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A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes
A single crystalline SrTiO(3) working electrode in a zirconia-based solid oxide electrochemical cell is illuminated by UV light at temperatures of 360–460 °C. In addition to photovoltaic effects, this leads to the build-up of a battery-type voltage up to more than 300 mV. After switching off UV ligh...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315022/ https://www.ncbi.nlm.nih.gov/pubmed/28261480 http://dx.doi.org/10.1039/c6ta08110j |
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author | Walch, Gregor Rotter, Bernhard Brunauer, Georg Christoph Esmaeili, Esmaeil Opitz, Alexander Karl Kubicek, Markus Summhammer, Johann Ponweiser, Karl Fleig, Jürgen |
author_facet | Walch, Gregor Rotter, Bernhard Brunauer, Georg Christoph Esmaeili, Esmaeil Opitz, Alexander Karl Kubicek, Markus Summhammer, Johann Ponweiser, Karl Fleig, Jürgen |
author_sort | Walch, Gregor |
collection | PubMed |
description | A single crystalline SrTiO(3) working electrode in a zirconia-based solid oxide electrochemical cell is illuminated by UV light at temperatures of 360–460 °C. In addition to photovoltaic effects, this leads to the build-up of a battery-type voltage up to more than 300 mV. After switching off UV light, this voltage only slowly decays. It is caused by UV-induced oxygen incorporation into the mixed conducting working electrode and thus by changes of the oxygen stoichiometry δ in SrTiO(3–δ) under UV illumination. These changes of the oxygen content could be followed in time-dependent voltage measurements and also manifest themselves in time-dependent resistance changes during and after UV illumination. Discharge currents measured after UV illumination reveal that a large fraction of the existing oxygen vacancies in SrTiO(3) become filled under UV light. Additional measurements on cells with TiO(2) thin film electrodes show the broader applicability of this novel approach for transforming light into chemical energy and thus the feasibility of solid oxide photoelectrochemical cells (SOPECs) in general and of a “light-charged oxygen battery” in particular. |
format | Online Article Text |
id | pubmed-5315022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-53150222017-03-01 A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes Walch, Gregor Rotter, Bernhard Brunauer, Georg Christoph Esmaeili, Esmaeil Opitz, Alexander Karl Kubicek, Markus Summhammer, Johann Ponweiser, Karl Fleig, Jürgen J Mater Chem A Mater Energy Sustain Chemistry A single crystalline SrTiO(3) working electrode in a zirconia-based solid oxide electrochemical cell is illuminated by UV light at temperatures of 360–460 °C. In addition to photovoltaic effects, this leads to the build-up of a battery-type voltage up to more than 300 mV. After switching off UV light, this voltage only slowly decays. It is caused by UV-induced oxygen incorporation into the mixed conducting working electrode and thus by changes of the oxygen stoichiometry δ in SrTiO(3–δ) under UV illumination. These changes of the oxygen content could be followed in time-dependent voltage measurements and also manifest themselves in time-dependent resistance changes during and after UV illumination. Discharge currents measured after UV illumination reveal that a large fraction of the existing oxygen vacancies in SrTiO(3) become filled under UV light. Additional measurements on cells with TiO(2) thin film electrodes show the broader applicability of this novel approach for transforming light into chemical energy and thus the feasibility of solid oxide photoelectrochemical cells (SOPECs) in general and of a “light-charged oxygen battery” in particular. Royal Society of Chemistry 2017-01-28 2016-12-12 /pmc/articles/PMC5315022/ /pubmed/28261480 http://dx.doi.org/10.1039/c6ta08110j Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Walch, Gregor Rotter, Bernhard Brunauer, Georg Christoph Esmaeili, Esmaeil Opitz, Alexander Karl Kubicek, Markus Summhammer, Johann Ponweiser, Karl Fleig, Jürgen A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes |
title | A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes |
title_full | A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes |
title_fullStr | A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes |
title_full_unstemmed | A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes |
title_short | A solid oxide photoelectrochemical cell with UV light-driven oxygen storage in mixed conducting electrodes |
title_sort | solid oxide photoelectrochemical cell with uv light-driven oxygen storage in mixed conducting electrodes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315022/ https://www.ncbi.nlm.nih.gov/pubmed/28261480 http://dx.doi.org/10.1039/c6ta08110j |
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