Abstract
In this work, the synthesis of an oligothiophene having a donor–acceptor–donor (D–A–D) chromophore with hydrogen bonding groups is described. The D–A–D molecule was demonstrated to self-organize via intermolecular H-bonding between barbituric acid units. Interactions between the oligothiophene subunits were also found to be important, affording nanoribbons that could be observed by atomic force and transmission electron microscopy. The applicability of the oligothiophene for organic electronic applications was investigated by fabricating organic field-effect transistors (OFETs) and organic photovoltaic devices. The OFET measurements yielded p-type mobility of 7 × 10–7 cm2/(V s), and when blended with C60-PCBM, the photovoltaic efficiency was observed to be 0.18%.
| Original language | English |
|---|---|
| Journal | Journal of Physical Chemistry Part C: Nanomaterials and Interfaces |
| Volume | 115 |
| Issue number | 29 |
| Pages (from-to) | 14369-14376 |
| ISSN | 1932-7447 |
| DOIs | |
| Publication status | Published - 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Polymer solar cells
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