Pseudocapacitance contribution in boron-doped graphite sheets for anion storage enables high-performance sodium-ion capacitors

被引:125
|
作者
Yu, Feng [2 ]
Liu, Zaichun [3 ,4 ]
Zhou, Renwu [2 ]
Tan, Deming [1 ]
Wang, Hongxia [2 ]
Wang, Faxing [1 ]
机构
[1] Tech Univ Dresden, Dept Chem & Food Chem, D-01062 Dresden, Germany
[2] Queensland Univ Technol, Sci & Engn Fac, Sch Chem Phys & Mech Engn, Brisbane, Qld 4001, Australia
[3] Nanjing Tech Univ, Sch Energy Sci & Engn, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Tech Univ, Inst Adv Mat, Nanjing, Jiangsu, Peoples R China
关键词
HOLLOW CARBON SPHERES; ENERGY-STORAGE; ELECTRODE MATERIALS; INTERCALATION; NANOSHEETS; ULTRAFAST; GRAPHENE; CATHODE; DENSITY; ANODE;
D O I
10.1039/c8mh00156a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Research on metal-ion hybrid capacitors is emerging as one of the hottest topics in energy storage fields because of their combination of high power and energy densities. To improve the sluggish faradaic reaction in traditional electrode materials for metal-ion hybrid capacitors, intercalation pseudocapacitive materials have been developed as attractive candidates. However, all the previously reported pseudocapacitances in intercalation/deintercalation reactions are based on cations (Li+, Na+, Zn(2+)etc.). In this work, we demonstrated the high pseudocapacitance contribution in boron-doped graphite (BG) sheets by taking advantage of anion storage. The BG electrode can reversibly store anions (PF6-) through both a surface-controlled pseudocapacitive reaction and a diffusion-limited intercalation/deintercalation reaction. The fabricated Na-ion hybrid capacitor with a BG cathode exhibits superior electrochemical performance. Density functional theory (DFT) calculation reveals that B-doping can significantly reduce the PF6- diffusion energy barrier in the graphite layers.
引用
收藏
页码:529 / 535
页数:7
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