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Unraveling the Solution Aggregation Structures and Processing Resiliency of High‐Efficiency Organic Photovoltaic Blends

Mengyuan GaoSchool of Materials Science & Engineering Tianjin Key Laboratory of Molecular Optoelectronic Sciences Key Laboratory of Organic Integrated Circuits Ministry of Education Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Tianjin University Tianjin 300350 ChinaChunlong SunSchool of Materials Science & Engineering Tianjin Key Laboratory of Molecular Optoelectronic Sciences Key Laboratory of Organic Integrated Circuits Ministry of Education Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Tianjin University Tianjin 300350 ChinaYiwen LiNational Facility for Protein Science Shanghai Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201210 ChinaNa LiNational Facility for Protein Science Shanghai Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201210 ChinaHanqiu JiangInstitute of High Energy Physics Chinese Academy of Sciences Beijing 100049 ChinaChunyong HeInstitute of High Energy Physics Chinese Academy of Sciences Beijing 100049 ChinaYu ChenInstitute of High Energy Physics Chinese Academy of Sciences Beijing 100049 ChinaWenchao ZhaoCo‐Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Materials Science and Engineering Nanjing Forestry University Nanjing 210037 ChinaJianhui HouState Key Laboratory of Polymer Physics and Chemistry, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences Beijing 100190 ChinaLong YeSchool of Materials Science & Engineering Tianjin Key Laboratory of Molecular Optoelectronic Sciences Key Laboratory of Organic Integrated Circuits Ministry of Education Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Tianjin University Tianjin 300350 China
2024en
ABI

Аннотация

Abstract The solution aggregation structure of conjugated polymers is crucial to the morphology and resultant optoelectronic properties of organic electronics and is of considerable interest in the field. Precise characterizations of the solution aggregation structures of organic photovoltaic (OPV) blends and their temperature‐dependent variations remain challenging. In this work, the temperature‐dependent solution aggregation structures of three representative high‐efficiency OPV blends using small‐angle X‐ray/neutron scattering are systematically probed. Three cases of solution processing resiliency are elucidated in state‐of‐the‐art OPV blends. The exceptional processing resiliency of high‐efficiency PBQx‐TF blends can be attributed to the minimal changes in the multiscale solution aggregation structure at elevated temperatures. Importantly, a new parameter, the percentage of acceptors distributed within polymer aggregates ( Ф ), for the first time in OPV blend solution, establishes a direct correlation between Ф and performance is quantified. The device performance is well correlated with the Kuhn length of the cylinder related to polymer aggregates L 1 at the small scale and the Ф at the large scale. Optimal device performance is achieved with L 1 at ≈30 nm and Ф within the range of 60 ± 5%. This study represents a significant advancement in the aggregation structure research of organic electronics.

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