Abstract
The charge carrier dynamics of a new polymer-fullerene blend are examined on the femtosecond to the millisecond time scale. The full time range is globally fitted using a chemical reaction rate model that includes all key processes, charge generation, energy transfer, charge separation, and recombination, over the full 12 orders of magnitude in time and a factor of 33 in light intensity. Particular attention is paid to the charge recombination processes and it is found that they are highly material specific. Comparison of the dynamics to those of a previously studied polymer:fullerene blend reveals that while for one blend the recombination dynamics are mainly controlled by geminate recombination, the charge recombination in the presently studied polymer:fullerene blend are entirely controlled by non-geminate electron-hole recombination. Carrier density dependence of the non-geminate recombination rate is analyzed and a correlated disorder model of site energies is proposed to explain the observed dependency. The dynamics of a new polymer-fullerene blend are globally fitted using a chemical reaction rate model over 12 orders of magnitude in time and a factor of 33 in light intensity. The charge recombination is non-geminate and a correlated disorder model of site energies is proposed to explain the observed dependency.
| Original language | English |
|---|---|
| Article number | 1301706 |
| Pages (from-to) | Art: 1301706 |
| Number of pages | 9 |
| Journal | Advanced Energy Materials |
| Volume | 4 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 3 Jun 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- nongeminate recombination
- organic solar cells
- recombination dynamics
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