Literature DB >> 19894231

Fullerene dimers (C60/C70) for energy harvesting.

Juan L Delgado1, Eva Espíldora, Moritz Liedtke, Andreas Sperlich, Daniel Rauh, Andreas Baumann, Carsten Deibel, Vladimir Dyakonov, Nazario Martín.   

Abstract

A new family of fullerene-based compounds, namely, soluble [60]- and [70]fullerene homodimers and the [60]/[70]heterodimer linked through 2-pyrazolino-pyrrolidino bridges, has been synthesised by simple procedures and in high yield. Electrochemical studies confirm their suitability to act as electron acceptors in combination with poly(3-hexylthiophene-2,5-diyl) (P3HT). Their optical properties in solution and in the solid state were studied. A significantly stronger absorption in [70]fullerene-containing dimers relative to [60]homodimer in solution in the visible range was observed. Furthermore, in all donor-acceptor blends studied an efficient charge transfer was observed by means of photoluminescence (PL), photoinduced absorption and light-induced electron spin resonance spectroscopy. The [70]homodimer was found to be a distinctive species, being the strongest PL quencher and most efficient acceptor with the longest lifetime of the charge-separated (polaron) states. As a consequence, bulk-heterojunction solar cells based on this novel [70]homodimer blended with P3HT demonstrated the highest quantum and power conversion efficiencies of 37 and 1 %, respectively, compared to those of [60]fullerene dimers.

Entities:  

Year:  2009        PMID: 19894231     DOI: 10.1002/chem.200902039

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Thioacetyl-terminated ferrocene-anthraquinone conjugates: synthesis, photo- and electrochemical properties triggered by protonation-induced intramolecular electron transfer.

Authors:  Wen-Wei Zhang; Mio Kondo; Takako Fujita; Kosuke Namiki; Masaki Murata; Hiroshi Nishihara
Journal:  Molecules       Date:  2010-01-04       Impact factor: 4.411

  1 in total

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