Abstract

We present measurements of the outdoor stability of PCDTBT:PC71BM based bulk heterojunction organic solar cells for over the course of a year. We find that the devices undergo a burn-in process lasting 450 hours followed by a TS80 lifetime of up to 6200 hours. We conclude that in the most stable devices, the observed TS80 lifetime is limited by thermally-induced stress between the device layers, as well as materials degradation as a result of edge-ingress of water or moisture through the encapsulation.

Highlights

  • The past decade has witnessed a steady growth in the efficiency of organic photovoltaics (OPVs), with power conversion efficiencies (PCEs) currently exceeding 10%1–4; a value regarded as a significant step in the so-called 10/10 target for organic photovoltaics (10% efficiency and 10 years lifetime)

  • We find that when tested outdoors, PCDTBT:PC71BM devices undergo a burn-in stage characterized by an initial rapid loss in efficiency, followed by a period of slower, linear degradation - a result reported in laboratory testing[37]

  • Our study demonstrates that PCDTBT based OPVs have promising stability when tested under real-world conditions, this currently appears to be limited by the efficiency of our encapsulation materials and techniques with further refinements in testing protocols being required

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Summary

Results and Discussion

The devices explored in this work were based on an ITO/HTL/Active layer/Ca/Al heterostructure as shown in Fig. 1(b), with each device containing 6 pixels. It can be seen that all the devices undergo a burn-in process during which the Voc and FF degrade rapidly, with the Jsc undergoing a relatively smaller reduction Such phenomena have been observed when PCDTBT:PC71BM OPVs have been aged under laboratory conditions[34]. We find that in summer, the temperature inside the chamber can change at a rate of 10°C/hour, reaching a maximum temperature of 75°C; a process that we believe causes thermally induced stress between the different layers in the device resulting in additional path-ways for the diffusion of oxygen or moisture into the film This may point to a thermal or UV-assisted break-down of the encapsulation-epoxy which results in enhanced photo-oxidation of the active organic layer. Enhanced device stability under real-world operation is expected through the use of more sophisticated encapsulation techniques, together with the use of UV400 filtration

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