ABSTRACT
Organic photovoltaics are a sustainable and cost-effective power-generation technology that may aid the move to zero-emission buildings, carbon neutral cities, and electric vehicles. While state-of-the-art organic photovoltaic devices can be encapsulated to withstand air and moisture, they are currently still susceptible to light-induced degradation, leading to a decline in the long-term efficiency of the devices. In this study, the role of ultraviolet (UV) radiation on a multilayer organic photovoltaic device is systematically uncovered using spectral filtering. By applying long-pass filters to remove different parts of the UV portion of the AM1.5G spectrum, two main photodegradation processes are shown to occur in the organic photovoltaic devices. A UV-activated process is found to cause a significant decrease in the photocurrent across the whole spectrum and is most likely linked to the deterioration of the charge extraction layers. In addition, a photodegradation process caused by UV-filtered sunlight is found to change the micromorphology of the bulk heterojunction material, leading to a reduction in photocurrent at high photon energies. These findings strongly suggest that the fabrication of inherently photostable organic photovoltaic devices will require the replacement of fullerene-based electron transporter materials with alternative organic semiconductors.
ABSTRACT
The technology behind a large area array of flexible solar cells with a unique design and semitransparent blue appearance is presented. These modules are implemented in a solar tree installation at the German pavilion in the EXPO2015 in Milan/IT. The modules show power conversion efficiencies of 4.5% and are produced exclusively using standard printing techniques for large-scale production.
ABSTRACT
The impact of side-chain variations on the photothermal stability of solar cells containing poly(benzodithiophene-diketopyrrolopyrrole) polymers are investigated in the absence of oxygen. Four different side-chains of benzodithiophene (BDT) are synthesized and copolymerized with diketopyrrolopyrrole (DPP) by Stille polymerization. The photothermal stability is measured as active layer blends with phenyl-C61-butyric acid methyl ester (PCBM) in encapsulated inverted photovoltaic cell architecture with zinc oxide and PEDOT: PSS as transport layers (ITO/ZnO/active layer/ PEDOT: PSS/Ag). Device degradation is correlated to the morphological behavior of the polymer:blend upon AM1.5 illumination (UV-visible light, 50 °C) and have been investigated by AFM, XRD, and UV-Vis. Once exposed to the light and to the temperature the BHJ stability is governed by two processes (i) PCBM crystallization and (ii) PCBM dimerization. Dimerization results in a rapid initial performance decrease followed by a more gradual decrease caused by a slower thermally activated crystallization. Depending on the blend morphology, dictated by the polymer's alkyl chain, the two processes occur to different extents thereby modulating the BHJ stability. Thus, of the polymer side-chains explored, linear alkyl side-chains stabilized the bulk heterojunction most effectively followed by no side-chain, alkoxy and branched side-chains. Lowering the concentration of fullerene in the active layer also reduces the rate of degradation across the polymers tested. This is a result of both the rate of crystallization and dimerization of fullerene being dependent on its concentration and the nature of the polymer side-chains. This approach appears to be a general strategy to increase the polymer:PCBM stability.
