硫黄
电催化剂
催化作用
氧化还原
材料科学
锂(药物)
多硫化物
离子键合
阴极
动力学
无机化学
纳米技术
化学工程
兴奋剂
化学
离子
电解质
电极
电化学
物理化学
有机化学
光电子学
内分泌学
工程类
物理
冶金
医学
量子力学
作者
Xue‐Qin Song,Da Tian,Yue Qiu,Xun Sun,Bo Jiang,Chenghao Zhao,Yu Zhang,Xianzhu Xu,Lishuang Fan,Naiqing Zhang
出处
期刊:Small
[Wiley]
日期:2021-09-14
卷期号:17 (42)
被引量:25
标识
DOI:10.1002/smll.202102962
摘要
Polysulfide shuttling and sluggish sulfur redox kinetics hinder the cyclability and rate capability of lithium-sulfur (Li-S) batteries. The intrinsic redox kinetics of sulfur cathodes strongly depends on the interaction between catalysts and sulfur species. Herein, N-doped CoTe2 is proposed as an effective dual-anchoring electrocatalyst, which can simultaneously bind Li and S atoms in lithium polysulfides via ionic Te-Li/N-Li bonding and coordinate covalent Co-S bonding. The incorporated N not only serves as enhanced lithiophilic site, but also an agent to improve the sulfiphilicity of the Co site as revealed by a series of experimental and computational results. Benefiting from these superiorities, the use of N-doped CoTe2 as a catalytic interlayer enables efficient operation of Li-S batteries in terms of impressive rate capability of 758 mAh g-1 at 4 C and very low capacity decay of 0.021% per cycle over 1000 cycles. The material and strategy demonstrated in this work may open the door toward developing more advanced Li-S electrocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI