2004
DOI: 10.1080/15421400490439103
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Organic Heterojunction Photovoltaic Cells Made of Discotic, Mesogenic Materials

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Cited by 21 publications
(10 citation statements)
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“…One example that is very closely related to that described here is liquid-crystalline tetraester derivatives of perylene, coronene and ovalene 23 that have been used as n-type liquid-crystalline semiconductors for OLEDs and heterojunction solar cells. 24,25 Further relevant transformations may include synthesis of star-shaped derivatives of HBC that are prepared via Sonogashira coupling of the hexaiodo precursor with appropriate alkyl-or alkylaryl-acetylenes. 26 In all such cases, one may expect that utilization of a mixture of reagents will result in the mixtures of products with variable, well-defined compositions, and will thus provide a way for the ''fine-tuning'' of their thermotropic properties.…”
Section: Discussionmentioning
confidence: 99%
“…One example that is very closely related to that described here is liquid-crystalline tetraester derivatives of perylene, coronene and ovalene 23 that have been used as n-type liquid-crystalline semiconductors for OLEDs and heterojunction solar cells. 24,25 Further relevant transformations may include synthesis of star-shaped derivatives of HBC that are prepared via Sonogashira coupling of the hexaiodo precursor with appropriate alkyl-or alkylaryl-acetylenes. 26 In all such cases, one may expect that utilization of a mixture of reagents will result in the mixtures of products with variable, well-defined compositions, and will thus provide a way for the ''fine-tuning'' of their thermotropic properties.…”
Section: Discussionmentioning
confidence: 99%
“…119 Perylene tetraesters 66 with linear substituents form columnar mesophases with reasonably low melting points 120 and have been used for the fabrication of OLEDs 121 and photovoltaic solar cells. 122 The tetraesters with 2-ethylhexyl substituents 66, 67 and 68 (Fig. 12, 13) form columnar mesophases at room temperature and have clearing points at 260 uC, 153 uC, and .375 uC respectively.…”
Section: Low-symmetry Discotic Moleculesmentioning
confidence: 99%
“…[5][6][7] These electronic properties together with their solubility and film forming properties qualify them for low cost solution processing of organic electronic devices. [8][9][10][11][12][13][14][15][16] Formation and alignment of monodomains over 100 mm length scales have been demonstrated for several DLCs albeit the alignment of the columnar stacks perpendicular to a substrate (homeotropic) is more difficult to achieve than parallel to a substrate (homogeneous). 1,2,17 Equally important to self-organization and alignment are the electronic properties of the DLC molecules, such as their red/ox potentials and frontier orbital energies, as they define charge transport across interfaces to electrodes and other materials in electronic devices.…”
Section: Introductionmentioning
confidence: 99%