Synergetic Interlayer in Li-S Batteries: Polysulfide-Impeding Effect of Conductive Carbon Cloth Supporting Topological-Phase Bi2Se3

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Heng Wang, Huichao Dong, Ting Kan, Hewei Luo, Ji Yan, Hirofumi Yoshikawa
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引用次数: 0

Abstract

The shuttle effect and sluggish sulfur conversion kinetics hamper the development of lithium–sulfur batteries. In this study, Bi2Se3 nanosheets were grown in-situ directly on a carbon cloth and adopted as an interlayer in lithium–sulfur batteries to accelerate sulfur chemistry kinetics. The topological phase of Bi2Se3 can effectively anchor soluble sulfur species, whereas the conductive carbon cloth provides electron transport pathways for the adsorbed polysulfides. Such a synergetic effect between the topological phase and conductive network impedes the severe shuttle effect of lithium polysulfides and accelerates the sulfur electrochemical redox reaction. Benefiting from such merits, a significantly improved specific capacity of 505 mAh g−1 at 4 C and cycling stability beyond 100 cycles with an average capacity decay rate of 0.16 % per cycle at 0.2 C was achieved when the interlayer was adopted in lithium–sulfur batteries. This study demonstrates the potential implementation of topological materials in advanced lithium–sulfur batteries.

Abstract Image

Li-S电池中的协同中间层:导电碳布支持拓扑相Bi2Se3的多硫化物阻碍效应
穿梭效应和硫转化动力学缓慢阻碍了锂硫电池的发展。在本研究中,Bi2Se3纳米片直接生长在碳布上,并作为锂硫电池的中间层来加速硫化学动力学。Bi2Se3的拓扑相可以有效地锚定可溶性硫,而导电碳布则为吸附的多硫化物提供了电子传递途径。这种拓扑相与导电网络之间的协同作用,阻碍了多硫化物锂剧烈的穿梭效应,加速了硫的电化学氧化还原反应。利用这些优点,锂硫电池在4℃时的比容量显著提高到505 mAh g−1,在0.2℃时的循环稳定性超过100次,平均每循环容量衰减率为0.16%。这项研究展示了拓扑材料在先进锂硫电池中的潜在应用。
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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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