Development and characterization of aqueous sodium-ion hybrid supercapacitor based on NaTi2(PO4)3//activated carbon

被引:38
|
作者
Zhang, Shuming [1 ,2 ]
Liu, Yu [1 ]
Han, Qi [1 ,2 ]
He, Shiyang [1 ]
Zhang, Na [1 ]
Yang, Jianhua [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Hybrid supercapacitor; Aqueous electrolyte; NaTi2(PO4)(3); Activated carbon; ACTIVATED CARBON; PERFORMANCE; ELECTROLYTE; COMPOSITE; ANODE; NA4MN9O18;
D O I
10.1016/j.jallcom.2017.08.256
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, for the first time, the sodium ion intercalated compound NaTi2(PO4)(3) has been designed to function as the anode in combination with activated carbon as the cathode to develop a novel aqueous sodium-ion hybrid supercapacitor based on the Na2SO4 aqueous electrolyte. Both anode and cathode have been fabricated with a thick (>1 mm) freestanding structure. The as-proposed NaTi2(PO4)(3)//activated carbon hybrid supercapacitor exhibits a typical supercapacitor-battery behavior. During the galvanostatic charging and discharging process, a linear sloping voltage range from 0 to 0.8 V corresponding to supercapacitor has been observed and an obvious voltage plateau in the range of 0.8-1.6 V could be related with the battery characterization. The hybrid supercapacitor thus brings a much high energy density over conventional supercapacitor based on activated carbon electrode. The NaTi2(PO4)(3)//activated carbon system shows a discharge capacity of 27.5 mAh g(-1) with an average working voltage of 1.15 V, corresponding to a high energy density of 31.6 Wh kg(-1) at a power density of 23 W kg(-1) based on the total weight of active electrode materials. It also exhibits excellent cycling behavior with less than 11.7% capacitance loss after 2000 cycles at current density of 200 mA g(-1). The cell delivers a relatively high power ability of 420 W kg(-1) with the energy density of 15.5 Wh kg(-1). (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:850 / 857
页数:8
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