Dong Qin, Wang Tao, Gan Ruiyi, Fu Na, Li Cunpu, Wei Zidong
School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China.
ACS Appl Mater Interfaces. 2020 May 6;12(18):20596-20604. doi: 10.1021/acsami.0c04554. Epub 2020 Apr 26.
Lithium-sulfur (Li-S) batteries are promising next-generation high-density energy storage systems due to their advantages of high theoretical specific capacity, environmental compatibility, and low cost. However, high-order polysulfides dissolve in the electrolyte and subsequently lead to the undesired polysulfide shuttle effect, which hinders the commercialization of Li-S batteries. To tackle this issue, morpholine molecules were successfully grafted onto a commercial polypropylene separator. Density functional theory (DFT) calculations were performed and revealed that morpholine side chains could equally and reversibly grasp all the high-order polysulfides. This diatomic chemisorption adjusted the transformation process among the sulfur-related compounds. The modified separator battery possessed a discharge capacity as high as 827.8 mAh·g after 500 cycles at 0.5 C. The low capacity fading rate, symmetrical cyclic voltammogram, and retention of the electrode morphology all suggest that the diatomic equal adsorption approach can successfully suppress the polysulfide shuttle effect while maintaining excellent battery performance.
锂硫(Li-S)电池因其具有高理论比容量、环境兼容性好和成本低等优点,是很有前景的下一代高密度储能系统。然而,高阶多硫化物溶解在电解质中,随后导致不良的多硫化物穿梭效应,这阻碍了锂硫电池的商业化。为了解决这个问题,吗啉分子成功地接枝到商用聚丙烯隔膜上。进行了密度泛函理论(DFT)计算,结果表明吗啉侧链可以平等且可逆地捕获所有高阶多硫化物。这种双原子化学吸附调节了硫相关化合物之间的转化过程。改性隔膜电池在0.5 C下经过500次循环后,放电容量高达827.8 mAh·g。低容量衰减率、对称循环伏安图和电极形态的保持都表明,双原子均等吸附方法可以成功抑制多硫化物穿梭效应,同时保持优异的电池性能。