Effect of a high boiling point additive on the morphology of solution-processed P3HT-fullerene blends
Abstract
The use of high boiling point additives in solution processing has been widely employed to control the active layer morphology in bulk heterojunction organic solar cells. The morphology of the heterojunction is crucial in controlling charge separation and extraction by the electrodes, and therefore the power conversion efficiency (PCE) of the device. This paper presents a study of time-resolved fluorescence quenching in blends of P3HT containing varying concentrations of the fullerenes PC61BM or PC71BM. The relationship between the fluorescence quenching rate and fullerene concentration indicates that the fullerene molecules are dispersed within the P3HT film for up to 5% by mass of fullerene. For higher fullerene concentrations, the additional fullerene molecules aggregate and form fullerene domains. The high degree of phase segregation observed in these blends is beneficial for solar cell performance because the segregated fullerene phase provides electron percolation pathways through the blend. The addition of 1,8-diiodooctane (DIO) to the solutions for spin coating into films changes the scale of fullerene segregation when the ratio by mass of fullerene exceeds 20%. At high fullerene concentrations the rate of fluorescence quenching decreases in P3HT:PC61BM blends when prepared with DIO indicating a larger scale phase separation. The effect of DIO on the morphology of P3HT:PC71BM blends is the opposite in that it causes faster quenching in the blends. Overall the results show that DIO can be used to control the morphology of photovoltaic blends of P3HT with fullerenes.
Citation
Long , Y , Ward , A J , Ruseckas , A & Samuel , I D W 2016 , ' Effect of a high boiling point additive on the morphology of solution-processed P3HT-fullerene blends ' , Synthetic Metals , vol. 216 , pp. 23-30 . https://doi.org/10.1016/j.synthmet.2015.12.004
Publication
Synthetic Metals
Status
Peer reviewed
ISSN
0379-6779Type
Journal article
Rights
© 2015 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Description
Funding: UK Engineering and Physical Sciences Research Council (EPSRC) EP/L505079/1, EP/G03673X/1, EP/J009016/1Collections
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