Sulfur-doped 3D hierarchical porous carbon network toward excellent potassium-ion storage performance

被引:0
作者
Dan Wang [1 ]
KangHui Tian [1 ]
Jie Wang [1 ]
ZhiYuan Wang [1 ,2 ,3 ]
ShaoHua Luo [1 ,2 ,3 ]
YanGuo Liu [1 ,2 ,3 ]
Qing Wang [1 ,2 ,3 ]
YaHui Zhang [1 ,2 ,3 ]
AiMin Hao [1 ,2 ,3 ]
TingFeng Yi [1 ,2 ,3 ]
机构
[1] School of Materials Science and Engineering, Northeastern University
[2] Key Laboratory of Dielectric, Electrolyte Functional Materia-Hebei Province
[3] School of Resources and Materials, Northeastern University
关键词
D O I
暂无
中图分类号
TM912 [蓄电池];
学科分类号
0808 ;
摘要
Carbonaceous materials are promising anode candidates for potassium-ion batteries, but currently the unsatisfactory cycling and rate performances due to the sluggish diffusion kinetic and serious structure damage during K+ insertion/extraction limit their practical application. Herein, a series of sulfur-doped porous carbons(SPCs) were prepared via a template-assisted freeze-drying followed by the carbonization and sulfuration processes at different temperatures. Among the three as-synthesized samples, SPC-600 exhibits the highest specific capacity(407 mAh·g-1 at 0.10 A·g-1), the best rate(242 mAh·g-1 at 2.00 A·g-1) and cycling performance(286 m Ah·g-1 after 800 cycles at 0.50 A·g-1). All the SPCs display higher capacities than the undoped carbon materials. The excellent electrochemical performance of SPC can be ascribed to the abundant three-dimensional porous structure together with S-doping in the disordered carbon, which is favor of providing adequate reaction active sites as well as fast ion/electron transport paths. The density functional theory(DFT) calculations further demonstrate that the sulfurdoping can promote K-ion adsorption and storage. Meanwhile, the kinetic analyses reveal that surface-induced capacitive mechanism dominates the K-ion storage process in SPCs, which contributes to ultrafast charge storage. This work provides an effective strategy for fabricating highperformance potassium-ion storage electrode materials.
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页码:2464 / 2473
页数:10
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