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Iron phthalocyanine and MnOx composite catalysts for microbial fuel cell applications

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journal contribution
posted on 2021-02-08, 09:59 authored by Richard Burkitt, TR Whiffen, Eileen Yu
A low cost iron phthalocyanine (FePc)-MnOx composite catalyst was prepared for the oxygen reduction reaction (ORR) in the cathode of microbial fuel cells (MFCs).The catalysts were characterised using rotating ring disc electrode technique. The n number of electrons transferred, and H2O2 production from ORR was investigated. The FePc-MnOx composite catalyst showed higher ORR reduction current than FePc and Pt in low overpotential region. MFC with composite catalysts on the cathode was tested and compared to Pt and FePc cathodes. The cell performance was evaluated in buffered primary clarifier influent from wastewater treatment plant. The membrane-less single chamber MFC generated more power with composite FePcMnOx/MON air cathodes (143mWm-2) than commercial platinum catalyst (140mWm-2) and unmodified FePc/MON (90mWm-2), which is consistent with the RRDE study.The improvement was due to two mechanisms which abate H2O2 release from the composite. H2O2 is the reactant in two processes: (i) chemical regeneration of MnOx after electro-reduction to Mn2+, and (ii) peroxide undergoing chemical disproportionation to O2 and H2O on an electrochemically aged manganese surface retained in the film. Process (i) has the potential to sustain electrochemical reduction of MnOx at cathode potentials as high as 1.0VRHE.

Funding

The Supergen Biological Fuel Cells Consortium 2010-2014 (CORE)

Engineering and Physical Sciences Research Council

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History

School

  • Aeronautical, Automotive, Chemical and Materials Engineering

Department

  • Chemical Engineering

Published in

Applied Catalysis B: Environmental

Volume

181

Pages

279 - 288

Publisher

Elsevier

Version

  • VoR (Version of Record)

Rights holder

© The Authors

Publisher statement

This is an Open Access Article. It is published by Elsevier under the Creative Commons Attribution 4.0 International Licence (CC BY 4.0). Full details of this licence are available at: https://creativecommons.org/licenses/by/4.0/

Acceptance date

2015-07-07

Publication date

2015-07-17

Copyright date

2015

ISSN

0926-3373

eISSN

1873-3883

Language

  • en

Depositor

Deposit date: 8 February 2021

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