WN0.67-Embedded N-doped Graphene-Nanosheet Interlayer as efficient polysulfide catalyst and absorbant for High-Performance Lithium-Sulfur batteries

多硫化物 纳米片 石墨烯 材料科学 化学工程 电化学 催化作用 电解质 分离器(采油) 成核 纳米技术 电极 化学 有机化学 物理化学 工程类 热力学 物理
作者
Fei Ma,Bo Yu,Xiaojuan Zhang,Ziheng Zhang,Katam Srinivas,Xinqiang Wang,Dawei Liu,Bin Wang,Wanli Zhang,Qi Wu,Yuanfu Chen
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:431: 133439-133439 被引量:53
标识
DOI:10.1016/j.cej.2021.133439
摘要

• A novel interlayer of WN 0.67 @NG for high-performance Li-S batteries is fabricated. • Multifunctional WN 0.67 @NG can be used as efficient polysulfide catalyst and absorbant. • Li-S cell with WN 0.67 @NG/PP delivers outstanding electrochemical performance. • Excellent performance is attributed to synergistic effect of WN 0.67 and nitrogen-doped graphene. Lithium-sulfur (Li-S) battery has attracted wide research attention due to its high energy density, high earth-abundance and low-cost. However, the dissolution of lithium polysulfides (LiPSs) and corresponding shuttle will lead to serious capacity degradation and worse cycling stability of Li-S batteries. To address such issues, herein, we firstly present a novel interlayer of WN 0.67 -embedded N-doped graphene-nanosheets (WN 0.67 @NG) via a facile solvothermal reaction followed by nitriding treatment. The Li-S cell equipped with WN 0.67 @NG modified polypropylene (PP) separator exhibits outstanding electrochemical performances: a long-term stability with only a capacity decay of 0.07% per cycle over 200 cycles and a large capacity of 725 mAh g −1 at 4C; interestingly, a favorable capacity of 776 mAh g −1 can be maintained after 100 cycles at 0.2C for assembled Li-S pouch cell under a high sulfur loading conditions of 4.3 mg cm −2 with lean electrolyte occupation (6 μL mg −1 ). The outstanding performance can be attributed to the following advantages of WN 0.67 @NG interlayer: the high conductivity of NG sheets can facilitate the electron transfer and act as a physical block for restricting the LiPSs shuttle; most importantly, the polar WN 0.67 nanoneedles embedded on the NG sheets not only provide abundant active sites for chemisorption and catalytic conversion of LiPSs, but also contribute to the nucleation and growth of Li 2 S; further theoretical calculations and in-situ Raman spectra clearly reveal the adsorption and catalytic conversion mechanism of WN 0.67 @NG interlayer at the molecular level. The work provides new insight into rational design and facile fabrication of multifunctional separators for industrial applications in high-performance Li-S batteries.

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