多硫化物
氧化还原
水溶液
化学
化学工程
调解人
流量(数学)
无机化学
流动电池
氧化还原
材料科学
流动条件
电化学
作者
Qianru Chen,Yilong Zhu,Shao-Jian Zhang,Xun Zhao,Zhihao Tian,Junnan Hao,Shi-Zhang Qiao
出处
期刊:Joule
[Elsevier BV]
日期:2026-03-26
卷期号:10 (6): 102362-102362
标识
DOI:10.1016/j.joule.2026.102362
摘要
Aqueous polysulfide-based redox flow batteries (RFBs) offer a low-cost alternative to vanadium-based RFBs for grid storage. However, sluggish S 4 2− -to-S 2 2− kinetics leads to large overpotential and low energy efficiency (EE). Here, we propose bislawsone as a redox mediator that facilitates S–S bond cleavage via an "anchor-drag" effect. The battery exhibits a polarization reduction from 0.47 to 0.08 V at 10 mA cm −2 and achieves a record-high EE of 90.29% among S 4 2− /S 2 2− RFBs. At 60 mA cm −2 , the battery maintains 95.75% capacity utilization, 217 times higher than the bislawsone-free counterpart and outperforming previous solid-catalyst systems. It also exhibits high EE retention (92.43%) and capacity retention (97.88%) over 2,200 cycles. Reduced-state bislawsone alone is highly air-sensitive, and the bislawsone-only RFB with full charge fails after 2-h resting without an inert atmosphere. Conversely, spontaneous electron transfer generates air-tolerant S 2 2− in the bislawsone-polysulfide system, enabling 87.81% capacity retention after 168 h of resting.
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