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Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte
An environmentally friendly solid-state quantum dot sensitized solar cell (ss-QDSSC) was prepared by combining colloidal SnS QDs as the sensitizer and organic hole scavenger spiro-OMeTAD (2,2′,7,7′-tetrakis-(N,N-di-p-methoxyphenylamine)9,9′-spirobifluorene) as the solid-state electrolyte, and the en...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090527/ https://www.ncbi.nlm.nih.gov/pubmed/27877682 http://dx.doi.org/10.1088/1468-6996/15/3/035006 |
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author | Oda, Yoshiaki Shen, Heping Zhao, Lin Li, Jianbao Iwamoto, Mitsumasa Lin, Hong |
author_facet | Oda, Yoshiaki Shen, Heping Zhao, Lin Li, Jianbao Iwamoto, Mitsumasa Lin, Hong |
author_sort | Oda, Yoshiaki |
collection | PubMed |
description | An environmentally friendly solid-state quantum dot sensitized solar cell (ss-QDSSC) was prepared by combining colloidal SnS QDs as the sensitizer and organic hole scavenger spiro-OMeTAD (2,2′,7,7′-tetrakis-(N,N-di-p-methoxyphenylamine)9,9′-spirobifluorene) as the solid-state electrolyte, and the energy alignment of SnS and TiO(2) was investigated. The bandgap of colloidal SnS QDs increased with decreasing particle size from 14 to 4 nm due to an upshift of the conduction band and a downshift of the valence band. In TiO(2)/SnS heterojunctions, the conduction band minimum (CBM) difference between TiO(2) and SnS was as large as ∼0.8 eV; this difference decreased with decreasing particle size, but was sufficient for electron injection from SnS nanoparticles of any size into TiO(2). Meanwhile, the sensitizer regeneration driving force, that is, the difference between the valence band maximum (VBM) of SnS and the work function of the electrolyte, showed an opposite behaviour with the SnS size due to a downward shift of the SnS VB. Consequently, smaller SnS QDs should result in a more efficient charge transfer in heterojunctions, revealing the advantages of QDs vs larger particles as sensitizers. This prediction was confirmed by the improved photovoltaic performance of ss-QDSSCs modified with SnS nanoparticles, which peaked for 5–6 nm sized SnS nanoparticles due to the balance between electron injection and sunlight absorption. |
format | Online Article Text |
id | pubmed-5090527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-50905272016-11-22 Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte Oda, Yoshiaki Shen, Heping Zhao, Lin Li, Jianbao Iwamoto, Mitsumasa Lin, Hong Sci Technol Adv Mater Papers An environmentally friendly solid-state quantum dot sensitized solar cell (ss-QDSSC) was prepared by combining colloidal SnS QDs as the sensitizer and organic hole scavenger spiro-OMeTAD (2,2′,7,7′-tetrakis-(N,N-di-p-methoxyphenylamine)9,9′-spirobifluorene) as the solid-state electrolyte, and the energy alignment of SnS and TiO(2) was investigated. The bandgap of colloidal SnS QDs increased with decreasing particle size from 14 to 4 nm due to an upshift of the conduction band and a downshift of the valence band. In TiO(2)/SnS heterojunctions, the conduction band minimum (CBM) difference between TiO(2) and SnS was as large as ∼0.8 eV; this difference decreased with decreasing particle size, but was sufficient for electron injection from SnS nanoparticles of any size into TiO(2). Meanwhile, the sensitizer regeneration driving force, that is, the difference between the valence band maximum (VBM) of SnS and the work function of the electrolyte, showed an opposite behaviour with the SnS size due to a downward shift of the SnS VB. Consequently, smaller SnS QDs should result in a more efficient charge transfer in heterojunctions, revealing the advantages of QDs vs larger particles as sensitizers. This prediction was confirmed by the improved photovoltaic performance of ss-QDSSCs modified with SnS nanoparticles, which peaked for 5–6 nm sized SnS nanoparticles due to the balance between electron injection and sunlight absorption. Taylor & Francis 2014-06-10 /pmc/articles/PMC5090527/ /pubmed/27877682 http://dx.doi.org/10.1088/1468-6996/15/3/035006 Text en © 2014 National Institute for Materials Science http://creativecommons.org/licenses/by-nc-sa/3.0/ Content from this work may be used under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 licence (http://creativecommons.org/licenses/by-nc-sa/3.0/) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI. |
spellingShingle | Papers Oda, Yoshiaki Shen, Heping Zhao, Lin Li, Jianbao Iwamoto, Mitsumasa Lin, Hong Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte |
title | Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte |
title_full | Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte |
title_fullStr | Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte |
title_full_unstemmed | Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte |
title_short | Energetic alignment in nontoxic SnS quantum dot-sensitized solar cell employing spiro-OMeTAD as the solid-state electrolyte |
title_sort | energetic alignment in nontoxic sns quantum dot-sensitized solar cell employing spiro-ometad as the solid-state electrolyte |
topic | Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090527/ https://www.ncbi.nlm.nih.gov/pubmed/27877682 http://dx.doi.org/10.1088/1468-6996/15/3/035006 |
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