Abstract
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (PDI):polymer solar cells can be circumvented when two simple rules are respected; the aggregate size of PDI remains short enough and the omnipresent PDI aggregates are electronically interconnected. Following these guidelines, a PCE of 3.7% is delivered by using the solution-processable, planar PDI monomer of N,N′-bis(1-ethylpropyl)-perylene-3,4,9,10- tetracarboxylic diimide as the electron acceptor mixed with the low-energy gap polymeric donor poly[(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b;4,5- b′]dithiophene)-2,6-diyl-alt-(4-(2-ethylhexanoyl)-thieno[3,4-b]thiophene)) -2,6-diyl] (PBDTTT-CT). The PBDTTT-CT:PDI composite absorbs strongly the light in the region of 400 nm-800 nm and after adding a small amount of 1,8-diiodooctane (DIO) efficient photocurrent generation is achieved. Space-charge limited dark current and transient photovoltage measurements suggest that the use of the DIO component optimizes the electron/hole carrier mobility ratio, suppresses the non-geminate recombination losses and improves the charge extraction efficiency.
| Original language | English |
|---|---|
| Pages (from-to) | 14348-14353 |
| Number of pages | 6 |
| Journal | Journal of Materials Chemistry A |
| Volume | 2 |
| Issue number | 35 |
| DOIs | |
| State | Published - 21 Sep 2014 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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