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Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells
Hybrid organic-inorganic halide perovskites are low-cost solution-processable solar cell materials with photovoltaic properties that rival those of crystalline silicon. The perovskite films are typically sandwiched between thin layers of hole and electron transport materials, which efficiently extra...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606993/ https://www.ncbi.nlm.nih.gov/pubmed/28931833 http://dx.doi.org/10.1038/s41467-017-00588-3 |
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author | Lin, Xiongfeng Jumabekov, Askhat N. Lal, Niraj N. Pascoe, Alexander R. Gómez, Daniel E. Duffy, Noel W. Chesman, Anthony S. R. Sears, Kallista Fournier, Maxime Zhang, Yupeng Bao, Qiaoliang Cheng, Yi-Bing Spiccia, Leone Bach, Udo |
author_facet | Lin, Xiongfeng Jumabekov, Askhat N. Lal, Niraj N. Pascoe, Alexander R. Gómez, Daniel E. Duffy, Noel W. Chesman, Anthony S. R. Sears, Kallista Fournier, Maxime Zhang, Yupeng Bao, Qiaoliang Cheng, Yi-Bing Spiccia, Leone Bach, Udo |
author_sort | Lin, Xiongfeng |
collection | PubMed |
description | Hybrid organic-inorganic halide perovskites are low-cost solution-processable solar cell materials with photovoltaic properties that rival those of crystalline silicon. The perovskite films are typically sandwiched between thin layers of hole and electron transport materials, which efficiently extract photogenerated charges. This affords high-energy conversion efficiencies but results in significant performance and fabrication challenges. Herein we present a simple charge transport layer-free perovskite solar cell, comprising only a perovskite layer with two interdigitated gold back-contacts. Charge extraction is achieved via self-assembled monolayers and their associated dipole fields at the metal-perovskite interface. Photovoltages of ~600 mV generated by self-assembled molecular monolayer modified perovskite solar cells are equivalent to the built-in potential generated by individual dipole layers. Efficient charge extraction results in photocurrents of up to 12.1 mA cm(−2) under simulated sunlight, despite a large electrode spacing. |
format | Online Article Text |
id | pubmed-5606993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56069932017-09-22 Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells Lin, Xiongfeng Jumabekov, Askhat N. Lal, Niraj N. Pascoe, Alexander R. Gómez, Daniel E. Duffy, Noel W. Chesman, Anthony S. R. Sears, Kallista Fournier, Maxime Zhang, Yupeng Bao, Qiaoliang Cheng, Yi-Bing Spiccia, Leone Bach, Udo Nat Commun Article Hybrid organic-inorganic halide perovskites are low-cost solution-processable solar cell materials with photovoltaic properties that rival those of crystalline silicon. The perovskite films are typically sandwiched between thin layers of hole and electron transport materials, which efficiently extract photogenerated charges. This affords high-energy conversion efficiencies but results in significant performance and fabrication challenges. Herein we present a simple charge transport layer-free perovskite solar cell, comprising only a perovskite layer with two interdigitated gold back-contacts. Charge extraction is achieved via self-assembled monolayers and their associated dipole fields at the metal-perovskite interface. Photovoltages of ~600 mV generated by self-assembled molecular monolayer modified perovskite solar cells are equivalent to the built-in potential generated by individual dipole layers. Efficient charge extraction results in photocurrents of up to 12.1 mA cm(−2) under simulated sunlight, despite a large electrode spacing. Nature Publishing Group UK 2017-09-20 /pmc/articles/PMC5606993/ /pubmed/28931833 http://dx.doi.org/10.1038/s41467-017-00588-3 Text en © The Author(s) 2017 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 Lin, Xiongfeng Jumabekov, Askhat N. Lal, Niraj N. Pascoe, Alexander R. Gómez, Daniel E. Duffy, Noel W. Chesman, Anthony S. R. Sears, Kallista Fournier, Maxime Zhang, Yupeng Bao, Qiaoliang Cheng, Yi-Bing Spiccia, Leone Bach, Udo Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
title | Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
title_full | Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
title_fullStr | Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
title_full_unstemmed | Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
title_short | Dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
title_sort | dipole-field-assisted charge extraction in metal-perovskite-metal back-contact solar cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606993/ https://www.ncbi.nlm.nih.gov/pubmed/28931833 http://dx.doi.org/10.1038/s41467-017-00588-3 |
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