多硫化物
材料科学
分离器(采油)
有机自由基电池
催化作用
吸附
氧化还原
储能
硫黄
化学工程
无机化学
兴奋剂
电池(电)
过渡金属
纳米技术
电解质
电极
化学
有机化学
物理化学
冶金
功率(物理)
量子力学
光电子学
热力学
工程类
物理
作者
Jianbin Liu,Zhensong Qiao,Qingshui Xie,Dong‐Liang Peng,Rong‐Jun Xie
标识
DOI:10.1021/acsami.1c00494
摘要
Lithium–sulfur (Li–S) batteries are regarded as one of the most promising next-generation battery technologies owing to their ultrahigh energy density up to 2600 W h kg–1 and low cost. However, major challenges still remain in the application of Li–S batteries, such as shuttle effect and sluggish redox kinetics. Herein, it is demonstrated that phosphorus doping can not only significantly improve the polysulfide adsorption but also enhance the catalysis effects of metal–organic framework-derived CoS2 nanoboxes in Li–S batteries. Consequently, a modified separator integrated with P–CoS2 and carbon nanotubes effectively suppresses the polysulfide shuttle and propels the redox kinetics of polysulfides, thus promising higher specific discharge capacity, better rate, and stable cycle performance. Even under the high sulfur loading condition (4.8 mg cm–2), the areal discharge capacity of the cell with the functional separator can still remain at 4.5 mA h cm–2 after 100 cycles at 0.2 C. More importantly, this work may encourage more effort on anion doping for engineering the polar surface of transition-metal compounds to further mediate the interfacial redox chemistry between transition-metal compounds and polysulfides in Li–S batteries.
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