Kinetic Enhancement of Sulfur Cathodes by N-Doped Porous Graphitic Carbon with Bound VN Nanocrystals

被引:111
|
作者
Yang, Xinyue [1 ]
Chen, Shang [1 ]
Gong, Wenbin [2 ]
Meng, Xiaodong [1 ]
Ma, Junpeng [1 ]
Zhang, Jie [1 ]
Zheng, Lirong [3 ]
Abruna, Hector D. [4 ]
Geng, Jianxin [1 ,5 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, 15 North Third Ring East Rd, Beijing 100029, Peoples R China
[2] Xuzhou Univ Technol, Sch Phys & Energy, Xuzhou 221018, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[4] Cornell Univ, Dept Chem & Chem Biol, Baker Lab, Ithaca, NY 14853 USA
[5] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, 15 North Third Ring East Rd, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysis; lithium− sulfur batteries; metal nitride; one‐ pot synthesis; porous graphitic carbon; LITHIUM; PERFORMANCE; REDOX; POLYSULFIDES; CONVERSION; NANOSHEETS; NITROGEN; MATRIX;
D O I
10.1002/smll.202004950
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reaction kinetics of sulfur cathodes generally control the performance of lithium-sulfur (Li-S) batteries. Here, N-doped porous graphitic carbon with bound VN nanocrystals (3D VN@N-PGC), which is synthesized in one pot by heating a mixture of glucose as C source, urea as N source, and NH4VO3 as V source, is reported to be an superior electrocatalytic cathode host for Li-S batteries. Notably, the VN nanocrystals, strongly bound to the N-PGC network, form via in situ reactions among the thermolytic products of starting materials. The dopant N atoms and bound VN nanocrystals exhibit synergistic electrocatalytic effects to promote the cathode reactions of the Li-S cells. The observed enhancements are supported by density functional theory simulations and by the observation of electrocatalytic N- and V-intermediate species, via X-ray absorption near-edge structure spectroscopy. Li-S cells assembled using 3D VN@N-PGC as cathode host exhibit superior performance in terms of specific capacity (1442 mA h g(-1) at 0.1 C), rate capability (641 mA h g(-1) at 4 C), and cycle life (466 mA h g(-1) after 1700 cycles at 2 C, corresponding to a capacity decay of 0.020% per cycle). The one-pot methodology is facile and scalable and offers a new approach for synthesis of various metal nitride-containing materials for other electrocatalytic applications.
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页数:10
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