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Electrochemical and impedance characterization of Microbial Fuel Cells based on 2D and 3D anodic electrodes working with seawater microorganisms under continuous operation

机译:基于2D和3D阳极电极的微生物燃料电池与海水微生物连续运行的电化学和阻抗表征

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摘要

A mixed microbial population naturally presents in seawater was used as active anodic biofilm of two Microbial Fuel Cells (MFCs), employing either a 2D commercial carbon felt or 3D carbon-coated Berl saddles as anode electrodes, with the aim to compare their electrochemical behavior under continuous operation. After an initial increase of the maximum power density, the felt-based cell reduced its performance at 5months (from 7 to 4μWcm(-2)), while the saddle-based MFC exceeds 9μWcm(-2) (after 2months) and maintained such performance for all the tests. Electrochemical impedance spectroscopy was used to identify the MFCs controlling losses and indicates that the mass-transport limitations at the biofilm-electrolyte interface have the main contribution (>95%) to their internal resistance. The activation resistance was one order of magnitude lower with the Berl saddles than with carbon felt, suggesting an enhanced charge-transfer in the high surface-area 3D electrode, due to an increase in bacteria population growth.
机译:天然存在于海水中的混合微生物种群被用作两个微生物燃料电池(MFC)的活性阳极生物膜,采用2D商业碳毡或3D碳涂层的Berl鞍作为阳极电极,目的是比较它们在以下情况下的电化学行为连续运行。在最大功率密度的初始增加后,基于毡的单元格在5个月(从7减少到4μWcm(-2))降低其性能,而基于鞍型的MFC超过9μWcm(-2)(在2个月后)并保持这种状态所有测试的性能。电化学阻抗谱用于识别控制损失的MFC,并表明生物膜-电解质界面的质量迁移限制对其内阻起主要作用(> 95%)。 Berl鞍座的活化阻力比碳毡的活化电阻低一个数量级,这表明由于细菌种群的增长,高表面积3D电极的电荷转移增强了。

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