14.7% Efficiency Organic Photovoltaic Cells Enabled by Active Materials with a Large Electrostatic Potential Difference

Huifeng Yao, Yong Cui, Deping Qian, Carlito S. Ponseca, Alireza Honarfar, Ye Xu, Jingming Xin, Zhenyu Chen, Ling Hong, Bowei Gao,

Journal of the American Chemical Society · 2019 · 518 citations · 39 references

Concepts

TL;DR

Organic photovoltaic cells still lag behind commercial solar cells in efficiency, largely because they require a large driving force to separate electron–hole pairs. Ultrafast transient absorption and theoretical studies reveal that a large electrostatic potential between PTO2 and IT‑4F creates an intermolecular electric field that stabilizes loosely bound charge pairs, extending their lifetime and aiding charge generation. The single‑junction OPV achieved a 14.7% power‑conversion efficiency with efficient charge generation at a low driving force, indicating that tuning the electrostatic potential can further enhance performance.

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.

References

39