| Literature DB >> 31017418 |
Huifeng Yao1, Yong Cui1,2, Deping Qian3, Carlito S Ponseca3, Alireza Honarfar4, Ye Xu1,2, Jingming Xin5, Zhenyu Chen5, Ling Hong1,2, Bowei Gao1,2, Runnan Yu1,2, Yunfei Zu1,2, Wei Ma5, Pavel Chabera4, Tönu Pullerits4, Arkady Yartsev4, Feng Gao3, Jianhui Hou1,2.
Abstract
Although significant improvements have been achieved for organic photovoltaic cells (OPVs), the top-performing devices still show power conversion efficiencies far behind those of commercialized solar cells. One of the main reasons is the large driving force required for separating electron-hole pairs. Here, we demonstrate an efficiency of 14.7% in the single-junction OPV by using a new polymer donor PTO2 and a nonfullerene acceptor IT-4F. The device possesses an efficient charge generation at a low driving force. Ultrafast transient absorption measurements probe the formation of loosely bound charge pairs with extended lifetime that impedes the recombination of charge carriers in the blend. The theoretical studies reveal that the molecular electrostatic potential (ESP) between PTO2 and IT-4F is large, and the induced intermolecular electric field may assist the charge generation. The results suggest OPVs have the potential for further improvement by judicious modulation of ESP.Entities:
Year: 2019 PMID: 31017418 DOI: 10.1021/jacs.8b12937
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419