Source abstract
Abstract
The high-efficiency organic solar cells (OSCs) with thicker active layers are potential candidates for the fabrication of large-area solar panels. The low charge carrier mobility of the photoactive materials has been identified as the major problem hindering the photovoltaic performance of the thick-film OSCs. In this study, high performance of ultra-thick-film OSCs employing a nonfullerene acceptor BTP-4Cl and a polymer donor PBDB-TF is demonstrated. Two blends (PBDB-TF:BTP-4Cl and PBDB-TF:IT-4F) show comparable mobilities and excellent photovoltaic characteristics in thin-film devices, while in the 1000 nm thick devices, although they both exhibit desirable and balanced mobilities, the PBDB-TF:BTP-4Cl-based blend possesses lower trap-state density than the IT-4F-based counterpart, leading to lower trap-assist recombination, longer carrier lifetime, and thus a much higher short-circuit current density in the device. As a result, the BTP-4Cl-based 1000 nm thick OSC achieves a remarkable power conversion efficiency of 12.1%, which greatly outperforms the IT-4F-based devices (4.72%). Furthermore, for a 1000 nm thick device with an active area of 4 cm2, a promising efficiency of 10.1% was obtained, showing its great potential in future large-scale production.
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Affiliations
State Key Laboratory of Polymer Physics and Chemistry, Beijing National Laboratory for Molecular, Sciences CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P. R. China
University of Chinese Academy of Sciences, Beijing 100049, P. R. China
School of Chemistry and Biology Engineering, University of Science and Technology Beijing, Beijing 100083, P. R. China
Funding
National Natural Science Foundation of China · Chinese Academy of Sciences · Beijing National Laboratory for Molecular Sciences