Antoine Mirloup

High-Performance Solution-Processed Solar Cells and Ambipolar Behavior in Organic Field-Effect Transistors with Thienyl-BODIPY Scaffoldings

Green-absorbing dipyrromethene dyes engineered from bis-vinyl-thienyl modules are planar molecules, exhibiting strong absorption in the 713-724 nm range and displaying comparable electron and hole mobilities in thin films (maximum value 1 × 10(-3) cm(2)/(V·s)). Bulk heterojunction solar cells assembled with these dyes and a fullerene derivative (PC(61)BM) at a low ratio give a power conversion efficiency as high as 4.7%, with short-circuit current values of 14.2 mA/cm(2), open-circuit voltage of 0.7 V, and a broad external quantum efficiency ranging from 350 to 920 nm with a maximum value of 60%.

Thiazole-based scaffolding for high performance solar cells

An interesting way of decreasing both HOMO and LUMO energy levels simultaneously while keeping the band-gap constant in soluble electron-donor small molecules for photovoltaic applications is presented. This consists in the replacement of thiophene rings by thiazole units in small molecules based on the alternation of electron-rich and electron-deficient moieties. A new diketopyrrolopyrrole-based dumbbell-shaped electron-donor soluble molecule for organic photovoltaic applications has been synthesized and characterized. It includes thiazole units as linkers between the bis-lactam core and the triazatruxene moieties used as π-stacking platforms. A power conversion efficiency of 6.3% has been attained with this thiazole derivative and in particular with an increase of the open-circuit voltage of 0.15 V with respect to the thiophene-based organic semiconducting counterpart. This open-circuit voltage increase is due to the lowering of the HOMO level of the thiazole derivative while its LUMO level has also been stabilized as highlighted by the similar band-gap measured for the thiazole and thiophene derivatives.

A deep-purple-grey thiophene–benzothiadiazole–thiophene BODIPY dye for solution-processed solar cells

In this work we explore the synthesis of an extended 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene dye (BODIPY) engineered from thiophene–benzothiadiazole–thiophene modules linked in the 3,5-substitution positions. We found that this highly soluble dye absorbs up to 800 nm in solution and up to 900 nm in thin films. An effective charge transfer absorption band was found at around 479 nm. The hybrid dye emits at 778 nm with a quantum yield of about 6%. Similar electrochemical and optical gaps were determined about 1.36 eV. When deposited in thin films the dye exhibits an ambipolar nature with well-balanced hole and electron mobilities. Bulk heterojunction solar cells based upon this dye blended with [6,6]phenylC61or71butyricacid methylester (PC61BM or PC71BM) provide a power conversion efficiency of about 1.26% upon a mild thermal annealing.

Rational Engineering of BODIPY-Bridged Trisindole Derivatives for Solar Cell Applications

Boron dipyrromethene (BODIPY) and its derivatives are known to be efficient photon-harvesting chromophores. However, their study as active materials in bulk heterojunction (BHJ) solar cells is still scarce. In this study, the development of new synthetic ways to design original BODIPY-based dumbbell-shape molecules, including a first 2,3,5,6-tetravinyl aromatic BODIPY molecule, is reported. High fill factors can be obtained in BHJ solar cells when blended with a fullerene derivative, leading to a new record BODIPY-based power conversion efficiency of 5.8 %.

Design, synthesis and photochemical properties of the first examples of iminosugar clusters based on fluorescent cores

Summary The synthesis and photophysical properties of the first examples of iminosugar clusters based on a BODIPY or a pyrene core are reported. The tri- and tetravalent systems designed as molecular probes and synthesized by way of Cu(I)-catalysed azide–alkyne cycloadditions are fluorescent analogues of potent pharmacological chaperones/correctors recently reported in the field of Gaucher disease and cystic fibrosis, two rare genetic diseases caused by protein misfolding.

Panchromatic absorption of dye sensitized solar cells by co-Sensitization of triple organic dyes

Dye sensitized solar cells (DSSCs) were co-sensitized with three custom molecularly engineered organic dyes containing butyloxyl chain induced dye (Y1), boron dipyrromethene (bodipy) dye (TP2A), and squaraine (SQ) ring configured dye (HSQ4). The individual power conversion efficiencies of the DSSCs sensitized with Y1, TP2A and HSQ4 sensitizers were 3.44%, 4.26% and 5.78%, respectively. Co-sensitized TP2A + HSQ4 dyes at a 2 : 1 molar ratio showed an efficiency of 7.02%. Further addition of Y1 dye with optimal TP2A + HSQ4 increased the VOC from 0.580 V to 0.605 V. The co-sensitized Y1 + TP2A + HSQ4 based DSSCs showed a new optimal efficiency (η) of 7.48%. This is the highest efficiency recorded for DSSCs based on co-sensitization of triple organic dyes. Intensity modulated photovoltage spectroscopy further confirms the longer lifetime of co-sensitized Y1 + TP2A + HSQ4 compared to that of each individual TP2A and HSQ4 and co-sensitized TP2A + HSQ4 dye.

Dye-sensitized solar cells: Sensitized with triple dyes in ultraviolet to near infrared

Co-sensitization of triple dyes for panchromatic absorption is rare in literature, here we present a dye sensitized solar cell (DSSCs) co-sensitized with molecular engineered organic butyloxyl chain induced Y1 dye, bodipy dye TP2A, and squaraine based dye SQ1. The co-sensitized TP2A+SQ1 showed efficiency of 5.60%. This co-sensitized triple dies shows a wide range of absorption spectrum from 300nm-800nm region under 1 sunlight illumination (100 mW/cm2) in DSSCs operation. By controlling the volumetric ratio a high photocurrent density (JSC) of 14.59 mAcm-2 and 0.703 fill factor were achieved. This yielded to an impressive efficiency of 6.21% for Y1+TP2A+SQ1 co-sensitized dyes, which is higher than that of each individual dyes. It was also observed that the efficiency of co-sensitized triple dyes is higher than co-sensitized of TP2A+SQ1 in solar cells.