Cargando…
Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors
OBJECTIVE: Palladised cells of Desulfovibrio desulfuricans and Shewanella oneidensis have been reported as fuel cell electrocatalysts but growth at scale may be unattractive/costly; we have evaluated the potential of using E. coli, using H(2)/formate for Pd-nanoparticle manufacture. RESULTS: Using ‘...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055570/ https://www.ncbi.nlm.nih.gov/pubmed/27502834 http://dx.doi.org/10.1007/s10529-016-2183-3 |
_version_ | 1782458779697152000 |
---|---|
author | Courtney, J. Deplanche, K. Rees, N. V. Macaskie, L. E. |
author_facet | Courtney, J. Deplanche, K. Rees, N. V. Macaskie, L. E. |
author_sort | Courtney, J. |
collection | PubMed |
description | OBJECTIVE: Palladised cells of Desulfovibrio desulfuricans and Shewanella oneidensis have been reported as fuel cell electrocatalysts but growth at scale may be unattractive/costly; we have evaluated the potential of using E. coli, using H(2)/formate for Pd-nanoparticle manufacture. RESULTS: Using ‘bio-Pd’ made under H(2) (20 wt%) cyclic voltammograms suggested electrochemical activity of bio-NPs in a native state, attributed to proton adsorption/desorption. Bio-Pd prepared using formate as the electron donor gave smaller, well separated NPs; this material showed no electrochemical properties, and hence little potential for fuel cell use using a simple preparation technique. Bio-Pd on S. oneidensis gave similar results to those obtained using E. coli. CONCLUSION: Bio-Pd is sufficiently conductive to make an E. coli-derived electrochemically active material on intact, unprocessed bacterial cells if prepared at the expense of H(2), showing potential for fuel cell applications using a simple one-step preparation method. |
format | Online Article Text |
id | pubmed-5055570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-50555702016-10-26 Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors Courtney, J. Deplanche, K. Rees, N. V. Macaskie, L. E. Biotechnol Lett Original Research Paper OBJECTIVE: Palladised cells of Desulfovibrio desulfuricans and Shewanella oneidensis have been reported as fuel cell electrocatalysts but growth at scale may be unattractive/costly; we have evaluated the potential of using E. coli, using H(2)/formate for Pd-nanoparticle manufacture. RESULTS: Using ‘bio-Pd’ made under H(2) (20 wt%) cyclic voltammograms suggested electrochemical activity of bio-NPs in a native state, attributed to proton adsorption/desorption. Bio-Pd prepared using formate as the electron donor gave smaller, well separated NPs; this material showed no electrochemical properties, and hence little potential for fuel cell use using a simple preparation technique. Bio-Pd on S. oneidensis gave similar results to those obtained using E. coli. CONCLUSION: Bio-Pd is sufficiently conductive to make an E. coli-derived electrochemically active material on intact, unprocessed bacterial cells if prepared at the expense of H(2), showing potential for fuel cell applications using a simple one-step preparation method. Springer Netherlands 2016-08-08 2016 /pmc/articles/PMC5055570/ /pubmed/27502834 http://dx.doi.org/10.1007/s10529-016-2183-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Paper Courtney, J. Deplanche, K. Rees, N. V. Macaskie, L. E. Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors |
title | Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors |
title_full | Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors |
title_fullStr | Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors |
title_full_unstemmed | Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors |
title_short | Biomanufacture of nano-Pd(0) by Escherichia coli and electrochemical activity of bio-Pd(0) made at the expense of H(2) and formate as electron donors |
title_sort | biomanufacture of nano-pd(0) by escherichia coli and electrochemical activity of bio-pd(0) made at the expense of h(2) and formate as electron donors |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055570/ https://www.ncbi.nlm.nih.gov/pubmed/27502834 http://dx.doi.org/10.1007/s10529-016-2183-3 |
work_keys_str_mv | AT courtneyj biomanufactureofnanopd0byescherichiacoliandelectrochemicalactivityofbiopd0madeattheexpenseofh2andformateaselectrondonors AT deplanchek biomanufactureofnanopd0byescherichiacoliandelectrochemicalactivityofbiopd0madeattheexpenseofh2andformateaselectrondonors AT reesnv biomanufactureofnanopd0byescherichiacoliandelectrochemicalactivityofbiopd0madeattheexpenseofh2andformateaselectrondonors AT macaskiele biomanufactureofnanopd0byescherichiacoliandelectrochemicalactivityofbiopd0madeattheexpenseofh2andformateaselectrondonors |