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A metal-organic framework-based electrocatalytic membrane boosts redox kinetics of lithium-sulfur batteries
被引:8
|作者:
Wu, Qian
[1
]
Zhao, Xinlu
[1
]
Zhou, Tianqing
[1
]
Jia, Aizhong
[1
]
Luo, Yuhong
[1
]
Li, Jingde
[1
]
Wu, Feichao
[1
]
机构:
[1] Hebei Univ Technol, Hebei Prov Key Lab Green Chem Technol & High Effic, Tianjin Key Lab Chem Proc Safety, Sch Chem Engn & Technol, Tianjin 300130, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Lithium-sulfur batteries;
Co-ZIF-9;
sheets;
Electrocatalytic membrane;
Polysulfide;
DOPED CARBON NANOFIBERS;
INTERLAYER;
POLYSULFIDES;
D O I:
10.1016/j.est.2023.108596
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
The shuttle behavior and sluggish conversion kinetics of polysulfides significantly impede the commercialization of lithium-sulfur (Li-S) batteries. Herein, we report a membrane-based electrocatalytic interlayer that consists of metal-organic framework (MOF) Co-ZIF-9 sheets and carbon nanotubes (CNT) for these issues, which is facilely weaved by vacuum filtration. The fully exposed active sites of ZIF-9 sheets endow this interlayer an efficient anchoring ability towards polysulfides, therefore efficaciously suppressing the polysulfides shuttle, and, more importantly, a strong electrocatalytic effect to accelerate the redox kinetics. Meanwhile, the threedimensional cross-linked network structured by the conductive CNT and MOF material favours a rapid ion and electron transport, and the full utilization of adsorption and catalytic sites. As a consequence, this interlayer exhibits an excellent rate performance (a capacity up to 817 mAh g-1 under 5 C), an exceptional cyclic stability (a tiny decay of 0.019% for 1000 cycles at 1 C) and a distinctive high-sulfur loading performance (7.2 mg cm-2) under a reduced electrolyte content. This study provides inspirations for the rational design of MOF-based nanostructures that can validly anchor polysulfides and catalyze their conversion for high-powered Li-S batteries.
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页数:9
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