过电位
电解质
溶解度
动力学
化学
无机化学
电池(电)
化学工程
扩散
三氟甲磺酸
氧化还原
材料科学
降级(电信)
电化学
活化能
金属
化学动力学
储能
沉积(地质)
电化学动力学
电极
作者
Huazhao Yang,Mengting Gao,Xianxian Zhou,Donghong Duan,Ji‐Min Cao,Shibin Liu
标识
DOI:10.1016/j.jpowsour.2024.234592
摘要
The development of room-temperature sodium sulfur batteries is severely constrained by the sluggish solid-solid conversion kinetics of Na2S/Na2S2 and the accumulation of "dead Na2S/Na2S2". Here, we accelerate the conversion kinetics of Na2S/Na2S2 as well as reduce the accumulation of "dead Na2S/Na2S2" by 1-butyl-1-methylpyrrolidine trifluoromethanesulfonate ([P14][OTf]) ionic liquid additive that is compatible with metallic Na and has high Na2S/Na2S2 solubility. The results of three-electrode kinetics tests show a significant enhancement of the apparent redox kinetics of Na2S/Na2S2 through increasing its concentration. During battery cycling, the increase in Na2S/Na2S2 concentration can induce the formation of three-dimensional Na2S deposition and reduce the coverage of the electrode effective electroactive area, thus decreasing the battery polarization, especially at high rates. In addition, high Na2S/Na2S2 solubility can promote the reuse of "dead Na2S/Na2S2" and greatly improve the utilization of active material. At 2C rate, 351 mAh g−1 can be maintained after 800 cycles, and the capacity decay per cycle is 0.046 %. The rate and cycle performance of the battery are greatly improved. Further, a mechanism is proposed for the enhancement of battery performance via overpotential and diffusion theories.
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