Morphological and physicochemical properties of dip-coated poly {(2,5-diyl pyrrole) [4-nitrobenzylidène]} (PPNB) thin films: towards photovoltaic applications

A new material: conjugated poly {(2,5-diyl pyrrole) [4-nitrobenzylidène]}, that we called (PPNB), has been synthesized and characterized. The cyclic voltammetry has been used in order to estimate first oxidation (Ep) and reduction (En) potentials of our polymer. These values have been assigned, respectively, to the position of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) and determination of the energy band gap which have been estimated to be 6.16, 3.89 and 2.27 eV respectively. Energy levels values of the HOMO and LUMO of the PPNB polymeric donor material were evaluated and the results are compatible with an electron transfer to C60 within an eventual junction, such values show that PPNB could be probed for applications in organic solar cells as donor material. PPNB Thin films have been deposited by dip-coating technique from Dichloromethane solvent with different polymer concentrations, and a dipping speed of 3.0 cm/min. For morphological characterization of the films scanning electron microscopy (SEM) was carried out. The samples, when observed by SEM, reveals that the films deposited are less dense, uniform. Cross-sectional SEM micrographs PPNB films show that thickness of the layers is homogeneous and has value of 35–40 nm. Optical characteristics of the polymer thin films were studied using UV-vis spectroscopy; absorption of wide range of wavelengths from 350 to 700 nm was observed. The optical band gap energy ranges between 1.9 eV and 1.94 eV. Based on these analyzes we realized heterojunction organic solar cells with the structure: ITO/Au/PPNB/C60/BCP/Al, the cells had a photovoltaique effect after J-V measuring, however the efficiency of photo generation under AM1.5 illumination was weak (about 0.02%) and needs to be improved

Cu-Ag bi-layer films in dielectric/metal/dielectric transparent electrodes as ITO free electrode in organic photovoltaic devices

Among ITO alternative, dielectric/metal/dielectric multilayer structures are one of the most often studied possible substituent. However, if their optical and electrical properties are systematically investigated it is not the same with regard to their mechanical properties. In the present manuscript we have studied the properties of ZnS/Cu/Ag/ZnS, ZnS/Cu/Ag/MO3 (with M ¼ Mo or W) structures. With a maximum transmission of 90% and a sheet resistance of 5 U/sq the optimum structure exhibits a figure of merit of 82 10-3 Ω-1 when l = 600 nm. Beyond these standard measures we proceeded to the study of the mechanical properties of the multilayer structures. The inner and outer bending tests show that the ZnS/ Cu/Ag/ZnS (or MO3) structures are more flexible than ITO, while their responses to scotch tests show that they exhibit a large adhesion to the substrate, glass or plastic. The scratching adhesion test puts in evidence that the adhesion to the substrate of the Ag layer is smaller than that of ZnS/Cu/Ag/ZnS, which is smaller than that of ITO. On the other hand, this test shows that the ZnS/Cu/Ag/ZnS (no cracks for L = 25 N) is less brittle than ITO (cracks L = 15N). Finally, when used as anode in organic solar cells, the structure ZnS/Cu/Ag/WO3 allows achieving the best efficiency, similar to that obtained with ITO

Dielectric/metal/dielectric alternative transparent electrode: observations on stability/degradation

The use of indium-free transparent conductive electrodes is of great interest for organic optoelectronic devices. Among the possible replacements for ITO, dielectric/metal/dielectric (D/M/D) multilayer structures have already proven to be quite efficient. One issue with organic devices is their lifetime, which depends not only on the organic molecules used but also on the electrodes. Therefore we study the variation, with elapsed time, of the electrical and optical properties of different D/M/D structures, with M  =  Ag or Cu/Ag. Six years after realization, it has been shown that if some structures retained an acceptable conductivity, some others became non-conductive. For a sample which remains conductive, in the case of a PET/MoO3/Ag/MoO3 multilayer structure, the sheet resistance changes from 5 Ω/sq–17 Ω/sq after six years. This evolution can be compared to that of a PET/ITO electrode that varies from 25 Ω/sq–900 Ω/sq after six years. It means that not only are the PET/MoO3/Ag/MoO3 multilayer structures more flexible than PET/ITO, but they can also be more stable. Nevertheless, if some PET/MoO3/Ag/MoO3 multilayer structures are quite stable, some others are not. This possible degradation appears to be caused primarily by the physical agglomeration of Ag, which can result in Ag film disruption. This Ag diffusion seems to be caused by humidity-induced degradation in these Ag-based D/M/D structures. Initially, defects begin to grow at a \u27nucleus\u27, usually a microscopic particle (or pinhole, etc), and then they spread radially outward to form a nearly circular pattern. For a critical density of such defects, the structure becomes non-conductive. Moreover the effect of humidity promotes Ag electrochemical reactions that produce Ag+ ions and enhances surface diffusivity with AgCl formation

On the exciton blocking layer at the interface organic/cathode in planar multiheterojunction organic solar cells

A successful approach to improve organic solar cell (OSC) performance is the introduction of a thin layer called exciton blocking layer (EBL) at the interface organic material/cathode. It is shown that, the EBL allows improving significantly the solar cells performances whatever the molecule used, either the well known bathocuproine (BCP) or the new molecule Z, 5[4-Me-3-N (2-OMe Phenyl)D4 thiazolidene], 2-thioxo-3-N(2-OEthylphenyl)thizolidine-4-one (ROETOM). The optimum thickness of the EBL in the case of ROETOM is 6 nm, while it is 9 nm in the case of BCP. These different behaviours are justified by the very high homogeneity of the ROETOM layer. Homogeneity which prevents easily metal atom diffusion when it is introduced in OSC and therefore 6 nm are sufficient to prevent metal atom diffusion into the acceptor

