Please use this identifier to cite or link to this item: https://ktisis.cut.ac.cy/handle/10488/18258
Title: Correlating Emissive Non‐Geminate Charge Recombination with Photocurrent Generation Efficiency in Polymer/Perylene Diimide Organic Photovoltaic Blend Films
Authors: Keivanidis, Panagiotis E. 
Kamm, Valentin 
Zhang, Weimin 
Floudas, George A. 
Laquai, Frédéric 
McCulloch, Iain 
Bradley, Donal D.C. 
Nelson, Jenny 
Major Field of Science: Engineering and Technology
Field Category: Electrical Engineering - Electronic Engineering - Information Engineering
Keywords: Luminescence;Microstructures;Non-geminate recombination;Organic photovoltaics (OPVs);Perylene diimides;Transport
Issue Date: 15-Mar-2012
Source: Advanced Functional Materials, 2012, vol. 22, no.11, pp. 2318-2326
Volume: 22
Issue: 11
Start page: 2318
End page: 2326
Journal: Advanced Functional Materials 
Abstract: Evidence for a correlation between the dynamics of emissive non-geminate charge recombination within organic photovoltaic (OPV) blend films and the photocurrent generation efficiency of the corresponding blend-based solar cells is presented. Two model OPV systems that consist of binary blends of electron acceptor N'-bis(1-ethylpropyl)-3,4,9,10-perylene tetracarboxy diimide (PDI) with either poly(9,9-dioctylfluorene-co-benzothiadiazole) (F8BT) or poly(9,9-dioctylindenofluorene-co-benzothiadiazole) (PIF8BT) as electron donor are studied. For the F8BT:PDI and PIF8BT:PDI devices photocurrent generation efficiency is shown to be related to the PDI crystallinity. In contrast to the F8BT:PDI system, thermal annealing of the PIF8BT:PDI layer at 90 °C has a positive impact on the photocurrent generation efficiency and yields a corresponding increase in PL quenching. The devices of both blends have a strongly reduced photocurrent on higher temperature annealing at 120 °C. Delayed luminescence spectroscopy suggests that the improved efficiency of photocurrent generation for the 90 °C annealed PIF8BT:PDI layer is a result of optimized transport of the photogenerated charge-carriers as well as of enhanced PL quenching due to the maintenance of optimized polymer/PDI interfaces. The studies propose that charge transport in the blend films can be indirectly monitored from the recombination dynamics of free carriers that cause the delayed luminescence. For the F8BT:PDI and PIF8BT:PDI blend films these dynamics are best described by a power-law decay function and are found to be temperature dependent.
ISSN: 1616-301X
DOI: 10.1002/adfm.201102871
Rights: © 2012 WILEY
Type: Article
Affiliation : Imperial College 
Max Planck Institute for Polymer Research 
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