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Ultrafast hole transfer mediated by polaron pairs in all-polymer photovoltaic blends

The charge separation yield at a bulk heterojunction sets the upper efficiency limit of an organic solar cell. Ultrafast charge transfer processes in polymer/fullerene blends have been intensively studied but much less is known about these processes in all-polymer systems. Here, we show that interfa...

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Detalles Bibliográficos
Autores principales: Wang, Rui, Yao, Yao, Zhang, Chunfeng, Zhang, Yindong, Bin, Haijun, Xue, Lingwei, Zhang, Zhi-Guo, Xie, Xiaoyu, Ma, Haibo, Wang, Xiaoyong, Li, Yongfang, Xiao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344565/
https://www.ncbi.nlm.nih.gov/pubmed/30674887
http://dx.doi.org/10.1038/s41467-019-08361-4
Descripción
Sumario:The charge separation yield at a bulk heterojunction sets the upper efficiency limit of an organic solar cell. Ultrafast charge transfer processes in polymer/fullerene blends have been intensively studied but much less is known about these processes in all-polymer systems. Here, we show that interfacial charge separation can occur through a polaron pair-derived hole transfer process in all-polymer photovoltaic blends, which is a fundamentally different mechanism compared to the exciton-dominated pathway in the polymer/fullerene blends. By utilizing ultrafast optical measurements, we have clearly identified an ultrafast hole transfer process with a lifetime of about 3 ps mediated by photo-excited polaron pairs which has a markedly high quantum efficiency of about 97%. Spectroscopic data show that excitons act as spectators during the efficient hole transfer process. Our findings suggest an alternative route to improve the efficiency of all-polymer solar devices by manipulating polaron pairs.