Feb. 17, 2013 — Organic electronics has already hit the market in smart-phone displays and holds great promise for future applications like flexible electroluminescent foils (a potential replacement for conventional light bulbs) or solar cells that convert sunlight to electricity. A reoccurring problem in this technology is to establish good electrical contact between the active organic layer and metal electrodes. Organic molecules are frequently used also for this purpose. Until now, however, it was practically impossible to accurately predict which molecules performed well on the job. They basically had to be identified by trial-and-error.
Now, an international team of scientists working with Dr. Georg Heimel and Prof. Norbert Koch from the HZB and the Humboldt University Berlin has unraveled the mystery of what these molecules have in common. Their discovery enables more focused improvements to contact layers between metal electrodes and active materials in organic electronic devices.
"We have been working on this question for a number of years now and could at last come up with a conclusive picture using a combination of several experimental methods and theoretical calculations," Georg Heimel explains. The researchers systematically examined different types of molecules whose backbones consist of the same chain of fused aromatic carbon rings. They differed in just one little detail: the number of oxygen atoms projecting from the backbone. These modified molecules were placed on the typical contact metals gold, silver, and copper.
Using photoelectron spectroscopy (UPS and XPS) at HZB's own BESSY II synchrotron radiation source, the researchers were able to identify Chemical-Bonds'>chemical bonds that formed between the metal surfaces and the molecules as well as to measure the energy levels of the conduction electrons. Colleagues from Germany's Tübingen University determined the exact distance between the molecules and the metal surfaces using x-ray standing wave measurements taken at the ESRF synchrotron radiation source in Grenoble, France.
These experiments showed that, upon contact between the oxygen atoms protruding from the backbone and several of the metals, the molecules' internal structure changed in such a way that they lost their semiconducting properties and instead adopted the metallic properties of the surface. Despite similar prerequisites, this effect was not observed for the "bare"-backbone molecule. From the observation which molecules underwent these kinds of drastic changes on what metal, the researchers could derive general guidelines. "At this point, we have a pretty good sense of how molecules ought to look like and what their properties should be if they are to be good mediators between active organic materials and metal contacts, or, as we like to call it, good at forming soft metallic contacts," says Heimel.
- G. Heimel, S. Duhm, I. Salzmann, A. Gerlach, A. Strozecka, J. Niederhausen, C. Bürker, T. Hosokai, I. Fernandez-Torrente, G. Schulze, S. Winkler, A. Wilke, R. Schlesinger, J. Frisch, B. Bröker, A. Vollmer, B. Detlefs, J. Pflaum, S. Kera, K. J. Franke, N. Ueno, J. I. Pascual, F. Schreiber, N. Koch. Charged and metallic molecular monolayers through surface-induced aromatic stabilization. Nature Chemistry, 2013; DOI: 10.1038/NCHEM.1572
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