Supercapacitors based on carbons with tuned porosity derived from paper pulp mill sludge biowaste

被引:151
作者
Wang, Huanlei [1 ,2 ]
Li, Zhi [1 ,2 ]
Tak, Jin Kwon [3 ]
Holt, Chris M. B. [1 ,2 ]
Tan, Xuehai [1 ,2 ]
Xu, Zhanwei [1 ,2 ]
Amirkhiz, Babak Shalchi [1 ,2 ]
Hayfield, Don [3 ]
Anyia, Anthony [3 ]
Stephenson, Tyler [1 ,2 ]
Mitlin, David [1 ,2 ]
机构
[1] Univ Alberta, Edmonton, AB T6G 2V4, Canada
[2] Natl Res Council Canada, Natl Inst Nanotechnol NINT, Edmonton, AB T6G 2M9, Canada
[3] Alberta Innovates Technol Futures, Bioresource Technol, Vegreville, AB T9C 1T4, Canada
关键词
DOUBLE-LAYER CAPACITORS; IONIC LIQUID ELECTROLYTE; HIGH-PERFORMANCE; ELECTROCHEMICAL CAPACITORS; ACTIVATED CARBONS; PORE-SIZE; NANOTUBES; GRAPHENE; DENSITY; STORAGE;
D O I
10.1016/j.carbon.2013.01.079
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
Hydrothermal carbonization followed by chemical activation is utilized to convert paper pulp mill sludge biowaste into high surface area (up to 2980 m(2) g(-1)) carbons. This synthesis process employs an otherwise unusable byproduct of paper manufacturing that is generated in thousands of tons per year. The textural properties of the carbons are tunable by the activation process, yielding controlled levels of micro and mesoporosity. The electrochemical results for the optimized carbon are very promising. An organic electrolyte yields a maximum capacitance of 166 F g(-1), and a Ragone curve with 30 W h kg(-1) at 57 W kg(-1) and 20 W h kg(-1) at 5450 W kg(-1). Two ionic liquid electrolytes result in maximum capacitances of 180-190 F g(-1) with up to 62% retention between 2 and 200 mV s(-1). The ionic liquids yielded energy density-power density combinations of 51 W h kg(-1) at 375 W kg(-1) and 26-31 W h kg(-1) at 6760-7000 W kg(-1). After 5000 plus charge-discharge cycles the capacitance retention is as high at 91%. The scan rate dependence of the surface area normalized capacitance highlights the rich interplay of the electrolyte ions with pores of various sizes. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:317 / 328
页数:12
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