Nonhalogenated polymers have great potential in the commercialization of organic photovoltaic (OPV) cells due to their advantage in low-cost preparation. However, non-halogenated polymers usually have high highest occupied molecular orbital (HOMO) energy levels and inferior self-aggregation properties in solution, thus resulting in low power conversion efficiencies (PCEs). Herein, two nonhalogenated polymers, PB1 and PB2, are prepared. When the polymers are used to fabricate OPV cells with BTP-eC9, the PB1-based device only gives a PCE of 5.3%, while the PB2-based device shows an outstanding PCE of 17.7%. After the introduction of PBDB-TF as the third component, the PB2:PBDB-TF:BTP-eC9-based device with an optimal weight ratio of 0.5:0.5:1 achieves a PCE up to 18.4%. More importantly, PB2 exhibits good compatibility with various nonfullerene acceptors to achieve better PCEs than those of classical polymer (PBDB-T and PBDB-TF)-based devices. When PB2 is combined with a wide-bandgap electron acceptor (F-BTA3), this device shows excellent PCE of 27.1% and 24.6% for 1 and 10 cm devices, respectively, under light intensity of 1000 lux light-emitting diode illumination. These results provide new insight in the rational design of novel nonhalogenated polymer donors for further development of low-cost materials and broadening the application of OPV cells.
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http://dx.doi.org/10.1002/adma.202105803 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
State Key Laboratory of Polymer Physics and Chemistry, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Medium-wide-bandgap (MWBG) organic photovoltaic (OPV) cells have emerged as a promising category with distinctive application possibilities, especially in environments characterized by specific light conditions, such as indoor spaces. However, there are few high-efficiency MWBG acceptors, and most of them are constructed through high-cost fused central units, which limits the industrialization of MWBG OPV cells. Here, two completely nonfused MWBG acceptors, TBT-38 and TBT-43 with different alkoxy substituent positions on the thiophene rings, are synthesized.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Zhejiang University, Hangzhou, Zhejiang 310027, China.
PSS is one of the best hole transport materials in organic photovoltaics (OPV). However, due to poor wettability, the aqueous PEDOT:PSS (a-PEDOT) is not applicable for inverted structured OPV as a hole transport layer (HTL) on top of the active layer. In this work, organic solvent-based PEDOT:PSS (o-PEDOT) with improved wettability was prepared by the solvent-replacement method through centrifugal ultrafiltration, dialysis membrane, and thermal evaporation.
View Article and Find Full Text PDFAdv Mater
December 2024
Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Designing donor (D) and acceptor (A) structures and discovering promising D-A combinations can effectively improve organic photovoltaic (OPV) device performance. However, to obtain excellent power conversion efficiency (PCE), the trial-and-error structural design in the infinite chemical space is time-consuming and costly. Herein, a deep learning (DL)-assisted design framework for OPV materials is proposed.
View Article and Find Full Text PDFJACS Au
November 2024
School of Polymer Science and Engineering, Center for Optoelectronic Materials and Devices, The University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Thermal stress is a critical factor causing long-term instability in bulk heterojunction (BHJ) layers of organic photovoltaic (OPV) devices. This study provides direct insights into the thermal properties of Y6, PM6, and their binary blends by employing fast differential scanning calorimetry (flash DSC) to analyze their chain dynamics. The glass transition temperatures ( ) of Y6 and PM6 were measured, with Y6 exhibiting a of 175.
View Article and Find Full Text PDFSci Rep
November 2024
Department of Chemistry, The University of Sheffield, Dainton Building, Brook Hill, Sheffield, S3 7HF, UK.
Metal-organic framework nanosheets (MONs) have proved themselves to be useful additives for enhancing the performance of a variety of thin film solar cell devices. However, to date only isolated examples have been reported. In this work we take advantage of the modular structure of MONs in order to resolve the effect of their different structural and optoelectronic features on the performance of organic photovoltaic (OPV) devices.
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