多硫化物
催化作用
硫黄
分离器(采油)
材料科学
拉曼光谱
化学工程
密度泛函理论
氧化还原
Atom(片上系统)
纳米技术
化学
电极
无机化学
物理化学
计算化学
有机化学
计算机科学
冶金
热力学
物理
电解质
工程类
光学
嵌入式系统
作者
Weitao Jing,Qiang Tan,Yue Duan,Kunyang Zou,Xin Dai,Yuanyuan Song,Ming Shi,Junjie Sun,Yuanzhen Chen,Yongning Liu
出处
期刊:Small
[Wiley]
日期:2022-11-24
卷期号:19 (4)
被引量:38
标识
DOI:10.1002/smll.202204880
摘要
Lithium-sulfur (Li-S) batteries have attracted considerable attention owing to their extremely high energy densities. However, the application of Li-S batteries has been limited by low sulfur utilization, poor cycle stability, and low rate capability. Accelerating the rapid transformation of polysulfides is an effective approach for addressing these obstacles. In this study, a defect-rich single-atom catalytic material (Fe-N4/DCS) is designed. The abundantly defective environment is favorable for the uniform dispersion and stable existence of single-atom Fe, which not only improves the utilization of single-atom Fe but also efficiently adsorbs polysulfides and catalyzes the rapid transformation of polysulfides. To fully exploit the catalytic activity, catalytic materials are used to modify the routine separator (Fe-N4 /DCS/PP). Density functional theory and in situ Raman spectroscopy are used to demonstrate that Fe-N4 /DCS can effectively inhibit the shuttling of polysulfides and accelerate the redox reaction. Consequently, the Li-S battery with the modified separator achieves an ultralong cycle life (a capacity decay rate of only 0.03% per cycle at a current of 2 C after 800 cycles), and an excellent rate capability (894 mAh g-1 at 3 C). Even at a high sulfur loading of 5.51 mg cm-2 at 0.2 C, the reversible areal capacity still reaches 5.4 mAh cm-2 .
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