Hierarchical Porous Carbons from Poly(methyl methacrylate)/Bacterial Cellulose Composite Monolith for High-Performance Supercapacitor Electrodes

被引:43
|
作者
Bai, Quhong [1 ]
Xiong, Qiancheng [1 ]
Li, Cong [1 ]
Shen, Yehua [1 ]
Uyama, Hiroshi [1 ,2 ]
机构
[1] Northwest Univ Xian, Coll Chem & Mat Sci, Minist Educ, Key Lab Synthet & Nat Funct Mol Chem, 1 Xuefu Ave, Xian 710127, Shaanxi, Peoples R China
[2] Osaka Univ, Grad Sch Engn, Dept Appl Chem, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2017年 / 5卷 / 10期
基金
日本学术振兴会;
关键词
Bacterial cellulose; Composite; Monolith; Poly(methyl methacrylate); Supercapacitor; INDUCED PHASE-SEPARATION; BACTERIAL CELLULOSE; FACILE FABRICATION; GRAPHENE OXIDE; NANOWIRE COMPOSITES; NANOTUBE COMPOSITE; ACTIVATED CARBON; IN-SITU; NANOCOMPOSITE; CONDUCTIVITY;
D O I
10.1021/acssuschemeng.7b02488
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study deals with hierarchical porous carbons from bacterial cellulose (BC), having a layered structure for high-performance application, such as super capacitor electrodes, fabricated from a composite monolith with unique microscopic/macroscopic morphology. A poly(methyl methacrylate) (PMMA)/BC composite monolith was first synthesized by thermally induced phase separation using ethanol and deionized water as solvents, where BC acts as the main carbon source as well as matrix and PMMA acts as the activator source producing the necessary activation material. Scanning electron microscopy analysis showed that a monolithic skeleton of PMMA was loaded uniformly on the nanofibers of BC to form a three-dimensional entangled structure of the PMMA skeleton and BC nanofibers, as observed in the microscopic view. Furthermore, the macroscopic two-dimensional layered structure of BC remained in the as-obtained composite. The specific surface area, structural features, and thermal stability were investigated by Brunauer-Emmett-Teller, X-ray diffraction, and thermogravimetric analysis studies. The resulting PMMA/BC composite was carbonized and activated by KOH at 850 degrees C. The electrochemical properties were Characterized by cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy showing that the carbonization product of the composite displayed a high specific capacitance of 266 F g(-1) at a current density of 0.50 A g(-1) and the energy density reached a maximum of 23.6 W h kg(-1) at a power density of 200 W kg(-1). Moreover, 95% of the capacitance was retained after 10,000 charge-discharge cycles, which implies exceptionally high cyclic stability. This compatible and excellent electrochemical performance of the composite, in terms of the energy density and capacitance retention, can be contributed to the characteristic porous structure of the precursor composite monolith. The present research delineates a new approach to fabricate high-performance supercapacitor materials and low-cost energy storage devices from inexpensive bioresources.
引用
收藏
页码:9390 / 9401
页数:12
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