This website uses cookies to give you the best user experience. If you continue
without changing your settings we'll assume you are happy to receive all RSC cookies.
You can change your cookie settings by navigating to our Privacy and Cookies page and following the instructions. These instructions
are also obtainable from the privacy link at the bottom of any RSC page.
Department of Physics and Astronomy, University of Southern California, 920 Bloom Walk, Seaver Science Center 215C, Los Angeles, USA
E-mail: mnaggar@usc.edu
; Fax: +1 213 740-6653
; Tel: +1 213 740-2394
Phys. Chem. Chem. Phys., 2012,14, 13802-13808
DOI:
10.1039/C2CP41185G
Received
12 Apr 2012,
Accepted
18 Jun 2012
First published online
18 Jun 2012
Dissimilatory metal-reducing bacteria are microorganisms that gain energy by transferring respiratory electrons to extracellular solid-phase electron acceptors. In addition to its importance for physiology and natural environmental processes, this form of metabolism is being investigated for energy conversion and fuel production in bioelectrochemical systems, where microbes are used as biocatalysts at electrodes. One proposed strategy to accomplish this extracellular charge transfer involves forming a conductive pathway to electrodes by incorporating redox components on outer cell membranes and along extracellular appendages known as microbial nanowires within biofilms. To describe extracellular charge transfer in microbial redox chains, we employed a model based on incoherent hopping between sites in the chain and an interfacial treatment of electrochemical interactions with the surrounding electrodes. Based on this model, we calculated the current–voltage (I–V) characteristics and found the results to be in good agreement with I–V measurements across and along individual microbial nanowires produced by the bacterium Shewanella oneidensis MR-1. Based on our analysis, we propose that multistep hopping in redox chains constitutes a viable strategy for extracellular charge transfer in microbial biofilms.
Fetching data from CrossRef. This may take some time to load.
Physical Chemistry Chemical Physics
- Information Point