4.8 Article

Cobalt ferrite microspheres as a biocompatible anode for higher power generation in microbial fuel cells

Journal

JOURNAL OF POWER SOURCES
Volume 483, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2020.229170

Keywords

Cobalt ferrite; Extracellular electron transfer; Escherichia coli; Microbial fuel cell; Power density

Funding

  1. Main Research Program of the Korea Food Research Institute (KFRI) - Ministry of Science and ICT [E0187303-03]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2018R1A2B2006094]
  3. National Research Foundation of Korea [2018R1A2B2006094] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this study, spinel cobalt ferrite hierarchical flower-like microspheres were successfully fabricated and utilized as a biocompatible anode in microbial fuel cells, achieving high power output. The unique morphology and charge properties of CoFe2O4-MS promoted efficient interfacial interactions with Escherichia coli, resulting in more effective electron transfer and power generation.
In the present study, spinel cobalt ferrite hierarchical flower-like microspheres (CoFe2O4-MS) are fabricated using a hydrothermal method and utilized as a biocompatible anode in microbial fuel cells (MFCs) for power generation. A maximum power density of 1964 mW m(-2) is achieved with CoFe2O4-MS in a mediator-less MFC using Escherichia coli as a biocatalyst and glucose as a fuel. The unprecedented power generation by CoFe2O4-MS can be attributed to (i) the morphology of the flower-like CoFe2O4-MS, with a rough surface and large surface area suitable for biofilm formation, (ii) the rapid immobilization of negatively charged E. coli cells on the positively charged CoFe2O4-MS, facilitating stronger bacterial adhesion between the bacterial cells and CoFe2O4-MS, which leads to lower contact resistance and advantageous interfacial properties with rapid electron transfer, and, more importantly, (iii) enhanced interfacial charge transfer due to the presence of multi-valent cations and multiple valence states in the highly electrocapacitive CoFe2O4-MS. Thus, the enrichment of electroactive E. coli on CoFe2O4-MS produces a large number of electron-shuttling endogenous redox mediators, which promotes efficient extracellular electron transfer between E. coli and the electrocapacitive CoFe2O4-MS during the oxidation of the substrate, thus generating higher power output.

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