硫黄
材料科学
电化学
电池(电)
复合数
兴奋剂
锂(药物)
化学工程
锂硫电池
金属
无机化学
电极
复合材料
化学
冶金
光电子学
医学
功率(物理)
物理
物理化学
量子力学
工程类
内分泌学
作者
Huiying Wei,Qicheng Li,Bo Jin,Hui Liu
出处
期刊:Nanomaterials
[MDPI AG]
日期:2023-08-03
卷期号:13 (15): 2244-2244
被引量:7
摘要
Lithium–sulfur batteries (LSBs) have become the most promising choice in the new generation of energy storage/conversion equipment due to their high theoretical capacity of 1675 mAh g−1 and theoretical energy density of 2600 Wh kg−1. Nevertheless, the continuous shuttling of lithium polysulfides (LiPSs) restricts the commercial application of LSBs. The appearance of layered double hydroxides (LDH) plays a certain role in the anchoring of LiPSs, but its unsatisfactory electronic conductivity and poor active sites hinder its realization as a sulfur host for high-performance LSBs. In this paper, metal organic framework-derived and Ce ion-doped LDH (Ce-Ni/Fe LDH) with a hollow capsule configuration is designed rationally. The hollow structure of Ce-Ni/Fe LDH contains a sufficient amount of sulfur. Fe, Ni, and Ce metal ions effectively trap LiPSs; speed up the conversion of LiPSs; and firmly anchor LiPSs, thus effectively inhibiting the shuttle of LiPSs. The electrochemical testing results demonstrate that a lithium–sulfur battery with capsule-type S@Ce-Ni/Fe LDH delivers the initial discharge capacities of 1207 mAh g−1 at 0.1 C and 1056 mAh g−1 at 0.2 C, respectively. Even at 1 C, a lithium–sulfur battery with S@Ce-Ni/Fe LDH can also cycle 1000 times. This work provides new ideas to enhance the electrochemical properties of LSBs by constructing a hollow capsule configuration.
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