| Literature DB >> 32233417 |
Lijiao Ma1,2, Shaoqing Zhang3, Huifeng Yao1, Ye Xu1,2, Jingwen Wang1,2, Yunfei Zu1,2, Jianhui Hou1,2.
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.Entities:
Keywords: charge carrier mobilities; high efficiency; non-fullerene organic solar cells; trap-state density; ultra-thick active layers
Year: 2020 PMID: 32233417 DOI: 10.1021/acsami.0c05172
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229