过电位
材料科学
催化作用
多硫化物
氧化还原
储能
同种类的
流动电池
电化学
化学工程
电池(电)
分解
离子键合
流量(数学)
二硫键
无机化学
纳米技术
电化学能量转换
能量转换
键能
限制
电极
硫黄
电化学储能
组合化学
阳极
水溶液
离子
作者
Xinyu Guo,Mingjun Nan,Wanyao Sun,Xiyu Liu,Xiangkun Ma
标识
DOI:10.1021/acsami.6c00664
摘要
Sulfur-based flow batteries (SFBs) attract attention for large-scale energy storage due to the abundance and low cost of sulfur, as well as their simple design; however, they face challenges such as sluggish polysulfide redox kinetics, which cause high overpotentials and low efficiency. Herein, we introduce highly active quinone-based homogeneous molecular catalysts in the SFBs to alter the ionic arrangement around S(0) atoms, reducing the strong binding of disulfide bonds and thereby enhancing the electrochemical activity of polysulfides. The DHBQ catalyst could significantly lessen the overpotential to 280 mV (from 409 mV) at 20 mA cm –2 and increase the capacity to 10.8 Ah L –1 (over three times that of the untreated one). A polysulfide-ferrocyanide flow battery was demonstrated for 200 cycles at 40 mA cm –2 with a 100% capacity retention rate. These improvements highlight the effectiveness of quinone-based homogeneous catalysts in overcoming the bottlenecks of SFBs, offering a promising strategy for their practical application in long-duration and large-scale energy storage systems.
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