4.7 Article

Conjugated Polyelectrolyte/Bacteria Living Composites in Carbon Paper for Biocurrent Generation

期刊

MACROMOLECULAR RAPID COMMUNICATIONS
卷 43, 期 16, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202100840

关键词

biocomposites; biocurrent generation; conjugated polyelectrolytes; living materials; Shewanella oneidensis MR-1

资金

  1. National University of Singapore [R143-000-A97-133]
  2. National University of Singapore (NUS)
  3. Nanyang Technological University (NTU)
  4. National Research Foundation
  5. Ministry of Education

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In this study, a biocomposite comprising the water-soluble conjugated polyelectrolyte CPE-K and electrogenic Shewanella oneidensis MR-1 was shown to self-assemble on carbon paper electrodes, resulting in increased biocurrent extraction. The biocomposite on carbon paper outperformed its gold-coated counterparts in terms of biocurrent extraction.
Successful practical implementation of bioelectrochemical systems (BES) requires developing affordable electrode structures that promote efficient electrical communication with microbes. Recent efforts have centered on immobilizing bacteria with organic semiconducting polymers on electrodes via electrochemical methods. This approach creates a fixed biocomposite that takes advantage of the increased electrode's electroactive surface area (EASA). Here, it is demonstrated that a biocomposite comprising the water-soluble conjugated polyelectrolyte CPE-K and electrogenic Shewanella oneidensis MR-1 can self-assemble with carbon paper electrodes, thereby increasing its biocurrent extraction by approximate to 6-fold over control biofilms. A approximate to 1.5-fold increment in biocurrent extraction is obtained for the biocomposite on carbon paper relative to the biocurrent extracted from gold-coated counterparts. Electrochemical characterization revealed that the biocomposite stabilized with the carbon paper more quickly than atop flat gold electrodes. Cross-sectional images show that the biocomposite infiltrates inhomogeneously into the porous carbon structure. Despite an incomplete penetration, the biocomposite can take advantage of the large EASA of the electrode via long-range electron transport. These results show that previous success on gold electrode platforms can be improved when using more commercially viable and easily manipulated electrode materials.

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