Abstract
A weak electron acceptor, 4,9-bis(5-bromothiophen-2-yl)-2-(2-ethylhexyl)- benzo[f]isoindole-1,3-dione (BIDO) was designed and synthesized. Polymer P1 derived from BIDO and 9,9-dioctylfluorene-2,7-diboronic acid bis(1,3-propanediol) ester by Suzuki cross-coupling reaction has a band gap of 2.41 eV. To expand the absorption range, a different amount of BIDO was copolymerized with a diketopyrrolopyrrole monomer to produce a series of copolymers Pa-c. The optical properties, electrochemical behavior, and energy levels of these four copolymers were investigated. The photovoltaic properties copolymers Pa-c were studied. A photovoltaic device containing Pc and [70]PCBM with a ratio of 1:2 had a power conversion efficiency of 1.17%.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 5543-5552 |
| Number of pages | 10 |
| Journal | Polymer |
| Volume | 54 |
| Issue number | 21 |
| DOIs | |
| State | Published - Oct 4 2013 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 7 Affordable and Clean Energy
Keywords
- Conjugated copolymer
- Donor-acceptor
- Organic solar cells
Fingerprint
Dive into the research topics of 'Synthesis and characterizations of conjugated copolymers containing benzo[f]isoindole-1,3-dione and diketopyrrolopyrrole units'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS