1,721,022 research outputs found
High figure-of-merit transparent copper–zinc oxide window electrodes for organic photovoltaics
No full textWe report a copper–zinc oxide bilayer electrode supported on flexible polyethylene terephthalate (PET) with a sheet resistance of 11. 3 Ω sq−1 and average transparency of 84.6% in the wavelength range of 400–800 nm. The copper film is perforated with a dense array of sub-micron diameter apertures fabricated using polymer-blend lithography, which imparts broad band anti-reflectivity. We demonstrate proof-of-principle that it is possible to fabricate the polymer mask by dip coating which is a scalable deposition method compatible with roll-to-roll processing. During storage of the electrode at ambient temperature the ZnO layer is spontaneously doped with copper from the underlying copper film and so the thin ZnO layer serves both as an anti-reflecting layer and an excellent electron transport layer. When compared with commercially available indium tin oxide coated (ITO) plastic substrates this electrode exhibits superior stability towards bending deformation, with no change in sheet resistance after bending through a 4 mm radius of curvature 100 times. Model inverted organic photovoltaic (OPV) devices using this electrode exhibit a champion power conversion efficiency of ~8.7%, which is the highest reported efficiency to date for an OPV device using a copper based transparent electrode, outperforming identical devices using ITO coated plastic as the transparent electrode
Copper substrate electrode for efficient top-illuminated organic photovoltaics
No full textIt is now recognized that for solution processed organic photovoltaics (OPVs) to be manufactured on a large scale the thickness of the photoactive layer must be substantially increased beyond the currently used ≤150 nm. We show that copper can replace silver as the reflective substrate electrode in high performance top-illuminated OPVs without compromising device power conversion efficiency when the photoactive layer is thick enough to absorb the majority of incident photons on first pass through the photo-active layer. Copper is one hundredth of the cost of Ag, enabling a significant reduction in the bill of materials for OPV manufacture
Copper light-catching electrodes for organic photovoltaics
No full textOptically thin copper films with a random array of sub-optical wavelength apertures couple strongly with light in the wavelength range 600–800 nm due to excitation of surface plasmonic resonances. Herein we show that this trapped light can be used to excite electronic transitions in a nearby strongly absorbing organic semiconductor before the plasmonic excitations dissipate their energy as heat into the metal. This energy transfer process is demonstrated using model small molecule and polymer photovoltaic devices (based on chloro-aluminium phthalocyanine:C60 and PCE-10:PC70BM heterojunctions respectively) in conjunction with a nano-hole copper electrode formed by thermal annealing an optically thin Cu film supported on polyethylene terephthalate. The efficiency of this process is shown to be highest for wavelengths in the range 650–750 nm, which is part of the solar spectrum that is weakly absorbed by today's high performance organic photovoltaic devices, and so these findings demonstrate that this type of electrode could prove useful as a low cost light catching element in high performance organic photovoltaics
Fabrication of copper window electrodes with ≈10<sup>8</sup> apertures cm<sup>−2</sup> for organic photovoltaics
No full textA powerful approach to increasing the far-field transparency of copper film window electrodes which simultaneously reduces intraband absorption losses for wavelengths <550 nm and suppresses reflective losses for wavelengths >550 nm is reported. The approach is based on incorporation of a random array of ≈100 million circular apertures per cm2 into an optically thin copper film, with a mean aperture diameter of ≈500 nm. A method for the fabrication of these electrodes is described that exploits a binary polymer blend mask that self-organizes at room temperature from a single solution, and so is simple to implement. Additionally all of the materials used in electrode fabrication are low cost, low toxicity, and widely available. It is shown that these nanostructured copper electrodes offer an average far-field transparency of ≥80% and sheet resistance of ≤10 Ω sq−1 when used in conjunction with a conventional solution processed ZnO electron transport layer and their utility in inverted organic photovoltaic devices is demonstrated
Retarding oxidation of copper nanoparticles without electrical isolation and the size dependence of work function
No full textCopper nanoparticles (CuNPs) are attractive as a low-cost alternative to their gold and silver analogues for numerous applications, although their potential has hardly been explored due to their higher susceptibility to oxidation in air. Here we show the unexpected findings of an investigation into the correlation between the air-stability of CuNPs and the structure of the thiolate capping ligand; of the eight different ligands screened, those with the shortest alkyl chain, –(CH2)2–, and a hydrophilic carboxylic acid end group are found to be the most effective at retarding oxidation in air. We also show that CuNPs are not etched by thiol solutions as previously reported, and address the important fundamental question of how the work function of small supported metal particles scales with particle size. Together these findings set the stage for greater utility of CuNPs for emerging electronic applications
Assessing the suitability of copper thiocyanate as a hole-transport layer in inverted CsSnI3 perovskite photovoltaics
No full textWe report the findings of a study into the suitability of copper (I) thiocyanate (CuSCN) as a hole-transport layer in inverted photovoltaic (PV) devices based on the black gamma phase (B-γ) of CsSnI3 perovskite. Remarkably, when B-γ-CsSnI3 perovskite is deposited from a dimethylformamide solution onto a 180–190 nm thick CuSCN film supported on an indium-tin oxide (ITO) electrode, the CuSCN layer is completely displaced leaving a perovskite layer with high uniformity and coverage of the underlying ITO electrode. This finding is confirmed by detailed analysis of the thickness and composition of the film that remains after perovskite deposition, together with photovoltaic device studies. The results of this study show that, whilst CuSCN has proved to be an excellent hole-extraction layer for high performance lead-perovskite and organic photovoltaics, it is unsuitable as a hole-transport layer in inverted B-γ-CsSnI3 perovskite photovoltaics processed from solution
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