Dissociation of singlet excitons dominates photocurrent improvement in
high-efficiency non-fullerene organic solar cells
- Qicong Li,
- Shizhong Yue
, - Zhitao Huang,
- Chao Li,
- Jiaqian Sun,
- Keqian Dong,
- Zhijie Wang
, - Kong Liu,
- Shengchun Qu
Qicong Li
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileShizhong Yue

Institute of Semiconductors Chinese Academy of Sciences
Author ProfileZhitao Huang
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileChao Li
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileJiaqian Sun
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileKeqian Dong
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileZhijie Wang

Institute of Semiconductors Chinese Academy of Sciences
Corresponding Author:wangzj@semi.ac.cn
Author ProfileKong Liu
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileShengchun Qu
Institute of Semiconductors Chinese Academy of Sciences
Author ProfileAbstract
In organic solar cells, the singlet and triplet excitons dissociate into
free charge carriers with different mechanisms due to their opposite
spin state. Therefore, the ratio of the singlet and triplet excitons
directly affects the photocurrent. Many methods were used to optimize
the performance of the low-efficiency solar cell by improving the ratio
of triplet excitons, which shows a long diffusion length. Here we
observed that in high-efficiency systems, the proportion of singlet
excitons under linearly polarized light excitation is higher than that
of circularly polarized light. Since the singlet charge transfer state
has lower binding energy than the triplet state, it makes a significant
contribution to the charge carrier generation and enhancement of the
photocurrent. Further, the positive magnetic field effect reflects that
singlet excitons dissociation plays a major role in the photocurrent,
which is opposite to the case of low-efficiency devices where triplet
excitons dominate the photocurrent.