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4 th Hybrid and Organic Photovoltaic Conference -Uppsala 2012 168<br />

C51 - Oligomers and alternating copolymers designed for bulk heterojunction solar<br />

cells: synthesis, opto-electronic properties and device performances.<br />

Renaud Demadrille a , Zaireen Yahya a , Evan Spadafora a , Benjamin Grevin a , Mathieu Linares b ,<br />

Patrice Rannou a , Adam Pron a , Remi Debettignies c , Jean-Pierre Travers a<br />

a, CEA-INAC-SPRAM, 17 rue des Martyrs , Grenoble, 38054, FR<br />

b, Department of Computational Physics, IFM, Linkoping University, S-58183, Linkoping, Sweden, SE<br />

c, INES-CEA-RDI-DTS, Laboratoire Cellules Solaires, Le Bourget du Lac, Technolac Chambery, F-73370, France, FR<br />

Nanostructured bulk heterojunctions (BHJ) solar cells, which consist of pi-conjugated<br />

oligomers or polymers as electron donors and fullerenes as electron acceptors, are very<br />

promising in view of their relatively high power conversion efficiency. The inherent advantages<br />

of organic materials such as their light weight and low cost, and the possibility of fabricating<br />

large active area devices facilitated by their solution processability, have stimulated intensive<br />

research in this field during the last decade.<br />

Up to now, BHJ solar cells employing pi-conjugated oligomers or polymers have<br />

demonstrated power conversion efficiencies of ca. 6.7% and 8.3% respectively [1-2]. However,<br />

further improvement in the device performance could be expected, by developping new<br />

materials better matching the solar spectrum and more efficiently converting the sunlight to<br />

electricity.<br />

In the first part of this communication, we will discuss the design rules and the synthesis of<br />

new solution processable oligomers suitable for the use as active components in molecular BHJ<br />

solar cells. Their design is based on the combination of tailor-made oligothiophene segments<br />

as peripheral electron-donor subunits and indacenodithiophenone, benzothiadiazole or<br />

fluorenone as central electron-withdrawing units [3]. The use of this strategy which results in a<br />

significant extension of the absorption spectral range, affords the possibility to finely tune the<br />

energy levels position and the value of their band gap. We will discuss basic supramolecular<br />

chemistry concepts enabling the preparation of molecular nanowires [4-5] and the fabrication<br />

of nanostructured composites using these oligomers.<br />

Figure 1 Chemical structures of fluorenone-based oligomer and polymer studied in this work.<br />

In the second part, we will demonstrate that some of these oligomers can also be<br />

considered as smart building blocks to achieve the synthesis of copolymers showing perfectly<br />

controlled structures, well-suited for solar cells applications.<br />

In the final part, optoelectronic properties of the materials will be described in details and<br />

their electrical performances in devices will be discussed [6]. Promising reliminary results<br />

demonstrate high open circuit voltages (of ca. 0.8-0.9V) and power conversion efficiencies up<br />

to 2.2% for tested devices with an active area of 0.28 cm².<br />

© SEFIN 2012

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