High-efficiency ternary nonfullerene organic solar cells with record long-term thermal stability

Achieving high-efficiency organic solar cells (OSCs) with long-term thermal stability is a major challenge toward commercialization. In the present study, a ternary blend strategy was employed to improve the thermal stability of OSCs with a novel small molecular acceptor ITC6-2F serving as the secon...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 8; no. 43; pp. 2297 - 22917
Main Authors Zhang, Cai'e, Ming, Shouli, Wu, Hongbo, Wang, Xiaodong, Huang, Hao, Xue, Wenyue, Xu, Xinjun, Tang, Zheng, Ma, Wei, Bo, Zhishan
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 21.11.2020
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Abstract Achieving high-efficiency organic solar cells (OSCs) with long-term thermal stability is a major challenge toward commercialization. In the present study, a ternary blend strategy was employed to improve the thermal stability of OSCs with a novel small molecular acceptor ITC6-2F serving as the second acceptor. Compared with its parent compound ITC6-IC , the introduction of fluoro substituents at the two end groups can reduce the π-π stacking distance and enhance the intermolecular interactions in films. The PBDB-T : IDT-PDOT-C6 : ITC6-2F -based ternary blend film exhibits a reduced lamellar distance and an increased crystalline coherence length, compared to the corresponding binary blend films. Photo-physics and device physics analyses demonstrate that the charge-transfer state energy is dominated by PBDB-T and IDT-PDOT-C6 in the ternary OSCs. Also, ITC6-2F can facilitate the photonic energy transfer to IDT-PDOT-C6 and promote more excitons to reach the donor/acceptor (D/A) interfaces to achieve high-efficiency photoelectric conversion. More importantly, the enhanced intermolecular interactions and good miscibility between the two acceptors help to "freeze" the film morphology, leading to a significantly improved long-term thermal stability. The device efficiency remained at 80.3% of its initial value after 137 days of continuous heating at 75 °C in a nitrogen-filled glove box, which is a record result for high-efficiency OSCs reported so far. ITC6-2F as a third component in OSCs helps "freeze" the film morphology, leading to significantly improved long-term thermal stability.
AbstractList Achieving high-efficiency organic solar cells (OSCs) with long-term thermal stability is a major challenge toward commercialization. In the present study, a ternary blend strategy was employed to improve the thermal stability of OSCs with a novel small molecular acceptor ITC6-2F serving as the second acceptor. Compared with its parent compound ITC6-IC, the introduction of fluoro substituents at the two end groups can reduce the π–π stacking distance and enhance the intermolecular interactions in films. The PBDB-T:IDT-PDOT-C6:ITC6-2F-based ternary blend film exhibits a reduced lamellar distance and an increased crystalline coherence length, compared to the corresponding binary blend films. Photo-physics and device physics analyses demonstrate that the charge-transfer state energy is dominated by PBDB-T and IDT-PDOT-C6 in the ternary OSCs. Also, ITC6-2F can facilitate the photonic energy transfer to IDT-PDOT-C6 and promote more excitons to reach the donor/acceptor (D/A) interfaces to achieve high-efficiency photoelectric conversion. More importantly, the enhanced intermolecular interactions and good miscibility between the two acceptors help to “freeze” the film morphology, leading to a significantly improved long-term thermal stability. The device efficiency remained at 80.3% of its initial value after 137 days of continuous heating at 75 °C in a nitrogen-filled glove box, which is a record result for high-efficiency OSCs reported so far.
Achieving high-efficiency organic solar cells (OSCs) with long-term thermal stability is a major challenge toward commercialization. In the present study, a ternary blend strategy was employed to improve the thermal stability of OSCs with a novel small molecular acceptor ITC6-2F serving as the second acceptor. Compared with its parent compound ITC6-IC , the introduction of fluoro substituents at the two end groups can reduce the π–π stacking distance and enhance the intermolecular interactions in films. The PBDB-T : IDT-PDOT-C6 : ITC6-2F -based ternary blend film exhibits a reduced lamellar distance and an increased crystalline coherence length, compared to the corresponding binary blend films. Photo-physics and device physics analyses demonstrate that the charge-transfer state energy is dominated by PBDB-T and IDT-PDOT-C6 in the ternary OSCs. Also, ITC6-2F can facilitate the photonic energy transfer to IDT-PDOT-C6 and promote more excitons to reach the donor/acceptor (D/A) interfaces to achieve high-efficiency photoelectric conversion. More importantly, the enhanced intermolecular interactions and good miscibility between the two acceptors help to “freeze” the film morphology, leading to a significantly improved long-term thermal stability. The device efficiency remained at 80.3% of its initial value after 137 days of continuous heating at 75 °C in a nitrogen-filled glove box, which is a record result for high-efficiency OSCs reported so far.
Achieving high-efficiency organic solar cells (OSCs) with long-term thermal stability is a major challenge toward commercialization. In the present study, a ternary blend strategy was employed to improve the thermal stability of OSCs with a novel small molecular acceptor ITC6-2F serving as the second acceptor. Compared with its parent compound ITC6-IC , the introduction of fluoro substituents at the two end groups can reduce the π-π stacking distance and enhance the intermolecular interactions in films. The PBDB-T : IDT-PDOT-C6 : ITC6-2F -based ternary blend film exhibits a reduced lamellar distance and an increased crystalline coherence length, compared to the corresponding binary blend films. Photo-physics and device physics analyses demonstrate that the charge-transfer state energy is dominated by PBDB-T and IDT-PDOT-C6 in the ternary OSCs. Also, ITC6-2F can facilitate the photonic energy transfer to IDT-PDOT-C6 and promote more excitons to reach the donor/acceptor (D/A) interfaces to achieve high-efficiency photoelectric conversion. More importantly, the enhanced intermolecular interactions and good miscibility between the two acceptors help to "freeze" the film morphology, leading to a significantly improved long-term thermal stability. The device efficiency remained at 80.3% of its initial value after 137 days of continuous heating at 75 °C in a nitrogen-filled glove box, which is a record result for high-efficiency OSCs reported so far. ITC6-2F as a third component in OSCs helps "freeze" the film morphology, leading to significantly improved long-term thermal stability.
Author Xu, Xinjun
Bo, Zhishan
Ma, Wei
Xue, Wenyue
Zhang, Cai'e
Tang, Zheng
Wang, Xiaodong
Huang, Hao
Wu, Hongbo
Ming, Shouli
AuthorAffiliation Beijing Normal University
College of Chemistry
Donghua University
Center for Advanced Low-dimension Materials
State Key Laboratory for Mechanical Behavior of Materials
College of Materials Science and Engineering
Beijing Key Laboratory of Energy Conversion and Storage Materials
Xi'an Jiaotong University
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials
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– name: Donghua University
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Snippet Achieving high-efficiency organic solar cells (OSCs) with long-term thermal stability is a major challenge toward commercialization. In the present study, a...
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SubjectTerms Charge transfer
Coherence length
Commercialization
Efficiency
Energy charge
Energy conversion efficiency
Energy transfer
Excitons
Interfaces
Miscibility
Morphology
Photoelectricity
Photovoltaic cells
Physics
Solar cells
Thermal stability
Title High-efficiency ternary nonfullerene organic solar cells with record long-term thermal stability
URI https://www.proquest.com/docview/2458978776
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