Conference Paper: Impact of salinity on cathode catalyst performance in microbial fuel cells (MFCs)
| Title | Impact of salinity on cathode catalyst performance in microbial fuel cells (MFCs) |
|---|---|
| Authors | Wang, X1 Cheng, S2 3 Zhang, X4 Li, XY1 Logan, BE3 |
| Keywords | Cathode Chloride Microbial Fuel Cell Salinity |
| Issue Date | 2011 |
| Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/ijhydene |
| Citation | International Journal of Hydrogen Energy, 2011, v. 36 n. 21, p. 13900-13906 [How to Cite?] DOI: http://dx.doi.org/10.1016/j.ijhydene.2011.03.052 |
| Abstract | Several alternative cathode catalysts have been proposed for microbial fuel cells (MFCs), but effects of salinity (sodium chloride) on catalyst performance, separate from those of conductivity on internal resistance, have not been previously examined. Three different types of cathode materials were tested here with increasingly saline solutions using single-chamber, air-cathode MFCs. The best MFC performance was obtained using a Co catalyst (cobalt tetramethoxyphenyl porphyrin; CoTMPP), with power increasing by 24 ± 1% to 1062 ± 9 mW/m 2 (normalized to the projected cathode surface area) when 250 mM NaCl (final conductivity of 31.3 mS/cm) was added (initial conductivity of 7.5 mS/cm). This power density was 25 ± 1% higher than that achieved with Pt on carbon cloth, and 27 ± 1% more than that produced using an activated carbon/nickel mesh (AC) cathode in the highest salinity solution. Linear sweep voltammetry (LSV) was used to separate changes in performance due to solution conductivity from those produced by reductions in ohmic resistance with the higher conductivity solutions. The potential of the cathode with CoTMPP increased by 17-20 mV in LSVs when the NaCl addition was increased from 0 to 250 mM independent of solution conductivity changes. Increases in current were observed with salinity increases in LSVs for AC, but not for Pt cathodes. Cathodes with CoTMPP had increased catalytic activity at higher salt concentrations in cyclic voltammograms compared to Pt and AC. These results suggest that special consideration should be given to the type of catalyst used with more saline wastewaters. While Pt oxygen reduction activity is reduced, CoTMPP cathode performance will be improved at higher salt concentrations expected for wastewaters containing seawater. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved. |
| ISSN | 0360-3199 2011 Impact Factor: 4.054 2011 SCImago Journal Rankings: 0.210 |
| DOI | http://dx.doi.org/10.1016/j.ijhydene.2011.03.052 |
| ISI Accession Number ID | WOS:000296208800068 |
| References | References in Scopus |
| dc.contributor.author | Wang, X |
|---|---|
| dc.contributor.author | Cheng, S |
| dc.contributor.author | Zhang, X |
| dc.contributor.author | Li, XY |
| dc.contributor.author | Logan, BE |
| dc.date.accessioned | 2012-06-26T06:35:54Z |
| dc.date.available | 2012-06-26T06:35:54Z |
| dc.date.issued | 2011 |
| dc.description.abstract | Several alternative cathode catalysts have been proposed for microbial fuel cells (MFCs), but effects of salinity (sodium chloride) on catalyst performance, separate from those of conductivity on internal resistance, have not been previously examined. Three different types of cathode materials were tested here with increasingly saline solutions using single-chamber, air-cathode MFCs. The best MFC performance was obtained using a Co catalyst (cobalt tetramethoxyphenyl porphyrin; CoTMPP), with power increasing by 24 ± 1% to 1062 ± 9 mW/m 2 (normalized to the projected cathode surface area) when 250 mM NaCl (final conductivity of 31.3 mS/cm) was added (initial conductivity of 7.5 mS/cm). This power density was 25 ± 1% higher than that achieved with Pt on carbon cloth, and 27 ± 1% more than that produced using an activated carbon/nickel mesh (AC) cathode in the highest salinity solution. Linear sweep voltammetry (LSV) was used to separate changes in performance due to solution conductivity from those produced by reductions in ohmic resistance with the higher conductivity solutions. The potential of the cathode with CoTMPP increased by 17-20 mV in LSVs when the NaCl addition was increased from 0 to 250 mM independent of solution conductivity changes. Increases in current were observed with salinity increases in LSVs for AC, but not for Pt cathodes. Cathodes with CoTMPP had increased catalytic activity at higher salt concentrations in cyclic voltammograms compared to Pt and AC. These results suggest that special consideration should be given to the type of catalyst used with more saline wastewaters. While Pt oxygen reduction activity is reduced, CoTMPP cathode performance will be improved at higher salt concentrations expected for wastewaters containing seawater. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved. |
| dc.description.nature | Link_to_subscribed_fulltext |
| dc.identifier.citation | International Journal of Hydrogen Energy, 2011, v. 36 n. 21, p. 13900-13906 [How to Cite?] DOI: http://dx.doi.org/10.1016/j.ijhydene.2011.03.052 |
| dc.identifier.doi | http://dx.doi.org/10.1016/j.ijhydene.2011.03.052 |
| dc.identifier.epage | 13906 |
| dc.identifier.hkuros | 209074 |
| dc.identifier.isi | WOS:000296208800068 |
| dc.identifier.issn | 0360-3199 2011 Impact Factor: 4.054 2011 SCImago Journal Rankings: 0.210 |
| dc.identifier.issue | 21 |
| dc.identifier.scopus | eid_2-s2.0-80755173481 |
| dc.identifier.spage | 13900 |
| dc.identifier.uri | http://hdl.handle.net/10722/152178 |
| dc.identifier.volume | 36 |
| dc.language | eng |
| dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/ijhydene |
| dc.publisher.place | United Kingdom |
| dc.relation.ispartof | International Journal of Hydrogen Energy |
| dc.relation.references | References in Scopus |
| dc.subject | Cathode |
| dc.subject | Chloride |
| dc.subject | Microbial Fuel Cell |
| dc.subject | Salinity |
| dc.title | Impact of salinity on cathode catalyst performance in microbial fuel cells (MFCs) |
| dc.type | Conference_Paper |
Author Affiliations
- The University of Hong Kong
- Zhejiang University
- Pennsylvania State University
- Tsinghua University

