Research Article

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2017, 10(11): 3698–3705

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https://doi.org/10.1007/s12274-017-1581-8

High-performance Li–S battery cathode with catalyst-like carbon nanotube-MoP promoting polysulfide redox

Yingying Mi1,2, Wen Liu1 (*), Xiaolin Li1,3, Julia Zhuang4, Henghui Zhou2, and Hailiang Wang1 (*)

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1 Department of Chemistry and Energy Sciences Institute, Yale University, West Haven, CT 06516, USA
2 College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China
3 College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China
4 Department of Chemical and Environmental Engineering, Yale University, New Haven, CT 06520, USA

Keywords: lithium-sulfur battery, metal phosphide, lithium polysulfide, long cycle
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ABSTRACT Despite promising characteristics such as high specific energy and low cost, current Li–S batteries fall short in cycle life. Improving the cycling stability of S cathodes requires immobilizing the lithium polysulfide (LPS) intermediates as well as accelerating their redox kinetics. Although many materials have been explored for trapping LPS, the ability to promote LPS redox has attracted much less attention. Here, we report for the first time on transition metal phosphides as effective host materials to enhance both LPS adsorption and redox. Integrating MoP-nanoparticle-decorated carbon nanotubes with S deposited on graphene oxide, we enable Li–S battery cathodes with substantially improved cycling stability and rate capability. Capacity decay rates as low as 0.017% per cycle over 1,000 cycles can be realized. Stable and high areal capacity (>3 mAh·cm−2) can be achieved under high mass loading conditions. Comparable electrochemical performance can also be achieved with analogous material structures based on CoP, demonstrating the potential of metal phosphides for long-cycle Li–S batteries.
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High-performance Li–S battery cathode with catalyst-like carbon nanotube-MoP promoting polysulfide redox. Nano Res. 2017, 10(11): 3698–3705 https://doi.org/10.1007/s12274-017-1581-8

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