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Neutron Diffraction Study of a Sintered Iron Electrode In Operando
[Image: see text] Iron is a promising, earth-abundant material for future energy applications. In this study, we use a neutron diffractometer to investigate the properties of an iron electrode in an alkaline environment. As neutrons penetrate deeply into materials, neutron scattering gives us a uniq...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350908/ https://www.ncbi.nlm.nih.gov/pubmed/34386149 http://dx.doi.org/10.1021/acs.jpcc.1c03263 |
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author | Weninger, Bernhard M. H. Thijs, Michel A. Nijman, Jeroen A. C. van Eijck, Lambert Mulder, Fokko M. |
author_facet | Weninger, Bernhard M. H. Thijs, Michel A. Nijman, Jeroen A. C. van Eijck, Lambert Mulder, Fokko M. |
author_sort | Weninger, Bernhard M. H. |
collection | PubMed |
description | [Image: see text] Iron is a promising, earth-abundant material for future energy applications. In this study, we use a neutron diffractometer to investigate the properties of an iron electrode in an alkaline environment. As neutrons penetrate deeply into materials, neutron scattering gives us a unique insight into what is happening inside the electrode. We made our measurements while the electrode was charging or discharging. Our key questions are: Which phases occur for the first and second discharge plateaus? And why are iron electrodes less responsive at higher discharge rates? We conclude that metallic iron and iron hydroxide form the redox pair for the first discharge plateau. For the second discharge plateau, we found a phase similar to feroxyhyte but with symmetrical and equally spaced arrangement of hydrogen atoms. The data suggest that no other iron oxide or iron (oxy)hydroxide formed. Remarkable findings include the following: (1) substantial amounts of iron hydroxide are always present inside the electrode. (2) Passivation is mostly caused by iron hydroxide that is unable to recharge. (3) Iron fractions change as expected, while iron hydroxide fractions are delayed, resulting in substantial amounts of amorphous, undetectable iron phases. About 40% of the participating iron of the first plateau and about 55% of the participating iron for the second plateau are undetectable. (4) Massive and unexpected precipitation of iron hydroxide occurs in the transition from discharging to charging. (2), (3), and (4) together cause accumulation of iron hydroxide inside the electrode. |
format | Online Article Text |
id | pubmed-8350908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83509082021-08-10 Neutron Diffraction Study of a Sintered Iron Electrode In Operando Weninger, Bernhard M. H. Thijs, Michel A. Nijman, Jeroen A. C. van Eijck, Lambert Mulder, Fokko M. J Phys Chem C Nanomater Interfaces [Image: see text] Iron is a promising, earth-abundant material for future energy applications. In this study, we use a neutron diffractometer to investigate the properties of an iron electrode in an alkaline environment. As neutrons penetrate deeply into materials, neutron scattering gives us a unique insight into what is happening inside the electrode. We made our measurements while the electrode was charging or discharging. Our key questions are: Which phases occur for the first and second discharge plateaus? And why are iron electrodes less responsive at higher discharge rates? We conclude that metallic iron and iron hydroxide form the redox pair for the first discharge plateau. For the second discharge plateau, we found a phase similar to feroxyhyte but with symmetrical and equally spaced arrangement of hydrogen atoms. The data suggest that no other iron oxide or iron (oxy)hydroxide formed. Remarkable findings include the following: (1) substantial amounts of iron hydroxide are always present inside the electrode. (2) Passivation is mostly caused by iron hydroxide that is unable to recharge. (3) Iron fractions change as expected, while iron hydroxide fractions are delayed, resulting in substantial amounts of amorphous, undetectable iron phases. About 40% of the participating iron of the first plateau and about 55% of the participating iron for the second plateau are undetectable. (4) Massive and unexpected precipitation of iron hydroxide occurs in the transition from discharging to charging. (2), (3), and (4) together cause accumulation of iron hydroxide inside the electrode. American Chemical Society 2021-07-23 2021-08-05 /pmc/articles/PMC8350908/ /pubmed/34386149 http://dx.doi.org/10.1021/acs.jpcc.1c03263 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Weninger, Bernhard M. H. Thijs, Michel A. Nijman, Jeroen A. C. van Eijck, Lambert Mulder, Fokko M. Neutron Diffraction Study of a Sintered Iron Electrode In Operando |
title | Neutron Diffraction Study of a Sintered Iron Electrode
In Operando |
title_full | Neutron Diffraction Study of a Sintered Iron Electrode
In Operando |
title_fullStr | Neutron Diffraction Study of a Sintered Iron Electrode
In Operando |
title_full_unstemmed | Neutron Diffraction Study of a Sintered Iron Electrode
In Operando |
title_short | Neutron Diffraction Study of a Sintered Iron Electrode
In Operando |
title_sort | neutron diffraction study of a sintered iron electrode
in operando |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350908/ https://www.ncbi.nlm.nih.gov/pubmed/34386149 http://dx.doi.org/10.1021/acs.jpcc.1c03263 |
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