Ultralong Single Organic Semiconducting Nano/Microwires Based on Spiro-Substituted Perylenetetracarboxylic Diimide
Source abstract
Abstract
An ultralong single organic semiconducting nano/microwire (NMW) is difficult to obtain. Here we show that this NMW can easily be prepared by using drying under solvent atmosphere method. This technique is not only unique, but also very compatible with our active material, spiro-substituted perylenetetracarboxylic diimide. A single NMW with a length of up to ∼5.5 mm and an aspect ratio of ∼9200 can be obtained. Finally, we succeeded to measure the electrical resistivity of a single NMW with values between 1 × 10(2) and 1 × 10(4) Ω m and the growth direction can be controlled as well by using a prestructured substrate.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Molecular Junctions and Nanostructures
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Macromolecular Chemistry and Molecular Materials (mmCmm), Department of Mathematics and Science and Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel, Heinrich-Plett-Strasse 40, D 34132, Kassel, Germany
References (22)
Show source-provided references
1. Duan X. · Nature · 2003 · 425 · 27410.1038/nature01996 ↗
2. Zach M. P. · Science · 2000 · 290 · 212010.1126/science.290.5499.2120 ↗
3. Greiner A. · Angew. Chem., Int. Ed. · 2007 · 46 · 567010.1002/anie.200604646 ↗
4. Chiu J. J. · Adv. Mater. · 2003 · 15 · 136110.1002/adma.200304918 ↗
5. De Luca G. · Adv. Funct. Mater. · 2007 · 17 · 379110.1002/adfm.200700549 ↗
6. Che Y. · J. Am. Chem. Soc. · 2007 · 129 · 723410.1021/ja071903w ↗
7. Balakrishnan K. · J. Am. Chem. Soc. · 2006 · 128 · 739010.1021/ja061810z ↗
8. Balakrishnan K. · J. Am. Chem. Soc. · 2005 · 127 · 1049610.1021/ja052940v ↗
9. Zang L. · Acc. Chem. Res. · 2008 · 41 · 159610.1021/ar800030w ↗
10. Che Y. · J. Am. Chem. Soc. · 2007 · 129 · 635410.1021/ja070164g ↗
11. Che Y. · J. Am. Chem. Soc. · 2010 · 132 · 574310.1021/ja909797q ↗
12. Datar A. · Chem. Commun. · 2006 · 164910.1039/b518060k ↗
13. Briseno A. L. · Nano Lett. · 2007 · 7 · 66810.1021/nl0627036 ↗
14. Briseno A. L. · Nano Lett. · 2007 · 7 · 284710.1021/nl071495u ↗
15. Su W. · ChemPhysChem. · 2007 · 8 · 185710.1002/cphc.200700246 ↗
16. Saragi T. P. I. · Chem. Rev. · 2007 · 107 · 101110.1021/cr0501341 ↗
17. Onken, K.Ph.D. Thesis,University of Kassel,Germany, 2007.
18. Che Y. · Nano Lett. · 2008 · 8 · 221910.1021/nl080761g ↗
19. Kim D. H. · Adv. Mater. · 2006 · 18 · 71910.1002/adma.200502442 ↗
20. O’Brien G. A. · Adv. Mater. · 2006 · 18 · 237910.1002/adma.200601012 ↗
21. Zhou Y. · Adv. Mater. · 2008 · 19 · 3749
22. Guo Y. · J. Am. Chem. Soc. · 2008 · 130 · 919810.1021/ja8021494 ↗