A green and scalable route to yield porous carbon sheets from biomass for supercapacitors with high capacity

被引:402
作者
Wang, Cunjing [1 ,3 ]
Wu, Dapeng [1 ,4 ]
Wang, Hongju [1 ,2 ]
Gao, Zhiyong [1 ,4 ]
Xu, Fang [1 ,2 ]
Jiang, Kai [1 ,2 ]
机构
[1] Henan Normal Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Henan Prov Green Mfg Fine, Minist Educ,Key Lab Green Chem Media & React, Xinxiang 453007, Henan, Peoples R China
[2] Henan Normal Univ, Sch Environm, Xinxiang 453007, Henan, Peoples R China
[3] Xinxiang Univ, Sch Chem & Chem Engn, Xinxiang 453003, Henan, Peoples R China
[4] Henan Normal Univ, Henan Key Lab Boron Chem & Adv Energy Mat, Xinxiang 453007, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFORMANCE ELECTRODE MATERIALS; DOUBLE-LAYER CAPACITORS; ELECTROCHEMICAL CAPACITORS; BATTERY ANODES; NITROGEN; NANOSHEETS; OXYGEN; SILK;
D O I
10.1039/c7ta07579k
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
A green and scalable route is developed to prepare hierarchical porous carbon sheets (HPCS) from biomass (cornstalk) directly under an air atmosphere instead of inert gas protection. In addition, the method adopts non-toxic NaCl and KCl mixed salt as reaction media to regulate the activation process, which avoids the corrosive and poisonous KOH and ZnCl2 reagents. Meanwhile, the porous structures of HPCS can be well-manipulated by the salt templates and the etching effects of the oxygen atom as well as the high energy molten salt media. The as-obtained HPCS consist of an ultra-thin sheet structure (similar to 4.6 nm in thickness) and abundant hierarchical pores, which facilitates electrolyte diffusion and ion transfer. In addition, the high specific surface area of 1588 m(2) g(-1) provides sufficient active sites and the rich O doping introduces pseudocapacitance. Therefore, the as-prepared HPCS exhibit a high specific capacitance of 407 F g(-1) at 1 A g(-1) in a three-electrode system. Moreover, the assembled symmetric supercapacitor in a two-electrode system also exhibits an outstanding specific capacitance of 413 F g(-1) at 0.5 A g(-1), an excellent rate capacity and a long-term cycling stability with 92.6% of initial capacitance retention after 20 000 cycles at 5 A g(-1), which are comparable to those of the porous carbons activated with traditional methods. It is expected that this green and facile technique could serve as an effective and scalable method to prepare optimized HPCS with tunable porous structures from biomass for electrochemical energy storage applications.
引用
收藏
页码:1244 / 1254
页数:11
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