Xing Ye, Fang Wu, Zhiyu Xue, Haowei Yuan, Shijie Mei, Jiacheng Wang, Ruizhe Yang, Xiaomeng Wu, Xiaoli Zhao, Hong Pan, Qinyong Zhang, Yong Xiang, Ming Huang, Fei Li
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引用次数: 0
摘要
锂硫(Li-S)电池被认为是面向未来的储能系统的潜在候选电池。然而,锂多硫化物(LiPSs)的穿梭效应和缓慢的反应动力学阻碍了它们的实际应用。缓解这些挑战的关键策略是开发高效的异质结催化剂,以提高反应动力学并抑制穿梭效应。本研究引入了 NiS2-CoS2 异质结来应对这些挑战,并利用密度泛函理论(DFT)计算确定了 5 × 5 晶面构型的最佳组合。确定的 NiS2(210)-CoS2(200)组合为锂离子电池提供了出色的锚定效应和催化特性,显著提高了速率性能(2 C 时为 839.9 mAh g-1,3 C 时为 730.8 mAh g-1)和循环稳定性。此外,原位拉曼和 X 射线衍射 (XRD) 分析表明,NiS2-CoS2 异质结能迅速催化锂多糖的转化,减少它们向锂阳极的迁移,从而抑制穿梭效应。过渡金属硫化物异质结的设计策略为加速多硫化物转化动力学提供了一种有效的方法,从而有效地解决了锂-S 电池的局限性。
Accelerated Polysulfide Conversion by Rationally Designed NiS2-CoS2 Heterostructure in Lithium–Sulfur Batteries
Lithium–sulfur (Li–S) batteries are considered as potential candidates for future-oriented energy storage systems. However, their practical deployment is hampered by the shuttle effect and the sluggish reaction kinetics of lithium polysulfides (LiPSs). A key strategy to mitigate these challenges is to develop efficient heterojunction catalysts to enhance reaction kinetics and suppress the shuttle effect. In this study, a NiS2-CoS2 heterojunction is introduced to address these challenges with density functional theory (DFT) calculations employed to determine the optimal combination from 5 × 5 crystal plane configurations. The identified NiS2(210)-CoS2(200) combination demonstrates excellent anchoring effects and catalytic properties for LiPSs, significantly enhancing rate performance (839.9 mAh g−1 at 2 C and 730.8 mAh g−1 at 3 C) and cycling stability. Furthermore, in situ Raman and X-ray diffraction (XRD) analyses reveal that the NiS2-CoS2 heterojunction rapidly catalyzes the conversion of LiPSs, reducing their migration toward the lithium anode and thereby suppressing the shuttle effect. The design strategy for transition metal sulfide heterojunctions offers an efficient approach to accelerating polysulfide conversion kinetics, effectively addressing the limitations of Li–S batteries.
期刊介绍:
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