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Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement

Ferroelectric functionalized dye-sensitized solar cells were fabricated by using a positively-poled LiNbO(3) substrate coated with ITO (ITO-LiNbO(3)) as a collector electrode and demonstrated enhanced power conversion efficiency. Surface potential properties of TiO(2) nanoparticle film coated on the...

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Autores principales: Liu, Xiaoyan, Zhang, Qifeng, Li, Jiangyu, Valanoor, Nagarajan, Tang, Xiao, Cao, Guozhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255840/
https://www.ncbi.nlm.nih.gov/pubmed/30478382
http://dx.doi.org/10.1038/s41598-018-35764-y
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author Liu, Xiaoyan
Zhang, Qifeng
Li, Jiangyu
Valanoor, Nagarajan
Tang, Xiao
Cao, Guozhong
author_facet Liu, Xiaoyan
Zhang, Qifeng
Li, Jiangyu
Valanoor, Nagarajan
Tang, Xiao
Cao, Guozhong
author_sort Liu, Xiaoyan
collection PubMed
description Ferroelectric functionalized dye-sensitized solar cells were fabricated by using a positively-poled LiNbO(3) substrate coated with ITO (ITO-LiNbO(3)) as a collector electrode and demonstrated enhanced power conversion efficiency. Surface potential properties of TiO(2) nanoparticle film coated on the ITO-LiNbO(3) (TiO(2)/ITO-LiNbO(3)) examined by Kelvin probe force microscopy (KPFM) confirmed that a large electric field (a few 10 V/µm) generated from LiNbO(3) can penetrate through the ITO layer and is applied to TiO(2) film. This polarization-induced electric field leads to an increased photocurrent density by attracting and promoting electrons to direct transport through the mesoporous TiO(2) network toward the collector electrode and a decreased charge recombination by facilitating electrons to pass through fewer boundaries of nanoparticles, resulting in high power conversion efficiency. The power conversion efficiency was enhanced by more than 40% in comparison with that without polarization-induced electric field. Incorporating functional ferroelectrics into photovoltaic cells would be a good strategy in improving photovoltaic performance and is applicable to other types of photovoltaic devices, such as perovskite solar cells.
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spelling pubmed-62558402018-12-03 Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement Liu, Xiaoyan Zhang, Qifeng Li, Jiangyu Valanoor, Nagarajan Tang, Xiao Cao, Guozhong Sci Rep Article Ferroelectric functionalized dye-sensitized solar cells were fabricated by using a positively-poled LiNbO(3) substrate coated with ITO (ITO-LiNbO(3)) as a collector electrode and demonstrated enhanced power conversion efficiency. Surface potential properties of TiO(2) nanoparticle film coated on the ITO-LiNbO(3) (TiO(2)/ITO-LiNbO(3)) examined by Kelvin probe force microscopy (KPFM) confirmed that a large electric field (a few 10 V/µm) generated from LiNbO(3) can penetrate through the ITO layer and is applied to TiO(2) film. This polarization-induced electric field leads to an increased photocurrent density by attracting and promoting electrons to direct transport through the mesoporous TiO(2) network toward the collector electrode and a decreased charge recombination by facilitating electrons to pass through fewer boundaries of nanoparticles, resulting in high power conversion efficiency. The power conversion efficiency was enhanced by more than 40% in comparison with that without polarization-induced electric field. Incorporating functional ferroelectrics into photovoltaic cells would be a good strategy in improving photovoltaic performance and is applicable to other types of photovoltaic devices, such as perovskite solar cells. Nature Publishing Group UK 2018-11-26 /pmc/articles/PMC6255840/ /pubmed/30478382 http://dx.doi.org/10.1038/s41598-018-35764-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Xiaoyan
Zhang, Qifeng
Li, Jiangyu
Valanoor, Nagarajan
Tang, Xiao
Cao, Guozhong
Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
title Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
title_full Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
title_fullStr Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
title_full_unstemmed Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
title_short Increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
title_sort increase of power conversion efficiency in dye-sensitized solar cells through ferroelectric substrate induced charge transport enhancement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255840/
https://www.ncbi.nlm.nih.gov/pubmed/30478382
http://dx.doi.org/10.1038/s41598-018-35764-y
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