Journal of Materials Chemistry · 2010 · 27 citations · 24 references
Natural SciencesChemistryMaterials ScienceElectronic MaterialsPolymer ChemistrySemiconductor MaterialsOrganic Electronic MaterialsOrganic SemiconductorsPhotovoltaic DevicesPhotovoltaic MaterialsSolar Cell MaterialsSolar CellsBulk Heterojunction Solar CellsHeterojunction Solar CellsMild Reaction ConditionsOrganic Photovoltaic CellsOrganic Photovoltaic MaterialsOrganic PhotovoltaicsOrganic Solar CellsPower Conversion
[6,6]-Thienyl-C61-butyric acid ester derivatives with methyl, hexyl and 2-ethylhexyl at the 5-position of thiophene ring (TCBM-Cn, n represents the number of carbon atom in the alkyl chain) were synthesized. Unlike [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), these methanofullerene derivatives ([6,6] adduct) can be directly obtained from the typical diazo addition under mild conditions, and high temperature isomerization is unnecessary. With a hexyl or 2-ethylhexyl group at the 5-position of thiophene, the solubility of TCBM-Cn in chlorobenzene is as high as 180 ± 10 mg ml−1. Bulk heterojunction photovoltaic solar cells were fabricated with a device structure of ITO/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/poly(3-hexylthiophene) (P3HT) : TCBM-Cn (1 : 0.8 w/w)/LiF/Al. The device based-on TCBM-C6 exhibited the best performance with a power conversion efficiency (PCE) of up to 4.26%.
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Christoph J. Brabec, Niyazi Serdar Sariçiftçi, J.C. Hummelen · Advanced Functional Materials · 2001 · 3.8K citations · Full text
Conjugated Polymer Photovoltaic Cells
Kevin M. Coakley, Michael D. McGehee · Chemistry of Materials · 2004 · 2.1K citations
Natural Sciences, Materials Engineering, Materials Science +17
Origin of the Open Circuit Voltage of Plastic Solar Cells
Christoph J. Brabec, Antonio Cravino, Niyazi Serdar Sariçiftçi et al. · Advanced Functional Materials · 2001 · 1.8K citations · Full text