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Crystallization driven boost in fill factor and stability in additive-free organic solar cells

The control of morphology and microstructure during and after the active layer processing of bulk-heterojunction solar cells is critical to obtain elevated fill factors and overall good device performance. With the recent development of non-fullerene acceptors, wide attention has been paid to improv...

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Autores principales: Garcia Romero, David, Di Mario, Lorenzo, Portale, Giuseppe, Loi, Maria Antonietta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562594/
https://www.ncbi.nlm.nih.gov/pubmed/34765223
http://dx.doi.org/10.1039/d1ta08232a
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author Garcia Romero, David
Di Mario, Lorenzo
Portale, Giuseppe
Loi, Maria Antonietta
author_facet Garcia Romero, David
Di Mario, Lorenzo
Portale, Giuseppe
Loi, Maria Antonietta
author_sort Garcia Romero, David
collection PubMed
description The control of morphology and microstructure during and after the active layer processing of bulk-heterojunction solar cells is critical to obtain elevated fill factors and overall good device performance. With the recent development of non-fullerene acceptors, wide attention has been paid to improve miscibility, solubility and nanoscale separation by laborious molecular design processes and by the use of additives. Nonetheless, several post-processing strategies can equally contribute to obtain an optimum phase separation and even to an enhanced crystallinity, but their effect on performance and device lifetime of polymer/non-fullerene acceptor solar cells is still unclear. Herein, we report a systematic comparison between different post-processing treatments including thermal annealing (TA), vacuum drying (VD) and solvent vapor annealing (SVA) on the TPD-3F polymer and IT-4F non-fullerene acceptor, comparing their effects on device performance as well as on the morphology and optical and electrical properties. The optimized SVA treated devices exhibited power conversion efficiencies close to 14% with a remarkable 76% fill factor and superior short-circuit currents compared to the one of untreated devices. Moreover, SVA demonstrated improvements in device stability both under illumination and under ambient conditions. The induced phase separation and the increased crystallinity of the acceptor molecules, as revealed by GIWAXS measurements, led to increased photogenerated currents, with a more effective exciton dissociation and charge collection. The open-circuit voltage losses in the SVA and TA devices were explained by a bandgap reduction and a higher trap-assisted recombination, respectively. Overall, our study points to the role of post-processing in organic solar cell fabrication, and contributes towards a new generation of efficient and stable additive-free organic solar cells.
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spelling pubmed-85625942021-11-09 Crystallization driven boost in fill factor and stability in additive-free organic solar cells Garcia Romero, David Di Mario, Lorenzo Portale, Giuseppe Loi, Maria Antonietta J Mater Chem A Mater Chemistry The control of morphology and microstructure during and after the active layer processing of bulk-heterojunction solar cells is critical to obtain elevated fill factors and overall good device performance. With the recent development of non-fullerene acceptors, wide attention has been paid to improve miscibility, solubility and nanoscale separation by laborious molecular design processes and by the use of additives. Nonetheless, several post-processing strategies can equally contribute to obtain an optimum phase separation and even to an enhanced crystallinity, but their effect on performance and device lifetime of polymer/non-fullerene acceptor solar cells is still unclear. Herein, we report a systematic comparison between different post-processing treatments including thermal annealing (TA), vacuum drying (VD) and solvent vapor annealing (SVA) on the TPD-3F polymer and IT-4F non-fullerene acceptor, comparing their effects on device performance as well as on the morphology and optical and electrical properties. The optimized SVA treated devices exhibited power conversion efficiencies close to 14% with a remarkable 76% fill factor and superior short-circuit currents compared to the one of untreated devices. Moreover, SVA demonstrated improvements in device stability both under illumination and under ambient conditions. The induced phase separation and the increased crystallinity of the acceptor molecules, as revealed by GIWAXS measurements, led to increased photogenerated currents, with a more effective exciton dissociation and charge collection. The open-circuit voltage losses in the SVA and TA devices were explained by a bandgap reduction and a higher trap-assisted recombination, respectively. Overall, our study points to the role of post-processing in organic solar cell fabrication, and contributes towards a new generation of efficient and stable additive-free organic solar cells. The Royal Society of Chemistry 2021-10-11 /pmc/articles/PMC8562594/ /pubmed/34765223 http://dx.doi.org/10.1039/d1ta08232a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Garcia Romero, David
Di Mario, Lorenzo
Portale, Giuseppe
Loi, Maria Antonietta
Crystallization driven boost in fill factor and stability in additive-free organic solar cells
title Crystallization driven boost in fill factor and stability in additive-free organic solar cells
title_full Crystallization driven boost in fill factor and stability in additive-free organic solar cells
title_fullStr Crystallization driven boost in fill factor and stability in additive-free organic solar cells
title_full_unstemmed Crystallization driven boost in fill factor and stability in additive-free organic solar cells
title_short Crystallization driven boost in fill factor and stability in additive-free organic solar cells
title_sort crystallization driven boost in fill factor and stability in additive-free organic solar cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562594/
https://www.ncbi.nlm.nih.gov/pubmed/34765223
http://dx.doi.org/10.1039/d1ta08232a
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