Efficient Diketopyrrolopyrrole-Based Small-Molecule Bulk-Heterojunction Solar Cells with Different Electron-Donating End-Groups
- Authors
- Kim, Yu Jin; Back, Jang Yeol; Kim, Seul-Ong; Jeon, Chan-Woo; Park, Chan Eon; Kim, Yun-Hi
- Issue Date
- Sep-2014
- Publisher
- Wiley - V C H Verlag GmbbH & Co.
- Keywords
- absorption; alkynes; conjugation; cross-coupling; solar cells
- Citation
- Chemistry - An Asian Journal, v.9, no.9, pp 2505 - 2513
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Chemistry - An Asian Journal
- Volume
- 9
- Number
- 9
- Start Page
- 2505
- End Page
- 2513
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/18818
- DOI
- 10.1002/asia.201402223
- ISSN
- 1861-4728
1861-471X
- Abstract
- A series of small molecules that contained identical pi-spacers (ethyne), a central diketopyrrolopyrrole (DPP) unit, and different aromatic electron-donating end-groups were synthesized and used in organic solar cells (OSCs) to study the effect of electron-donating groups on the device performance. The three compounds, DPP-A-Ph, DPP-A-Na, and DPP-A-An, possessed intense absorption bands that covered a wide range, from 350 to 750 nm, and relatively low HOMO energy levels, from -5.50 to -5.55 eV. DPP-A-An, which contained anthracene end-groups, demonstrated a stronger absorbance and a higher hole mobility than DPP-A-Ph, which contained phenyl groups, and DPP-A-Na, which contained naphthalene units. The power-conversion efficiencies (PCEs) of OSCs based on organic: PC71BM blends (1: 1, w/w) with a processed DIO additive were 3.93% for DPP-A-An, 3.02% for DPP-Na, and 2.26% for DPP-A-Ph. These findings suggest that a DPP core that is functionalized with electron-donating capping groups constitutes a promising new class of solution-processable small molecules for OSC applications.
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