In situ formation of graphene layers on graphite surfaces for efficient anodes of microbial fuel cells

被引:88
作者
Tang, Jiahuan [1 ]
Chen, Shanshan [1 ]
Yuan, Yong [1 ]
Cai, Xixi [1 ]
Zhou, Shungui [1 ]
机构
[1] Guangdong Inst Ecoenvironm & Soil Sci, Guangdong Key Lab Agr Environm Pollut Integrated, Guangzhou 510650, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Microbial fuel cells; Electrochemical exfoliation; Graphene; Macroporous anodes; Graphite plate; EXTRACELLULAR ELECTRON-TRANSFER; ENERGY-STORAGE; ELECTROCHEMICAL PROPERTIES; 3-DIMENSIONAL GRAPHENE; ENHANCED PERFORMANCE; POWER OVERSHOOT; CARBON; BIOANODE; NANOCOMPOSITE; NANORIBBONS;
D O I
10.1016/j.bios.2015.04.074
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Graphene can be used to improve the performance of the anode in a microbial fuel cell (MFC) due to its good biocompatibility, high electrical conductivity and large surface area. However, the chemical production and modification of the graphene on the anode are environmentally hazardous because of the use of various harmful chemicals. This study reports a novel method based on the electrochemical exfoliation of a graphite plate (GP) for the in situ formation of graphene layers on the surface of a graphite electrode. When the resultant graphene-layer-based graphite plate electrode (GL/GP) was used as an anode in an MFC, a maximum power density of 0.67 +/- 0.034 W/m(2) was achieved. This value corresponds to 1.72-, 1.56- and 1.26-times the maximum power densities of the original GP, exfoliated-graphenemodified GP (EG/GP) and chemically-reduced-graphene-modified GP (rGO/GP) anodes, respectively. Electrochemical measurements revealed that the high performance of the GL/GP anode was attributable to its macroporous structure, improved electron transfer and high electrochemical capacitance. The results demonstrated that the proposed method is a facile and environmentally friendly synthesis technique for the fabrication of high-performance graphene-based electrodes for use in microbial energy harvesting. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:387 / 395
页数:9
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