide (LiPSs) together with sluggish reaction kinetics and pronounced LiPSs shuttling, bring about severely limiting battery performance. Herein, an anthraquinone (AQ)‐based homogeneous catalytic strategy is proposed to accelerate sulfur redox conversion, employing soluble 2‐bromoanthraquinone (2‐BT) as a bifunctional redox mediator. By introducing a bromo substituent, a redox mediator with well‐matched potentials for catalyzing Li 2 S oxidation and sulfur reduction was obtained, thereby promoting the solid‐liquid‐solid conversion of sulfur and suppressing the polysulfide shuttle effect and polarization. In situ Raman results further reveal that 2‐BT accelerates sulfur reduction and elevates the formation potential of polysulfides, thereby effectively promoting the solid–liquid conversion process in Li‐S batteries. Furthermore, DRT analysis demonstrates that, during charging, the introduction of 2‐BT reduces the interfacial resistance associated with the solid–liquid conversion during Li 2 S oxidation. Therefore, the Li‐S cells containing 2‐BT deliver an initial specific capacity of 832 mAh g −1 at 1 C, retaining 96.3% of capacity after 450 cycles. This work provides a rational molecular design strategy for an AQ‐based homogeneous catalyst and offers an effective approach to improving the reaction kinetics and interfacial stability of Li‐S batteries.
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