Fullerene Dimers (C60/C70) for Energy Harvesting

被引:65
作者
Delgado, Juan L. [2 ,3 ]
Espildora, Eva [2 ]
Liedtke, Moritz [1 ]
Sperlich, Andreas [4 ]
Rauh, Daniel [1 ]
Baumann, Andreas [4 ]
Deibel, Carsten [4 ]
Dyakonov, Vladimir [1 ,4 ]
Martin, Nazario [2 ,3 ]
机构
[1] Bavarian Ctr Appl Energy Res ZAE Bayern, D-97074 Wurzburg, Germany
[2] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Organ, E-28040 Madrid, Spain
[3] Univ Autonoma Madrid, Fac Ciencias, IMDEA Nanociencia, E-28049 Madrid, Spain
[4] Univ Wurzburg, D-97074 Wurzburg, Germany
关键词
charge transfer; dimerization; energy conversion; EPR spectroscopy; fullerenes; POLYMER SOLAR-CELLS; ORGANIC PHOTOVOLTAICS; AZOMETHINE YLIDES; POLYFLUORENE; EFFICIENT; CYCLOADDITION; EXCITATIONS; PERFORMANCE; FAMILY;
D O I
10.1002/chem.200902039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new family of fullerenebased 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.
引用
收藏
页码:13474 / 13482
页数:9
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