材料科学
电催化剂
阴极
多硫化物
储能
纳米纤维
纳米颗粒
化学工程
纳米技术
碳纤维
电极
电解质
电化学
锂(药物)
纳米复合材料
多孔性
复合数
复合材料
化学
工程类
内分泌学
物理
物理化学
功率(物理)
医学
量子力学
作者
Jiayi Wang,Dan Luo,Junhua Li,Yongguang Zhang,Yan Zhao,Guofu Zhou,Lingling Shui,Zhongwei Chen,Xin Wang
出处
期刊:Nano Energy
[Elsevier]
日期:2020-12-01
卷期号:78: 105293-105293
被引量:27
标识
DOI:10.1016/j.nanoen.2020.105293
摘要
Lithium-sulfur (Li–S) batteries have been deemed as next-generation large-scale energy storage devices. However, the severe shuttle effect and sluggish conversion kinetics of lithium polysulfides significantly impede the commercialization of Li–S batteries. Herein, a unique “soft on rigid” composite consist of oxygen-deficient and Co cluster-decorated TiO2 nanofibers with carbon nanofibers (CNF), embedding numerous Co nanoparticles (denoted as “Co–TiO2-x/CNF”) is developed as a high-performance self-supporting multifunctional cathode electrocatalyst. The Co–TiO2-x/CNF offers vast surface area and enlarged porosity to homogenize sulfur distribution and enhance sulfur immobilization. The oxygen deficient Co–TiO2-x fiber and CNF establish a three-dimensional conductive framework, which accelerates electron and ion transportation within the electrode. Meanwhile, the introduction of Co clusters significantly regulate the Ti d-band center and thereby improving the Li2S6 adsorbability. Benefiting from these synergistic features, the Li2S6/Co–TiO2-x/CNF electrode delivers outstanding cycling stability (capacity fading rate of 0.03% per cycle over 500 cycles) and an improved rate capability (743 mAh g−1 at 3.0C). This design strategy based on synergy engineering could also open up new possibilities for the practical application of high performance Li–S batteries and promote the material design in related energy storage fields.
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