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Robust Circular Polarized Emission from Nanoscopic Single-Molecule Sources: Application to Solid State Devices

Published online by Cambridge University Press:  26 February 2011

Ruthanne Hassey ,
Ellen J Swain ,
Nathan I Hammer ,
Emily L Richards ,
Dhandapani Venkataraman  and
Michael D Barnes
Ruthanne Hassey
Affiliation:
[email protected], University of Massachusetts, Chemistry, 710 North Pleasant, Amherst, MA, 01003, United States
Ellen J Swain
Affiliation:
[email protected], University of Massachusetts, Chemistry, 710 North Pleasant, Amherst, MA, 01003, United States
Nathan I Hammer
Affiliation:
[email protected], University of Massachusetts, Chemistry, 710 North Pleasant, Amherst, MA, 01003, United States
Emily L Richards
Affiliation:
[email protected], University of Massachusetts, Chemistry, 710 North Pleasant, Amherst, MA, 01003, United States
Dhandapani Venkataraman
Affiliation:
[email protected], University of Massachusetts, Chemistry, 710 North Pleasant, Amherst, MA, 01003, United States
Michael D Barnes
Affiliation:
[email protected], University of Massachusetts, Chemistry, 710 North Pleasant, Amherst, MA, 01003, United States
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Abstract

Controlling the polarization state of fluorescence emission in solid state devices is an important goal in optical display technologies. High-purity (right or left) circular polarized emission is particularly desirable because an arbitrary linearly polarized state can be generated with much higher efficiency (lower loss) as compared with a non-polarized fluorescence input. Here we discuss observation of resonant chiroptical effects (fluorescence detected circular dichroism (FDCD), and circular polarized luminescence (CPL)) from single (bridged-triarylamine) helicene molecules in a solid-film format. In the FDCD experiment using 457-nm excitation – an excitation wavelength where the bulk circular dichroism is negligible – single-molecule fluorescence from enantiomerically pure helicene samples show surprising distribution of dissymmetry (g) parameters centered near zero but with a significant contribution from molecules showing an almost perfectly pure response to either right or left circularly polarized light. Experiments combining a well-defined circularly polarized excitation (either right or left) with decomposition of the fluorescence into left- and right-circular polarization component show only a weak correlation between the dissymmetry (sign and magnitude) of the CPL with the polarization state of the input. Current efforts are directed at wavelength resolved CPL, FDCD at wavelengths that are more closely match to bulk circular dichroism features, and orientational dependence of FDCD and CPL. These results provide new insight into chiroptical properties of chiral fluorophores at the single molecule level and suggests new optical device possibilities with chiral fluorophores.

Keywords

optoelectronicdevicesoptical properties
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 965: Symposium S – Organic Electronics – Materials, Devices and Applications , 2006 , 0965-S12-08
Copyright
Copyright © Materials Research Society 2007

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References

REFERENCES

1. Dyreklev, P., Berggren, M., Inganäs, O., Andersson, M. R., Wennerström, O., and Hjertberg, T., Adv. Mater. 7, 43 (1995).Google Scholar
2. Grell, M. and Bradley, D. C., Adv. Mater. 11, 895 (1999).Google Scholar
3. Grell, M., Oda, M., Whitehead, K. S., Asimakis, A., Neher, D., and Bradley, D. C., Adv. Mater. 13, 577 (2001).Google Scholar
4. Chen, S. H., Katsis, D., Schmid, A. W., Mastrangelo, J. C., Tsutsui, T., and Blanton, T. N., Nature 397, 506 (1999).Google Scholar
5. Feringa, B. L. and Delden, R. A. van, Angew. Chem., Int. Ed. 38, 3418 (1999).Google Scholar
6. Sato, I., Yamashima, R., Kadowaki, K., Yamamoto, J., Shibata, T., and Soai, K., Angew. Chem., Int. Ed. 40, 1096 (2001).Google Scholar
7. Field, J. E., Muller, G., Riehl, J. P., Venkataraman, D., J. Am. Chem. Soc. 125, 11808 (2003).Google Scholar
8. Field, J. E., Hill, T. J., