Abstract
Ternary organic solar cells (OSCs) have attracted much research attention, as they can maintain the simplicity of the single-junction device architecture while broadening the absorption range of OSCs. However, one main challenge that limits the development of ternary OSCs is the difficulty in controlling the morphology of ternary OSCs. In this paper, an effective approach to control the morphology is presented that leads to multiple cases of efficient nonfullerene ternary OSCs with efficiencies of up to 11.2%. This approach is based on a donor polymer with strong temperature dependent aggregation properties processed from hot solutions without any solvent additives and a pair of small molecular acceptors (SMAs) that have similar surface tensions and thus low propensity to form discrete phases. Such a ternary blend exhibits a simplified bulk-heterojunction morphology that is similar to the morphology of previously reported binary blends. As a result, an almost linear relationship between VOC and film composition is observed for all nonfullerene ternary devices. Meanwhile, by carefully designing a control system with a large interfacial tension, a different phase separation and VOC dependence is demonstrated. This morphology control approach can be applicable to more material systems and accelerates the development of the ternary OSC field.
| Original language | English |
|---|---|
| Article number | 1701370 |
| Journal | Advanced Energy Materials |
| Volume | 8 |
| Issue number | 9 |
| DOIs | |
| State | Published - 26 Mar 2018 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 7 Affordable and Clean Energy
Keywords
- morphology
- non-fullerene
- organic solar cells
- photovoltaics
- small molecular acceptors
- surface tension
- ternary blends
Fingerprint
Dive into the research topics of 'Multiple Cases of Efficient Nonfullerene Ternary Organic Solar Cells Enabled by an Effective Morphology Control Method'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver