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In Situ Self-Formed Nanosheet MoS3/Reduced Graphene Oxide Material Showing Superior Performance as a Lithium-Ion Battery Cathode

机译:原位自成的纳米片MOS3 /氧化石墨烯氧化物材料,显示出优异的性能作为锂离子电池阴极

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摘要

Although lithium-sulfur (Li-S) batteries have 5-10 times higher theoretical capacity (1675 mAh g(-1)) than present commercial lithium-ion batteries, Li-S batteries show a rapid and continuous capacity fading due to the polysulfide dissolution in common electrolytes. Here, we propose the use of a sulfur-based cathode material, amorphous MoS3 and reduced graphene oxide (r-GO) composite, which can be substituted for the pure sulfur-based cathodes. In order to enhance kinetics and stability of the electrodes, we intentionally pulverize the microsized MoS3 sheet into nanosheets and form an ultrathin nano-SEI on the surface using in situ electrochemical methods. Then, the pulverized nanosheets are securely anchored by the oxygen functional group of r-GO. As a result, the electrochemically treated MoS3/r-GO electrode shows superior performance that surpasses pure sulfur-based electrodes; it exhibits a capacity of about 900 mAh g(-1) at a rate of 5C for 2500 cycles without capacity fading. Moreover, a full-cell battery employing the MoS3/r-GO cathode with a silicon-carbon composite anode displays a 3-5 times higher energy density (1725 Wh kg(-1)/7100 Wh L-1) than present LIBs.
机译:虽然锂 - 硫(LI-S)电池具有5-10倍的理论容量(1675mAhg(-1)),但由于目前的商用锂离子电池,Li-S电池由于多硫化物而呈现出快速和连续的容量褪色普通电解质中的溶解。这里,我们提出了使用硫基阴极材料,无定形MOS3和还原的石墨烯(R-GO)复合材料,其可以代替纯硫基阴极。为了提高电极的动力学和稳定性,我们用原位电化学方法将微化MOS3片材粉碎至纳米晶片并在表面上形成超薄纳米SEI。然后,粉碎的纳米片被R-Go的氧官能团牢固锚固。结果,电化学处理的MOS3 / R-GO电极显示出优异的性能,其超越纯硫基电极;它以5℃的速率显示出约900mAhg(-1)的容量,2500个循环,无容量衰落。此外,采用MOS3 / R-GO阴极的全电池电池,其具有硅 - 碳复合阳极的能量密度高出3-5倍(1725WHKG(-1)/ 7100WH L-1)。

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