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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...

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Autores principales: Walch, Gregor, Rotter, Bernhard, Brunauer, Georg Christoph, Esmaeili, Esmaeil, Opitz, Alexander Karl, Kubicek, Markus, Summhammer, Johann, Ponweiser, Karl, Fleig, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
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.
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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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