Effect of the semi-conductive properties of the passive layer on the current provided by stainless steel microbial cathodes

被引:21
作者
Pons, Liz [1 ]
Delia, Marie-Line [1 ]
Basseguy, Regine [1 ]
Bergel, Alain [1 ]
机构
[1] Univ Toulouse, Lab Genie Chim, CNRS, F-31030 Toulouse, France
关键词
Geobacter sulfurreducens; Electroactive biofilm; Stainless steel; Mott-Schottky; Microbial fuel cell; FUEL-CELL; REDUCTIVE DECHLORINATION; CHEMICAL-COMPOSITION; ELECTRONIC-STRUCTURE; HYDROGEN-PRODUCTION; OXYGEN REDUCTION; BIOFILMS; DONORS;
D O I
10.1016/j.electacta.2010.12.039
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Geobacter sulfurreducens biofilms were formed under constant polarisation at -0.6 V vs. Ag/AgCl on stainless steel cathodes to catalyse the reduction of fumarate. The time-evolution of the current strongly depended on the quality of the inoculum. Inoculating with young cells significantly shortened the initial lag-phase and using the same inoculum improved the reproducibility of the current-time curves. The whole set of experiments showed that 254SMO stainless steel provided higher current densities (on average 14.1 A/m(2)) than biofilms formed on 316L stainless steel (on average 4.5 A/m(2)). Biofilm coverage assessed by epifluorescent microscopy showed that coverage ratios were generally higher for 316L than for 254SMO. It must be concluded that 254SMO is more efficient in transferring electrons to bacterial cells than 316L Mott-Schottky diagrams recorded on both materials under conditions of electrolysis in the absence of microorganisms showed that the surface oxide layers had similar n-type semi-conductive behaviour for potential values higher than the flat band potential. In contrast, 316L exhibited slight p-type behaviour at potential lower than the flat band potential, while 254SMO did not. The higher electrochemical performances of biocathodes formed on 254SMO are explained by semi-conductive properties of its passive layer, which prevented the p-type behaviour occurring in cathodic electrolysis conditions. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2682 / 2688
页数:7
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