Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/48051
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dc.contributor.authorPeng, Luoen
dc.date.accessioned2012-02-27T03:44:30Zen
dc.date.available2012-02-27T03:44:30Zen
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationPeng, L. (2012). Understanding and improving the microbial fuel cell anodic electron transfer process. Doctoral thesis, Nanyang Technological University, Singapore.en
dc.identifier.urihttps://hdl.handle.net/10356/48051en
dc.description.abstractThe cell surface c-type cytochromes (c-Cyts) of Shewanella oneidensis demonstrated irreversible electrochemistry and sluggish electron transfer (ET) rate. c-Cyts could accumulate at the Shewanella-electrode interface when a more positive potential was applied to the electrode. Such accumulation may insulate the electrode from flavins, a more effective ET pathway utilized by Shewanella. This potential-dependent physiology had been observed with Ferrimonas balearica as well, which is genetically distant from S. oneidensis. This supported the representiveness of the model exoelectrogen. To promote the heterogeneous ET through S. oneidensis outer membrane c-Cyts, the electrode was modified with carbon nanotubes (CNTs). This modification transformed the rectification behavior of the OM c-Cyts and enhanced their heterogeneous rate constant. The bioelectrocatalytic current generation recorded by chronoamperometry was increased for over 80 times. Furthermore, in a fuel cell catalyzed by mixed microbial consortium, the CNT modified anode was shown to enhance power generation with promoted ET kinetics.en
dc.format.extent153 p.en
dc.language.isoenen
dc.subjectDRNTU::Engineering::Environmental engineering::Environmental protectionen
dc.titleUnderstanding and improving the microbial fuel cell anodic electron transfer processen
dc.typeThesisen
dc.contributor.supervisorWang Jing-Yuanen
dc.contributor.schoolSchool of Civil and Environmental Engineeringen
dc.description.degreeDoctor of Philosophy (CEE)en
dc.contributor.researchResidues and Resource Reclamation Centreen
dc.identifier.doi10.32657/10356/48051en
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