Polydopamine as a new modification material to accelerate startup and promote anode performance in microbial fuel cells

被引:90
作者
Du, Qing [1 ]
An, Jingkun [2 ]
Li, Junhui [1 ]
Zhou, Lean [1 ]
Li, Nan [2 ]
Wang, Xin [1 ]
机构
[1] Nankai Univ, Tianjin Engn Ctr Environm Diag & Contaminat Remed, Coll Environm Sci & Engn, MOE Key Lab Pollut Proc & Environm Criteria, 38 Tongyan Rd, Tianjin 300350, Peoples R China
[2] Tianjin Univ, Sch Environm Sci & Engn, Tianjin Key Lab Indoor Air Environm Qual Control, 92 Weijin Rd, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Bioelectrochemical systems; Microbial fuel cells; Activated carbon; Polydopamine; ROLLING ACTIVATED CARBON; AIR-CATHODE; CATALYST LAYER; FE(III)-REDUCING BACTERIUM; INSPIRED IMMOBILIZATION; ENHANCED PERFORMANCE; QUATERNARY AMMONIUM; ELECTRON-TRANSFER; WASTE-WATER; REDUCTION;
D O I
10.1016/j.jpowsour.2017.01.093
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
The bacterial anode material is important to the performance of microbial fuel cells (MFCs) because its characteristics affect the biofilm formation and extracellular electron transfer. Here we find that a superhydrophilic semiconductor, polydopamine (PDA), is an effective modification material for the anode to accelerate startup and improve power density. When the activated carbon anode is added with 50% (wt.) PDA, the startup time is 14% shorter than the control (from 88 h to 76 h), with a 31% increase in maximum power density from 613 +/- 9to 803 +/- 6 mW m(-2), and the Columbic efficiency increases from 19% to 48%. These can be primarily attributed to the abundant functional groups (such as amino group, and catechol functions) introduced by PDA that improve hydrophilicity and extracellular electron transfer. PDA also increases proportions of Froteobacteria and Firmicutes families, indicating that PDA has a selective effect on anode microbial community. Our findings provide a new approach to accelerate anode biofilm formation and enhance MFC power output by modification of biocompatible PDA. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:477 / 482
页数:6
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