Iron-chelated electrocatalysts for the oxygen reduction reaction (ORR) in a microbial fuel cell (MFC) were prepared from sodium ferric ethylenediamine-N,N0-bis(2- hydroxyphenylacetic acid) (FeE), sodium ferric diethylene triamine pentaacetic acid (FeD) supported on carbon Vulcan XC-72R carbon black and multi-walled carbon nanotubes (CNTs). Catalyst morphology was investigated by TEM; and the total surfaces areas as well as the pore volumes of catalysts were examined by nitrogen physisorption characterization. The catalytic activity of the iron based catalysts towards ORR was studied by cyclic voltammetry, showing the higher electrochemical activity of FeE in comparison with FeD and the superior performance of catalysts supported on CNT rather than on Vulcan XC-72R carbon black. FeE/CNT was used as cathodic catalyst in a microbial fuel cell (MFC) using domestic wastewater as fuel. The maximum current density and power density recorded are 110 (mA m 2) and 127 0.9 (mW m 2), respectively. These values are comparable with those obtained using platinum on carbon Vulcan (0.13 mA m 2 and 226 0.2 mW m 2), demonstrating that these catalysts can be used as substitutes for commercial Pt/C.

Nguyen, M.t., D'Epifanio, A., Pepè Sciarria, T., Adani, F., Licoccia, S. (2014). Iron chelates as low-cost and effective electrocatalyst for oxygen reduction reaction in microbial fuel cells. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 39(12), 6462-6469 [10.1016/j.ijhydene.2014.02.064].

Iron chelates as low-cost and effective electrocatalyst for oxygen reduction reaction in microbial fuel cells

D'EPIFANIO, ALESSANDRA;LICOCCIA, SILVIA
2014-01-01

Abstract

Iron-chelated electrocatalysts for the oxygen reduction reaction (ORR) in a microbial fuel cell (MFC) were prepared from sodium ferric ethylenediamine-N,N0-bis(2- hydroxyphenylacetic acid) (FeE), sodium ferric diethylene triamine pentaacetic acid (FeD) supported on carbon Vulcan XC-72R carbon black and multi-walled carbon nanotubes (CNTs). Catalyst morphology was investigated by TEM; and the total surfaces areas as well as the pore volumes of catalysts were examined by nitrogen physisorption characterization. The catalytic activity of the iron based catalysts towards ORR was studied by cyclic voltammetry, showing the higher electrochemical activity of FeE in comparison with FeD and the superior performance of catalysts supported on CNT rather than on Vulcan XC-72R carbon black. FeE/CNT was used as cathodic catalyst in a microbial fuel cell (MFC) using domestic wastewater as fuel. The maximum current density and power density recorded are 110 (mA m 2) and 127 0.9 (mW m 2), respectively. These values are comparable with those obtained using platinum on carbon Vulcan (0.13 mA m 2 and 226 0.2 mW m 2), demonstrating that these catalysts can be used as substitutes for commercial Pt/C.
2014
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/07 - FONDAMENTI CHIMICI DELLE TECNOLOGIE
English
Con Impact Factor ISI
Iron-based catalyst; Iron chelates; Oxygen reduction reaction (ORR); Microbial fuel cell (MFC)
http://www.scopus.com/inward/record.url?eid=2-s2.0-84897408486&partnerID=40&md5=cd59c14f2dad8c5c857de227cf136604
Nguyen, M.t., D'Epifanio, A., Pepè Sciarria, T., Adani, F., Licoccia, S. (2014). Iron chelates as low-cost and effective electrocatalyst for oxygen reduction reaction in microbial fuel cells. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 39(12), 6462-6469 [10.1016/j.ijhydene.2014.02.064].
Nguyen, Mt; D'Epifanio, A; Pepè Sciarria, T; Adani, F; Licoccia, S
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
2014_IJHE_Toan.pdf

solo utenti autorizzati

Descrizione: articolo principale
Licenza: Copyright dell'editore
Dimensione 1.45 MB
Formato Adobe PDF
1.45 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/113703
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 61
  • ???jsp.display-item.citation.isi??? 59
social impact