化学
分子间力
光伏系统
载流子
能量转换效率
化学物理
光电子学
有机太阳能电池
超快激光光谱学
电场
接受者
吸收(声学)
电荷(物理)
瞬态(计算机编程)
电子迁移率
静电学
纳米技术
聚合物
分子
材料科学
物理化学
光学
电气工程
有机化学
物理
工程类
操作系统
激光器
量子力学
计算机科学
凝聚态物理
作者
Huifeng Yao,Yong Cui,Deping Qian,Carlito S. Ponseca,Alireza Honarfar,Ye Xu,Jingming Xin,Zhenyu Chen,Ling Hong,Bowei Gao,Runnan Yu,Yunfei Zu,Wei Ma,Pavel Chábera,Tönu Pullerits,Arkady Yartsev,Feng Gao,Jianhui Hou
摘要
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.
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