多硫化物
双金属片
材料科学
阴极
纳米技术
碳纳米管
催化作用
纳米颗粒
电化学
化学工程
阳极
储能
法拉第效率
吸附
碳纤维
电流密度
多孔性
电解质
纳米复合材料
电池(电)
氧化还原
合金
纳米晶
纳米尺度
电极
作者
Qian‐Cheng Zhu,Wei-Ze Sun,Lu Qiu,Hua Zhou,De-Yu Mao
标识
DOI:10.1021/acsanm.6c00065
摘要
Lithium–sulfur batteries (LSBs) have attracted significant attention as next-generation secondary batteries owing to their outstanding theoretical energy density. Nevertheless, the practical application of sulfur cathodes is hindered by intrinsic challenges, including low electronic conductivity, severe polysulfide shuttle effects, and sluggish redox kinetics, which collectively induce rapid capacity fading and poor rate capability, significantly hindering the progress of LSBs. Bimetallic catalysts have been regarded as promising electrocatalysts for lithium–sulfur batteries due to their ability to chemically interact with polysulfide and promote its kinetic conversion. Composites exhibiting synergistic effects from binary metal nanoparticles typically demonstrate superior catalytic performance compared to conventional single-metal particles. In this work, taking advantage of a bimetallic metal–organic framework (MOF), we synthesized spherical entanglement structures by intertwining iron–nickel alloy particles with carbon nanotubes (FeNi/CNT). This distinctive structural configuration offers a rich diversity of adsorption and catalytic active sites, while the porous carbon architecture further boosts its electrical conductivity. Electrochemical testing of the FeNi/CNT/S cathode showed a first discharge capacity of 963.43 mAh g–1 at a current density of 0.5C, with a remaining capacity of 464.58 mAh g–1 following 800 cycles. In brief, FeNi/CNT accelerates the polysulfide conversion and enables the high efficiency of LSBs.
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