Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency

Abstract Non-fullerene acceptors (NFAs) play a crucial role in enhancing the performance of bulk heterojunction organic solar cells (BHJ-OSCs). Therefore, new A–π–D–π–A configured NFAs (BDTD1-BDTD7) were developed from BDTR reference through terminal modification with benzothiophene (BT) based accep...

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Main Authors: Mashal Khan, Maria Zafar, Zafar Ullah, Iqra Shafiq, Saifullah Bullo, Tansir Ahamad, Ke Chen
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-11718-z
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author Mashal Khan
Maria Zafar
Zafar Ullah
Iqra Shafiq
Saifullah Bullo
Tansir Ahamad
Ke Chen
author_facet Mashal Khan
Maria Zafar
Zafar Ullah
Iqra Shafiq
Saifullah Bullo
Tansir Ahamad
Ke Chen
author_sort Mashal Khan
collection DOAJ
description Abstract Non-fullerene acceptors (NFAs) play a crucial role in enhancing the performance of bulk heterojunction organic solar cells (BHJ-OSCs). Therefore, new A–π–D–π–A configured NFAs (BDTD1-BDTD7) were developed from BDTR reference through terminal modification with benzothiophene (BT) based acceptors. Density functional theory (DFT) and time-dependent DFT (TD-DFT) methods were employed at M06/6-311G (d, p) level to explore the geometrical, electronic, optical and photovoltaic properties of the designed derivatives. Lower energy gaps (E gap= 2.130–2.250 eV) and higher absorption wavelengths (λ max = 731.249-775.672 nm in chloroform solvent) were obtained for these chromophores. Least values of binding energy (E b= 0.528–0.554 eV) showed significantly high rate of exciton dissociation which indicated more charge transfer in BDTR and BDTD1-BDTD7. Further, the transition density matrix (TDM), hole-electron and density of states (DOS) graphs also supported the significant charge transfer within titled chromophores. Among all candidates, BDTD5 revealed the best results i.e., least energy gap (2.130 eV) and the bathochromic absorption spectra (775.672 nm). The open-circuit voltage (V oc) was calculated through Scharber’s equation by utilizing PTB7-Th donor. All derivatives showed comparable values of V oc with the reference chromophore (BDTR). Thus, it can be concluded that structural modification through the incorporation of BT acceptors is an effective approach for enhancing the optoelectronic and photovoltaic characteristics of the organic compounds.
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spelling doaj-art-7f62b43d932e489dab9d3a55423d6f5c2025-08-20T03:43:21ZengNature PortfolioScientific Reports2045-23222025-07-0115111810.1038/s41598-025-11718-zTuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiencyMashal Khan0Maria Zafar1Zafar Ullah2Iqra Shafiq3Saifullah Bullo4Tansir Ahamad5Ke Chen6Institute of Chemistry, Khwaja Fareed University of Engineering & Information TechnologyInstitute of Chemistry, Khwaja Fareed University of Engineering & Information TechnologyInstitute of Chemistry, Khwaja Fareed University of Engineering & Information TechnologyInstitute of Chemistry, Khwaja Fareed University of Engineering & Information TechnologyDepartment of Human and Rehabilitation Sciences, Begum Nusrat Bhutto Women UniversityDepartment of Chemistry, College of Science, King Saud UniversityDepartment of Infectious Diseases, The Affiliated Hospital of Southwest Medical UniversityAbstract Non-fullerene acceptors (NFAs) play a crucial role in enhancing the performance of bulk heterojunction organic solar cells (BHJ-OSCs). Therefore, new A–π–D–π–A configured NFAs (BDTD1-BDTD7) were developed from BDTR reference through terminal modification with benzothiophene (BT) based acceptors. Density functional theory (DFT) and time-dependent DFT (TD-DFT) methods were employed at M06/6-311G (d, p) level to explore the geometrical, electronic, optical and photovoltaic properties of the designed derivatives. Lower energy gaps (E gap= 2.130–2.250 eV) and higher absorption wavelengths (λ max = 731.249-775.672 nm in chloroform solvent) were obtained for these chromophores. Least values of binding energy (E b= 0.528–0.554 eV) showed significantly high rate of exciton dissociation which indicated more charge transfer in BDTR and BDTD1-BDTD7. Further, the transition density matrix (TDM), hole-electron and density of states (DOS) graphs also supported the significant charge transfer within titled chromophores. Among all candidates, BDTD5 revealed the best results i.e., least energy gap (2.130 eV) and the bathochromic absorption spectra (775.672 nm). The open-circuit voltage (V oc) was calculated through Scharber’s equation by utilizing PTB7-Th donor. All derivatives showed comparable values of V oc with the reference chromophore (BDTR). Thus, it can be concluded that structural modification through the incorporation of BT acceptors is an effective approach for enhancing the optoelectronic and photovoltaic characteristics of the organic compounds.https://doi.org/10.1038/s41598-025-11718-zNon-fullerene acceptorsPhotovoltaic responseBenzothiophene acceptorsDFTA–π–D–π–AFMOs
spellingShingle Mashal Khan
Maria Zafar
Zafar Ullah
Iqra Shafiq
Saifullah Bullo
Tansir Ahamad
Ke Chen
Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
Scientific Reports
Non-fullerene acceptors
Photovoltaic response
Benzothiophene acceptors
DFT
A–π–D–π–A
FMOs
title Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
title_full Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
title_fullStr Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
title_full_unstemmed Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
title_short Tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
title_sort tuning peripheral acceptors in pyran core functional materials to boost photovoltaic efficiency
topic Non-fullerene acceptors
Photovoltaic response
Benzothiophene acceptors
DFT
A–π–D–π–A
FMOs
url https://doi.org/10.1038/s41598-025-11718-z
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