journal article·2019-03-08

Efficient Trapping and Catalytic Conversion of Polysulfides by VS4 Nanosites for Li–S Batteries

Sizhe Wang, Haiyuan Chen, Jiaxuan Liao, Qian Sun, Feipeng Zhao, Jing Luo, Xiaoting Lin, Xiaobin Niu, Mengqiang Wu, Ruying Li, Xueliang Sun

ACS Energy Letters· Volume 4· Issue 3
Publisher page

Abstract

Massive efforts have been devoted to enhancing performances of Li–S batteries to meet the requirements of practical applications. However, problems remain in enhancing the energy density and improving the cycle life. We present a free-standing structure of walnut-shaped VS4 nanosites combine with carbon nanotubes (NTs) as cathodes. In this framework, NT arrays provide high surface area and conductivity for high sulfur loadings, and VS4 nanosites facilitate trapping and catalytic conversions of lithium polysulfides. The synergistic effects of free-standing NT arrays and VS4 nanosites have enabled high rate capability up to 6 C and long-term cycling with a low decay rate of 0.037% up to 1200 cycles at 2 C. Moreover, the designed cathode can achieve high areal capacities up to ∼13 mAh·cm–2 and estimated gravimetric energy density of 243.4 Wh·kg–1 at a system level, demonstrating great potential in practical applications of Li–S batteries.
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Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced Battery Technologies Research

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Affiliations

School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, People’s Republic of China

Department of Mechanical and Materials Engineering, University of Western Ontario, London, Ontario N6A 5B9, Canada

Funding

National Natural Science Foundation of China · Canada Foundation for Innovation · Natural Sciences and Engineering Research Council of Canada · China Scholarship Council · Department of Science and Technology of Sichuan Province · Canada Research Chairs · Western University · National Defense Science and technology innovation special zone project

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