微生物燃料电池
铁质
阳极
脱硫弧菌
硫酸盐还原菌
普通脱硫弧菌
化学
无机化学
线性扫描伏安法
硫化物
循环伏安法
计时安培法
硫酸盐
化学工程
地杆菌
电极
电化学
细菌
有机化学
生物膜
遗传学
工程类
生物
物理化学
作者
Muralidharan Murugan,Waheed Miran,Takuya Masuda,Dae S. Lee,Akihiro Okamoto
标识
DOI:10.1002/celc.201801086
摘要
Abstract The anodic oxidation of sulfide metabolically generated from sulfate is considered to be the primary mechanism of sulfate reducing bacteria (SRB) to contribute to the current generation in Microbial Fuel Cells (MFCs). However, the other redox active metabolic by‐product of conductive iron sulfide (FeS) has been seldomly studied in the context of anodic current generation. Here, we demonstrate that the biomineralized FeS increased the anodic current production in Desulfovibrio vulgaris Hildenborough, compared with that mediated by diffusive sulfate. Chronoamperometry on indium tin‐doped oxide electrodes (ITO) poised at +0.4 V (vs SHE) in the presence of lactate and sulfate showed that the presence of ferrous ion caused twice more anodic current than that in the absence of the iron. Linear Sweep Voltammetry (LSV), Scanning Electron Microscopy (SEM) and X‐ray Photoelectron Spectroscopy confirmed that the aggregation formation of cells with FeS and FeS 2 particles on the surface of the ITO electrode. These iron sulfur precipitates were more oxidized on the anode surfaces once lactate was depleted as electron source. The presented data suggests that biosynthesized FeS mediates the electron transport from D. vulgaris Hildenborough to the electrode surface. Given microbial capability of FeS biosynthesis is general among SRB, the FeS‐mediated mechanism may dominate anodic current generation of SRB in MFCs.
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