A High-Performance Polysulfide-Trapping Lithium Sulfur Battery Cathode: Cubic Co3O4 Catalyst within a Nitrogen-Doped Entangled Graphene Framework

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Narugopal Manna, Roby Soni, R. S. Young, Rhodri Jervis, Thomas S. Miller
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Abstract

The cycling performance of lithium-sulfur (Li−S) batteries is hampered by polysulfide dissolution which impacts the overall performance of Li−S batteries. Here we report the synthesis and characterization of polysulfide trapping cathode material for Li−S batteries based on Co3O4 nanocubes supported within a nitrogen-doped entangled graphene (Co3O4/NEGF). The highly porous conductive graphene network is shown to facilitate fast electron transport and ion diffusion while the nitrogen dopants and polar Co3O4 offer both abundant active sites for polysulfide conversion while promoting intermediate polysulfide binding. The porous structure allows for high sulfur loading of 76.4 wt % (S@Co3O4/NEGF), while efficiently accommodating volumetric expansion during charge-discharge. The Co3O4/NEGF cathode composite exhibited a high specific capacity of 1143 mAh g−1 at a current density of C/20 and maintained a 79 % reversible capacity after 200 cycles at C/5.

Abstract Image

高性能多硫化物捕获锂硫电池阴极:氮掺杂纠缠石墨烯框架内的立方Co3O4催化剂
锂硫(Li−S)电池的循环性能受到多硫化物溶解的影响,从而影响锂硫电池的整体性能。在这里,我们报告了基于掺杂氮的纠缠石墨烯(Co3O4/NEGF)内的Co3O4纳米立方体的锂离子电池多硫化物捕获正极材料的合成和表征。高多孔导电石墨烯网络促进了快速电子传递和离子扩散,而氮掺杂剂和极性Co3O4既为多硫化物转化提供了丰富的活性位点,又促进了中间多硫化物的结合。多孔结构允许高硫负载76.4 wt % (S@Co3O4/NEGF),同时有效地适应充放电过程中的体积膨胀。Co3O4/NEGF阴极复合材料在C/20电流密度下具有1143 mAh g−1的高比容量,在C/5电流密度下循环200次后仍保持79%的可逆容量。
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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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