Broadening of the transmission range of dielectric/metal multilayer structures by using different metals

ZnS/M12/ZnS structures, with M12 ¼ Ag, Cu or Cu/Ag, were deposited under vacuum by simple joule heating effect (sublimation or evaporation). The optimum thicknesses of the different layers were experimentally determined: 50/45 nm for ZnS, 11 nm for Ag, 16 nm for Cu and 3 nm/9 nm for Cu/Ag. The presence of the double metal Cu/Ag interlayer induces a significant broadening of the optical transmittance spectrum of these structures. The properties of the structures depend strongly on deposition rate of the different films. When the deposition rates of ZnS, Cu are 0.15 nm/s and 0.30 nm/s for Ag, the averaged transmission, between 400 nm and 1000 nm is 85% while the sheet resistance is 5.0 ± 0.2 Ω/sq. These performances allow achieving an averaged factor of merit ΦM, between 400 nm and 700 nm, of 70 x 10-3 Ω-1. This averaged value tends toward those usually achieved by transparent conductive oxides

Optimum compromise between optical absorption and electrical property of the planar multi-heterojunction organic solar cells based with new thiazol derivative, the (2-thioxo-3-n-(2-methoxyphenyl) thiazolidin-4-one), as electron donor

International audienceThe synthesis of a new thiazol derivative, the (2-thioxo-3-N-(2-methoxyphenyl) thiazolidin-4-one) (called TH-2) is described. After characterization of the TH-2, the cyclic voltammetry study coupled with optical absorbance measurements show that its LUMO and HOMO are −3.5 and −5.5 respectively. Then the TH-2 is used as electron donor (ED) in organic solar cells (OSCs). The anode buffer layer being CuI the devices are based on the planar heterojunction TH-2/fullerene. Homogeneous amorphous films of TH-2 are obtained when it is deposited onto CuI. For an optimum TH-2 thickness of 20 nm, a power conversion efficiency of 0.42% is obtained. Then, in order to broaden the absorption range of the OSCs, it is coupled with the tetraphenyl-dibenzoperiflanthene, whose band structure matches the band structure of TH-2. Such new multilayer structure allows achieving a power conversion efficiency of 0.49%.</p

Optical and electronic proprieties of thin films based on (Z)-5-(4-chlorobenzylidene)-3-(2-ethoxyphenyl)-2 thioxothiazolidin-4-one, (CBBTZ) and possible application as exciton-blocking layer in heterojunction organic solar cells

In this work, organic thin film solar cells with structures based on CuPc/C60 bulk heterojunctions, have been fabricated and characterized. The effect of introducing an exciton blocking layer (EBL) between the active layer and the metal layer in the solar cell was investigated. For that (Z)-5-(4-chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one, that we called (CBBTZ) has been synthesized, characterized and probed as EBL. It was shown that optimized structures containing EBLs resulted in an improvement in solar cell conversion efficiencies. The energy levels corresponding to the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of the CBBTZ have been determined from the first oxidation and reduction potential respectively, using cyclic voltametric (CV) measurements. From CV curves, CBBTZ in dichloromethane showed a one electron reversible reduction and oxidation waves. The values of its HOMO and LUMO have been estimated to be 6.42 eV and 3.42 eV respectively. Such values show that CBBTZ could be probed as EBL in organic solar cells based on the ED/EA couple copper phthalocyanine(CuPc)/fullerene (C60). The photovoltaic solar cells have been obtained by sequential deposition under vacuum of the different films where their thicknesses were measured in situ by a quartz monitor. When obtained, the averaged efficiency of the cells using the CBBTZ is higher than that achieved without EBL layer

Optical and electronic proprieties of thin films based on (Z)-5-(4-chlorobenzylidene)-3-(2-ethoxyphenyl)-2 thioxothiazolidin-4-one, (CBBTZ) and possible application as exciton-blocking layer in heterojunction organic solar cells

In this work, organic thin film solar cells with structures based on CuPc/C60 bulk heterojunctions, have been fabricated and characterized. The effect of introducing an exciton blocking layer (EBL) between the active layer and the metal layer in the solar cell was investigated. For that (Z)-5-(4-chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one, that we called (CBBTZ) has been synthesized, characterized and probed as EBL. It was shown that optimized structures containing EBLs resulted in an improvement in solar cell conversion efficiencies. The energy levels corresponding to the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of the CBBTZ have been determined from the first oxidation and reduction potential respectively, using cyclic voltametric (CV) measurements. From CV curves, CBBTZ in dichloromethane showed a one electron reversible reduction and oxidation waves. The values of its HOMO and LUMO have been estimated to be 6.42 eV and 3.42 eV respectively. Such values show that CBBTZ could be probed as EBL in organic solar cells based on the ED/EA couple copper phthalocyanine(CuPc)/fullerene (C60). The photovoltaic solar cells have been obtained by sequential deposition under vacuum of the different films where their thicknesses were measured in situ by a quartz monitor. When obtained, the averaged efficiency of the cells using the CBBTZ is higher than that achieved without EBL layer

New dielectric/metal/dielectric electrode for organic photovoltaic cells using Cu:Al alloy as metal

International audienc