Enhanced Chemisorption and Catalytic Effects toward Polysulfides by Modulating Hollow Nanoarchitectures for Long-Life Lithium-Sulfur Batteries

被引:66
作者
Li, Zhonglin [1 ,2 ]
Xiao, Zhubing [1 ]
Li, Pengyue [1 ]
Meng, Xueping [1 ]
Wang, Ruihu [1 ]
机构
[1] Chinese Acad Sci, State Key Lab Struct Chem, Fujian Inst Res Struct Matter, Fuzhou 350002, Fujian, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
catalytic effect; hollow materials; ionic polymers; lithium-sulfur batteries; metal-organic frameworks; MXENE NANOSHEETS; CARBON; PERFORMANCE; CAPACITY; HOST; CONVERSION; EFFICIENT; ION; NANOPARTICLES; ADSORPTION;
D O I
10.1002/smll.201906114
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hollow nanostructures with intricate interior and catalytic effects hold great promise for the construction of advanced lithium-sulfur batteries. Herein, a double-shelled hollow polyhedron with inlaid cobalt nanoparticles encapsulated by nitrogen-doped carbon (Co/NC) nanodots (Co-NC@Co9S8/NPC) is reported, which is acquired by using imidazolium-based ionic-polymer-encapsulated zeolitic imidazolate framework-67 as a core-shelled precursor. The Co/NC nanodots promote redox kinetics and chemical adsorbability toward polysulfides, while the interconnected double shells serve as a nanoscale electrochemical reaction chamber, which effectively suppresses the polysulfide shuttling and accelerates ion/electron transport. Benefiting from structural engineering and reaction kinetics modulation, the Co-NC@Co9S8/NPC-S electrode exhibits high cycling stability with a low capacity decay of 0.011% per cycle within 2000 cycles at 2 C. The electrode still shows high rate performance and cyclability over 500 cycles even in the case of high sulfur loading of 4.5 mg cm(-2) and 75 wt% sulfur content. This work provides one type of new hollow nanoarchitecture for the development of advanced Li-S batteries and other energy storage systems.
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页数:11
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