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Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells

The ability to control the morphologies of active layers is a critical factor in the successful development of polymer solar cells (PSCs), and solvent processing additives offer a simple and effective way to accomplish this. In particular, diphenyl ether (DPE) is one of the most effective solvent ad...

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Autores principales: Park, Song Yi, Song, Seyeong, Yoon, Yung Jin, Lee, Tack Ho, An, Na Gyeong, Walker, Bright, Kim, Jin Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091327/
https://www.ncbi.nlm.nih.gov/pubmed/35558017
http://dx.doi.org/10.1039/c8ra08317g
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author Park, Song Yi
Song, Seyeong
Yoon, Yung Jin
Lee, Tack Ho
An, Na Gyeong
Walker, Bright
Kim, Jin Young
author_facet Park, Song Yi
Song, Seyeong
Yoon, Yung Jin
Lee, Tack Ho
An, Na Gyeong
Walker, Bright
Kim, Jin Young
author_sort Park, Song Yi
collection PubMed
description The ability to control the morphologies of active layers is a critical factor in the successful development of polymer solar cells (PSCs), and solvent processing additives offer a simple and effective way to accomplish this. In particular, diphenyl ether (DPE) is one of the most effective solvent additives but analogous additives based on this structure have not yet been extensively investigated. In this work, we have fabricated PSCs and investigated photovoltaic device characteristics using the series of non-halogenated, diphenyl-chalcogen solvent additives; DPE, diphenyl sulfide (DPS) and diphenyl selenide (DPSe). DPS devices showed optimal power conversion efficiencies (PCEs) of up to 9.08%, and DPE devices also showed similarly high PCEs of up to 8.85%. In contrast, DPSe devices showed relatively low PCEs (5.45% at best) which we attribute to significant surface recombination and high series resistance, which led to limited open-circuit voltage (V(OC)). In the case of DPS, fast, field-independent photocurrent saturation with negligible bimolecular recombination led to efficient charge separation and collection, which resulted in the highest PCEs. Additionally, using 1,2,4-trimethylbenzene and DPS as an entirely non-halogenated solvent/additive system, we successfully demonstrated device fabrication with comparably high PCEs of up to 8.4%. This work elucidates the effects of diphenyl-based solvent additives in PSCs and suggests a great potential of DPS as an effective non-halogenated solvent additive.
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spelling pubmed-90913272022-05-11 Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells Park, Song Yi Song, Seyeong Yoon, Yung Jin Lee, Tack Ho An, Na Gyeong Walker, Bright Kim, Jin Young RSC Adv Chemistry The ability to control the morphologies of active layers is a critical factor in the successful development of polymer solar cells (PSCs), and solvent processing additives offer a simple and effective way to accomplish this. In particular, diphenyl ether (DPE) is one of the most effective solvent additives but analogous additives based on this structure have not yet been extensively investigated. In this work, we have fabricated PSCs and investigated photovoltaic device characteristics using the series of non-halogenated, diphenyl-chalcogen solvent additives; DPE, diphenyl sulfide (DPS) and diphenyl selenide (DPSe). DPS devices showed optimal power conversion efficiencies (PCEs) of up to 9.08%, and DPE devices also showed similarly high PCEs of up to 8.85%. In contrast, DPSe devices showed relatively low PCEs (5.45% at best) which we attribute to significant surface recombination and high series resistance, which led to limited open-circuit voltage (V(OC)). In the case of DPS, fast, field-independent photocurrent saturation with negligible bimolecular recombination led to efficient charge separation and collection, which resulted in the highest PCEs. Additionally, using 1,2,4-trimethylbenzene and DPS as an entirely non-halogenated solvent/additive system, we successfully demonstrated device fabrication with comparably high PCEs of up to 8.4%. This work elucidates the effects of diphenyl-based solvent additives in PSCs and suggests a great potential of DPS as an effective non-halogenated solvent additive. The Royal Society of Chemistry 2018-11-28 /pmc/articles/PMC9091327/ /pubmed/35558017 http://dx.doi.org/10.1039/c8ra08317g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Park, Song Yi
Song, Seyeong
Yoon, Yung Jin
Lee, Tack Ho
An, Na Gyeong
Walker, Bright
Kim, Jin Young
Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
title Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
title_full Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
title_fullStr Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
title_full_unstemmed Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
title_short Non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
title_sort non-halogenated diphenyl-chalcogenide solvent processing additives for high-performance polymer bulk-heterojunction solar cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091327/
https://www.ncbi.nlm.nih.gov/pubmed/35558017
http://dx.doi.org/10.1039/c8ra08317g
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