Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells

To ensure long-term stable dye-sensitized solar cells (DSCs) and modules, a hermetic sealing is required. This research investigates the chemical stability of I-/I3- redox electrolyte and four different glass frits (GFs). Sintered GF layers were openly exposed to nonaqueous redox electrolyte and red...

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Main Authors: Katrine Flarup Jensen, Md. Mahbubur Rahman, Welmoed Veurman, Henning Brandt, Chan Im, Jürgen Wilde, Andreas Hinsch, Jae-Joon Lee
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:International Journal of Photoenergy
Online Access:http://dx.doi.org/10.1155/2013/696052
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author Katrine Flarup Jensen
Md. Mahbubur Rahman
Welmoed Veurman
Henning Brandt
Chan Im
Jürgen Wilde
Andreas Hinsch
Jae-Joon Lee
author_facet Katrine Flarup Jensen
Md. Mahbubur Rahman
Welmoed Veurman
Henning Brandt
Chan Im
Jürgen Wilde
Andreas Hinsch
Jae-Joon Lee
author_sort Katrine Flarup Jensen
collection DOAJ
description To ensure long-term stable dye-sensitized solar cells (DSCs) and modules, a hermetic sealing is required. This research investigates the chemical stability of I-/I3- redox electrolyte and four different glass frits (GFs). Sintered GF layers were openly exposed to nonaqueous redox electrolyte and redox electrolyte with 1, 5, and 10 wt% H2O in thin, encapsulated cells. The change in I3− absorbance was assigned to a reaction between the GF and I-/I3- electrolyte and was used to evaluate the chemical stability of the different GFs. The I3− absorbance change was monitored over 100 days. Two out of the four GFs were unstable when H2O was added to the redox electrolyte. The H2O caused metal ion leaching which was determined from EDX analysis of the inorganic remains of electrolyte samples. A GF based on Bi2O3–SiO2–B2O3 with low bond strength leached bismuth into electrolyte and formed the BiI3- complex. A ZnO–SiO2–Al2O3-based GF also became unstable when H2O was added to the redox electrolyte. Leaching of zinc ions due to exchange with H+ resulted in the formation of a zinc-iodine compound which caused I3− depletion. By applying the test design to different types of GFs, the material suitability in the DSC working environment was investigated.
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spelling doaj-art-e117a34b9fbd4f27bcf778db6a3546782025-08-20T03:26:00ZengWileyInternational Journal of Photoenergy1110-662X1687-529X2013-01-01201310.1155/2013/696052696052Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar CellsKatrine Flarup Jensen0Md. Mahbubur Rahman1Welmoed Veurman2Henning Brandt3Chan Im4Jürgen Wilde5Andreas Hinsch6Jae-Joon Lee7Fraunhofer Institute for Solar Energy Systems (ISE), HeidenhofstraBe 2, 79110 Freiburg, GermanyDepartment of Advanced Technology Fusion, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 143-701, Republic of KoreaFraunhofer Institute for Solar Energy Systems (ISE), HeidenhofstraBe 2, 79110 Freiburg, GermanyFraunhofer Institute for Solar Energy Systems (ISE), HeidenhofstraBe 2, 79110 Freiburg, GermanyKonkuk University-Fraunhofer Next Generation Solar Cell Research Center (KFnSC), 120 Neungdong-ro, Gwangjin-gu, Seoul 143-701, Republic of KoreaDepartment of Microsystems Engineering-IMTEK, University of Freiburg, Georges-Köhler-Allee 103, 79110 Freiburg, GermanyFraunhofer Institute for Solar Energy Systems (ISE), HeidenhofstraBe 2, 79110 Freiburg, GermanyKonkuk University-Fraunhofer Next Generation Solar Cell Research Center (KFnSC), 120 Neungdong-ro, Gwangjin-gu, Seoul 143-701, Republic of KoreaTo ensure long-term stable dye-sensitized solar cells (DSCs) and modules, a hermetic sealing is required. This research investigates the chemical stability of I-/I3- redox electrolyte and four different glass frits (GFs). Sintered GF layers were openly exposed to nonaqueous redox electrolyte and redox electrolyte with 1, 5, and 10 wt% H2O in thin, encapsulated cells. The change in I3− absorbance was assigned to a reaction between the GF and I-/I3- electrolyte and was used to evaluate the chemical stability of the different GFs. The I3− absorbance change was monitored over 100 days. Two out of the four GFs were unstable when H2O was added to the redox electrolyte. The H2O caused metal ion leaching which was determined from EDX analysis of the inorganic remains of electrolyte samples. A GF based on Bi2O3–SiO2–B2O3 with low bond strength leached bismuth into electrolyte and formed the BiI3- complex. A ZnO–SiO2–Al2O3-based GF also became unstable when H2O was added to the redox electrolyte. Leaching of zinc ions due to exchange with H+ resulted in the formation of a zinc-iodine compound which caused I3− depletion. By applying the test design to different types of GFs, the material suitability in the DSC working environment was investigated.http://dx.doi.org/10.1155/2013/696052
spellingShingle Katrine Flarup Jensen
Md. Mahbubur Rahman
Welmoed Veurman
Henning Brandt
Chan Im
Jürgen Wilde
Andreas Hinsch
Jae-Joon Lee
Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells
International Journal of Photoenergy
title Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells
title_full Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells
title_fullStr Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells
title_full_unstemmed Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells
title_short Glass Frit Dissolution Influenced by Material Composition and the Water Content in Iodide/Triiodide Electrolyte of Dye-Sensitized Solar Cells
title_sort glass frit dissolution influenced by material composition and the water content in iodide triiodide electrolyte of dye sensitized solar cells
url http://dx.doi.org/10.1155/2013/696052
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