碳化
多硫化物
材料科学
化学工程
催化作用
纳米棒
纳米颗粒
电化学
硫黄
锂(药物)
钯
纳米复合材料
电极
纳米技术
化学
有机化学
复合材料
电解质
扫描电子显微镜
医学
物理化学
内分泌学
工程类
冶金
作者
Chongchong Zhao,Yi Yang,Yanxia Liu,Zixu Sun,Tao Zhang,Zhe Gao,Feng Huo,Yatao Zhang
标识
DOI:10.1016/j.apsusc.2023.158736
摘要
The lithium polysulfide (LiPSs) shuttle effect and sluggish conversion kinetics hinder the commercial viability of lithium-sulfur (Li-S) batteries. To improve the properties of Li-S batteries, it is imperative to establish efficient pathways for Li-ions transmission by constructing conductivity channels of high quality, and to expedite the conversion kinetics of LiPSs by employing catalysts of exceptional activity. In this study, we synthesized a spherical superstructure of metal–organic framework nanorods (SS-MOFNR) using a self-assembly strategy with zinc-metal–organic framework (Zn-MOF) nanoparticles, followed by carbonization to obtain the spherical superstructure of carbon nanorods (SS-CNR). Subsequently, palladium nanoparticles were synthesized through the reduction and uniformly dispersed onto SS-CNR. The hollow porous structure facilitates the efficient utilization of sulfur and ensures the rapid diffusion of Li-ions. Additionally, Pd nanoparticles exhibit significant catalytic activity, effectively adsorbing LiPSs and bidirectional catalytic conversion of sulfur species, thereby effectively suppressing the shuttle effect of LiPSs. Therefore S/Pd@SS-CNR electrode demonstrates commendable electrochemical efficacy, as evidenced by its initial specific capacity of 1627.7 mAh g−1 at 0.1C and maintaining a specific capacity of 766.2 mAh g−1 even after 600 cycles at 0.5C. Moreover, it exhibits favorable cycle stability at 2C, retaining a reversible capacity of 502.3 mAh g−1 after undergoing 1000 cycles.
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