Melamine modified carbon felts anode with enhanced electrogenesis capacity toward microbial fuel cells

被引:33
作者
Xie, Yang'en [1 ]
Ma, Zhaokun [1 ]
Song, Huaihe [1 ]
Stoll, Zachary A. [2 ]
Xu, Pei [2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing Key Lab Elect Proc & Technol Mat, Beijing 100029, Peoples R China
[2] New Mexico State Univ, Dept Civil Engn, Las Cruces, NM 88003 USA
关键词
Microbial fuel cells; Anode materials; Carbon felts; Modification; Melamine; POWER-GENERATION; CLOTH ANODES; NANOFIBERS; PYROLYSIS; NANOTUBES;
D O I
10.1016/j.jechem.2016.11.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Surface electropositivity and low internal resistance are important factors to improve the anode performance in microbial fuel cells (MFCs). Nitrogen doping is an effective way for the modification of traditional carbon materials. In this work, heat treatment and melamine were used to modify carbon felts to enhance electrogenesis capacity of MFCs. The modified carbon felts were characterized using X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), atomic force microscopy (AFM) and malvern zeta potentiometer. Results show that the maximum power densities under heat treatment increase from 276.1 to 423.4 mW/m(2) (700 degrees C) and 461.5 mW/m(2) (1200 degrees C) and further increase to 472.5 mW/m(2) (700 degrees C) and 515.4 mW/m(2) (1200 degrees C) with the co-carbonization modification of melamine. The heat treatment reduces the material resistivity, improves the zeta potential which is beneficial to microbial adsorption and electron transfer. The addition of melamine leads to the higher content of surface pyridinic and quaternary nitrogen and higher zeta potential. It is related to higher MFCs performance. Generally, the melamine modification at high temperature increases the feasibility of carbon felt as MFCs's anode materials. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:81 / 86
页数:6
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