硫黄
催化作用
异质结
锂(药物)
材料科学
化学工程
电池(电)
电催化剂
扩散
无机化学
阴极
氧化还原
化学
电极
物理化学
电化学
光电子学
冶金
工程类
内分泌学
生物化学
功率(物理)
物理
热力学
医学
量子力学
作者
Kaixiang Shi,Yajie Sun,Zhangshi Xiong,Junhao Li,Haoxiong Nan,Yongxian Lin,Zhigang Wei,Quanbing Liu
标识
DOI:10.1016/j.cej.2023.141794
摘要
Although rechargeable lithium-sulfur batteries (LSBs) are next generation energy storage devices, severe shuttle effect and sluggish multi-electron redox reactions compromise the practical application of LSBs. To address these issues and enable the manufacture of robust LSBs, here the use of Fe3C-Fe3P heterostructure encapsulated in nitrogen–doped carbon nanotubes ([email protected]) was synthesized. The tubular geometry of [email protected] provided buffering void to suppress volume change, and afforded conductive network to expedite the diffusion of Li+, as well as endowed plenteous active sites to absorb and catalyze the transformation of LiPSs during charge–discharge cycles. Experimental data proved that [email protected] could strengthen the “anchoring of lithium polysulfides (LiPSs)” (by Fe3P) and expedite the “diffusion of intermediate” (by CNT) as well as accelerate the “catalytic phase conversion” (by Fe3C), resulting in balanced “trapping-diffusion-conversion” dynamic process. Notably, FeCP-3 [email protected]/G/S attained an initial capacity of 1127 mAh/g with a low decay rate of 0.12 % at 1C for 300 cycles Moreover, FeCP-3 [email protected]/G/S delivered excellent battery performances under high currents of 2 and 5C for 500 cycles. This work felicitously proposed the strategy to fabricate metal carbide-phosphide heterostructure electrocatalyst for high-performance LSBs.
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