Synthèse de nouveaux chromophores pour les cellules photovoltaïques

Date du colloque : 06/2011</p

New chromophores for organic solar cells

Date du colloque : 06/2011</p

Miniaturization of molecular conjugated systems for organic solar cells: towards pigmy donors

Organic solar cells with short-circuit current densities and conversion efficiencies of ca. 7.0 mA cm(-2) and 2.0%, respectively, have been fabricated with a very small molecular donor based on substituted triarylamines

MoO3/CuI hybrid buffer layer for the optimization of organic solar cells based on a donor-acceptor triphenylamine

We investigate the effect of anode buffer layers (ABLs) on the performances of multi-layer heterojunction solar cells with thienylenevinylene-triphenylamine with peripheral dicyanovinylene groups (TDCV-TPA) as donor material and fullerene C-60 as acceptor. The deposition of a CuI layer between the ITO anode and the electron donor significantly improves the short-circuit current density (J(sc)) and fill factor (FF) but reduces the open-circuit voltage (V-oc). On the other hand, a MoO3 buffer layer increases the V-oc but leads to limited J(sc) and FF values, thus reducing power conversion efficiency (PCE). In this context, we show that the use of a hybrid anode buffer layer MoO3/CuI leads to a considerable improvement of the cells performances and a PCE of 2.50% has been achieved. These results are discussed on the basis of the dual function of MoO3 and CuI. While both of them reduce the hole injection barrier, CuI improves the conductivity of the organic film through an improvement of molecular order while MoO3 prevents leakage current through the diode. Finally the results of a cursory study of the ageing process provide further support to this interpretation of the effects of the various buffer layers. (C) 2012 Elsevier B.V. All rights reserved

Tuning of the Photovoltaic Parameters of Molecular Donors by Covalent Bridging

The synthesis of donor-acceptor molecules involving triarylamines and dicyanovinyl blocks is described. Optical and electrochemical results show that rigidification of the acceptor part of the molecule by a covalent bridge leads to a ca. 0.20 eV increase of the band gap due to a parallel increase of the lowest unoccupied molecular orbital level. A preliminary evaluation of these compounds as donor materials in organic solar cells shows that although this structural modification reduces the light-harvesting properties of the donor molecule, it nevertheless induces an increase of the efficiency of the resulting solar cells due to a simultaneous improvement of the open-circuit voltage and fill factor

Modeling lightning-NOx chemistry on a sub-grid scale in a global chemical transport model

For the first time, a plume-in-grid approach is implemented in a chemical transport model (CTM) to parameterize the effects of the nonlinear reactions occurring within high concentrated NO_<i>x</i> plumes from lightning NO_<i>x</i> emissions (LNO_<i>x</i>) in the upper troposphere. It is characterized by a set of parameters including the plume lifetime, the effective reaction rate constant related to NO_<i>x</i>–O₃ chemical interactions, and the fractions of NO_<i>x</i> conversion into HNO₃ within the plume. Parameter estimates were made using the Dynamical Simple Model of Atmospheric Chemical Complexity (DSMACC) box model, simple plume dispersion simulations, and the 3-D Meso-NH (non-hydrostatic mesoscale atmospheric model). In order to assess the impact of the LNO_<i>x</i> plume approach on the NO_<i>x</i> and O₃ distributions on a large scale, simulations for the year 2006 were performed using the GEOS-Chem global model with a horizontal resolution of 2° × 2.5°. The implementation of the LNO_<i>x</i> parameterization implies an NO_<i>x</i> and O₃ decrease on a large scale over the region characterized by a strong lightning activity (up to 25 and 8 %, respectively, over central Africa in July) and a relative increase downwind of LNO_<i>x</i> emissions (up to 18 and 2 % for NO_<i>x</i> and O₃, respectively, in July). The calculated variability in NO_<i>x</i> and O₃ mixing ratios around the mean value according to the known uncertainties in the parameter estimates is at a maximum over continental tropical regions with ΔNO_<i>x</i> [−33.1, +29.7] ppt and ΔO₃ [−1.56, +2.16] ppb, in January, and ΔNO_<i>x</i> [−14.3, +21] ppt and ΔO₃ [−1.18, +1.93] ppb, in July, mainly depending on the determination of the diffusion properties of the atmosphere and the initial NO mixing ratio injected by lightning. This approach allows us (i) to reproduce a more realistic lightning NO_<i>x</i> chemistry leading to better NO_<i>x</i> and O₃ distributions on the large scale and (ii) to focus on other improvements to reduce remaining uncertainties from processes related to NO_<i>x</i> chemistry in CTM

Triarylamine based donor-acceptor systems for organics solar cells

National audienc

One step synthesis of D-A-D chromophores as active materials for organic solar cells by basic condensation

Donor-Acceptor-Donor conjugated systems are synthesized in good yield by double condensation of aromatic aldehydes of triarylamines with 2,3-diaminomaleonitrile under microwave activation with trifluoroacetic acid as catalyst. The electronic properties of the compounds are investigated and discussed and a first evaluation of their potential as donor material in organic photovoltaic cells is presented

Small Molecules for organic photovoltaic

Date du colloque : 05/2013</p