Functional substrates for flexible organic photovoltaic cells
Proceedings of SPIE - The International Society for Optical Engineering 5938 (2005) 1-9
Abstract:
Along with efficiency and lifetime, costs are one of the most important aspects for the commercialization of organic solar cells. Thinking of large scale production of organic solar cells by an efficient reel-to-reel process, the materials are expected to determine the costs of the final product. Our approach is to develop functional substrates for organic solar cells which have the potential for cost effective production. The functionality is obtained by combining periodically microstructured substrates with lamellar electrode structures. Such structured substrates were fabricated by cost effective replication from masterstructures that were generated by large area interference lithography. Two cell architectures were investigated - holographic microprisms and interdigital buried nanoelectrodes. A structure period of 20μm in combination with a 2μm wide metal grid was chosen for the microprism cells based on the results of electrical calculations. Current-voltage curves with reasonable fill factors were measured for these devices. A significant light trapping effect was predicted from optical simulations. Interdigital buried nanoelectrodes are embedded in the photoactive layer of the solar cell. Separated interdigital metal electrodes with a sufficiently high parallel resistance were manufactured despite a small electrode distance below 400 nm. Experimental results on first photovoltaic devices will be presented. We observe an insufficient rectification of the photovoltaic device which we attribute to partial electron injection into the gold anode.Organic solar cells using inverted layer sequence
Thin Solid Films 491:1-2 (2005) 298-300
Abstract:
We report on a concept for organic solar cells where the layer sequence is inverted compared to the conventional setup. In such a configuration a conducting polymer layer is used as the transparent anode which is able to transport the photocurrent laterally to a metal grid. For the anode a low sheet resistance and a work function matching approximately the chemical potential of the holes of the illuminated photoactive layer is required. We showed that the poly(3,4-ethylenedioxythiophene) doped with poly(styrenesulfonate) fits to these requirements. In our setup an aluminium cathode was used. It turned out that for the inverted setup the interface between aluminium and the photoactive layer has to be protected against oxidation. Our investigations show that with a thin layer (20 nm) of electron-beam deposited titanium between aluminium and the photoactive layer the electrical contact is drastically improved. A solar cell efficiency of (1.4 ± 0.3)% was reached in this case. © 2005 Elsevier B.V. All rights reserved.Azetidinium as Cation in Lead Mixed Halide Perovskite Nanocrystals of Optoelectronic Quality
Abstract:
Previous theoretical calculations show azetidinium has the right radial size to form a 3D perovskite with lead halides [1], and has been shown to impart, as the A-site cation of ABX3 unit, beneficial properties to ferroelectric perovskites [2]. However, there has been very limited research into its use as the cation in lead halide perovskites to date. In this communication we report the synthesis and characterization of azetidinium-based lead mixed halide perovskite colloidal nanocrystals. The mixed halide system is iodine and chlorine unlike other reported nanocrystals in the literature where the halide systems are either iodine/bromine or bromine/chlorine. UV-visible absorbance data, complemented with photoluminescence spectroscopy, reveals an indirect-bandgap of about 1.96 eV for our nanocrystals. Structural characterization using TEM shows two distinct interatomic distances (2.98 +/- 0.15 Angstroms and 3.43 +/- 0.16 Angstroms) and non-orthogonal lattice angles (approximately 112 degrees) intrinsic to the nanocrystals with a probable triclinic structure revealed by XRD. The presence of chlorine and iodine within the nanocrystals is confirmed by EDS spectroscopy. Finally, light-induced electron paramagnetic resonance (LEPR) spectroscopy with PCBM confirms the photoinduced charge transfer capabilities of the nanocrystals. The formation of such semiconducting lead mixed halide perovskite using azetidinium as the cation suggests a promising subclass of hybrid perovskites holding potential for optoelectronic applications such as in solar cells and photodetectors.In-situ observation of stacking fault evolution in vacuum-deposited C60
Applied Physics Letters AIP Publishing