Critical light instability in CB/DIO processed PBDTTT-EFT: PC71BM organic photovoltaic devices

Organic photovoltaic (OPV) devices often undergo ‘burn-in’ during the early stages of operation, this period describing the relatively rapid drop in power output before stabilising. For normal and inverted PBDTTT-EFT:PC71BM OPVs prepared according to current protocols, we identify a critical and sev...

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Hauptverfasser: Pearson, Andrew (VerfasserIn) , Hopkinson, Paul E. (VerfasserIn) , Couderc, Elsa (VerfasserIn) , Domanski, Konrad (VerfasserIn) , Abdi-Jalebi, Mojtaba (VerfasserIn) , Greenham, Neil C. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 8 January 2016
In: Organic electronics
Year: 2016, Jahrgang: 30, Pages: 225-236
DOI:10.1016/j.orgel.2015.12.024
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.orgel.2015.12.024
Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S1566119915302445
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Verfasserangaben:Andrew J. Pearson, Paul E. Hopkinson, Elsa Couderc, Konrad Domanski, Mojtaba Abdi-Jalebi, Neil C. Greenham

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520 |a Organic photovoltaic (OPV) devices often undergo ‘burn-in’ during the early stages of operation, this period describing the relatively rapid drop in power output before stabilising. For normal and inverted PBDTTT-EFT:PC71BM OPVs prepared according to current protocols, we identify a critical and severe light-induced burn-in phase that reduces power conversion efficiency by at least 60% after 24 hours simulated AM1.5 illumination. Such losses result primarily from a reduction in photocurrent, and for inverted devices we correlate this process in-situ with the simultaneous emergence of space-chare effects on the μs timescale. The effects of burn in are also found to reduce the lifetime of photogenerated charge carriers, as determine by in-situ transient photovoltage measurements. To identify the underlying mechanisms of this instability, a range of techniques are employed ex-situ to separate bulk- and electrode-specific degradation processes. We find that whilst the active layer nanostructure and kinetics of free charge generation remain unchanged, partial photobleaching (6% of film O.D.) of PBDTTT-EFT:PC71BM occurs alongside an increase in the ground state bleach decay time of PBDTTT-EFT. We hypothesise that this latter observation may reflect relaxation from excited states on PBDTTT-EFT that do not undergo dissociation into free charges. Owing to the poor lifetime of the reference PBDTTT-EFT:PC71BM OPVs, the fabrication protocol is modified to identify routes for stability enhancement in this initially promising solar cell blend. 
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