Abstract
We report a series of semi-crystalline, low band gap (LBG) polymers and demonstrate the fabrication of highly efficient polymer solar cells (PSCs) in a thick single-cell architecture. The devices achieve a power conversion efficiency (PCE) of over 7% without any post-treatment (annealing, solvent additive, etc.) and outstanding long-term thermal stability for 200 h at 130 °C. These excellent characteristics are closely related to the molecular structures where intra- and/or intermolecular noncovalent hydrogen bonds and dipole-dipole interactions assure strong interchain interactions without losing solution processability. The semi-crystalline polymers form a well-distributed nano-fibrillar networked morphology with PC70BM with balanced hole and electron mobilities (a h/e mobility ratio of 1-2) and tight interchain packing (a π-π stacking distance of 3.57-3.59 Å) in the blend films. Furthermore, the device optimization with a processing additive and methanol treatment improves efficiencies up to 9.39% in a ∼300 nm thick conventional single-cell device structure. The thick active layer in the PPDT2FBT:PC 70BM device attenuates incident light almost completely without damage in the fill factor (0.71-0.73), showing a high short-circuit current density of 15.7-16.3 mA cm-2. Notably, PPDT2FBT showed negligible changes in the carrier mobility even at ∼1 μm film thickness. This journal is
Original language | English |
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Pages (from-to) | 3040-3051 |
Number of pages | 12 |
Journal | Energy and Environmental Science |
Volume | 7 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2014 Sept |
Externally published | Yes |
ASJC Scopus subject areas
- Environmental Chemistry
- Renewable Energy, Sustainability and the Environment
- Nuclear Energy and Engineering
- Pollution