青岛科技大学  English 
朱晓东
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教授 博士生导师  
硕士生导师  

教师拼音名称:zhuxiaodong

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职称:教授

毕业院校:哈尔滨工业大学

学术荣誉:

2019 当选:省高端人才

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曾获荣誉:

2019-09-26 泰山学者青年专家

2009-01-06 “国防科技创新团队”核心成员

2007-05-15 黑龙江省优秀毕业生(博士)

2007-06-30 哈尔滨工业大学优秀毕业生

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Efficient polysulfides anchoring for Li-S batteries: Combined physical adsorption and chemical conversion in V<inf>2</inf>O<inf>5</inf> hollow spheres wrapped in nitrogen-doped graphene network

关键字:Lithium compounds;Chemical stability - Decay (organic) - Doping (additives) - Graphene - Lithium batteries - Lithium sulfur batteries - Polysulfides - Spheres - Vanadium pentoxide

摘要:Lithium-sulfur (Li-S) batteries are attracting intense attention due to its high specific capacity and low cost. However, serious lithium polysulfides (LiPS) shuttle effect and the insulating property of sulfur restrict the practical application of Li-S batteries. In this work, we put forward an efficient strategy to anchor soluble LiPS through a combination of physical adsorption and chemical conversion, which is accomplished by using a heterostructure of V<inf>2</inf>O<inf>5</inf> hollow spheres wrapped in nitrogen-doped graphene network (VOHS/NG) as the sulfur host. The nitrogen-doped graphene (NG) network not only provides excellent conductivity but also traps the LiPS rapidly with high specific surface area. The initially adsorbed LiPS chemically react with V<inf>2</inf>O<inf>5</inf> hollow spheres (VOHS) to form thiosulfate intermediates. These intermediates convert the soluble "high-order" LiPS to insoluble "low-order" LiPS. Hence, the shuttle effect can be restrained efficiently. Owing to the physical and chemical synergy of the two components, the VOHS/NG heterostructure with 71 wt% sulfur can deliver superior rate performance and excellent cycling stability. A high specific capacity of 970 mAh g<sup>−1</sup> can be obtained after 100 cycles at 0.2 C. Even cycled at 2 C for 1000 times, a reversible capability of 623 mAh g<sup>−1</sup> can still be achieved with the decay rate as low as 0.017% per cycle.<br/> © 2019 Elsevier B.V.

卷号:378

期号:No

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