首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Effective Trapping of Polysulfides Using Functionalized Thin-Walled Porous Carbon Nanotubes as Sulfur Hosts for Lithium-Sulfur Batteries
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Effective Trapping of Polysulfides Using Functionalized Thin-Walled Porous Carbon Nanotubes as Sulfur Hosts for Lithium-Sulfur Batteries

机译:用官能化薄壁多孔碳纳米管作为锂 - 硫电池硫宿主的有效诱捕多硫化物

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摘要

Owing to their high aspect ratios and structures of high-mechanical-strength conductive scaffolds, carbon nanotubes (CNTs) are considered to be one of the most promising hosts for sulfur in lithium-sulfur batteries (LSBs). However, traditional CNTs with impermeable walls are not conducive to the penetration of sulfur, resulting in a large number of sulfur exposures to the electrolyte. Therefore, it is difficult to effectively limit the shuttle effect of polysulfides. Here, a kind of thin-walled porous amorphous carbon nanotube (HCNT) is adopted as the host for sulfur in LSBs. To further alleviate the shuttle effect, oxygen-containing functional groups (OCFGs) are introduced to modify HCNTs to form HOCNTs. The S/HOCNT composite with the embedded structure is successfully constructed. The S/HOCNT cathode demonstrates glorious cycling and rate performance (798.5 mAh g(-1) at 0.2 C after 100 cycles and 511.6 mAh g(-1) at 1 C after 500 cycles). The excellent electrochemical performance of S/HOCNT can be attributed to the embedded structure of sulfur in HOCNTs, which avoids direct contact with the electrolytes and strong bonding action of OCFGs and polysulfides, effectively limiting the shuttle effect of polysulfides.
机译:由于它们的高纵横比和高机械强度导电支架的结构,碳纳米管(CNT)被认为是锂 - 硫电池(LSB)中最有前途的硫磺宿主之一。然而,具有不可渗透壁的传统CNT不利于硫的渗透,导致电解质大量硫曝光。因此,难以有效地限制多硫化物的梭效果。这里,采用一种薄壁多孔无定形碳纳米管(HCNT)作为LSB中硫的宿主。为了进一步缓解梭效果,引入含氧的官能团(OCFG)以改变HCNT以形成HOCNT。成功构建了具有嵌入式结构的S / HOCNT复合材料。 S / HOCNT阴极在500次循环后,在100次循环后,在0.2℃下,在0.2℃下,在0.2℃下显示出辉煌的循环和速率性能(798.5mAhg(-1))。 S / HOCNT的优异电化学性能可归因于霍茂的含硫的嵌入式结构,其避免了与电解质和OCFG和多硫化物的强键合作用直接接触,有效地限制了多硫化物的梭效果。

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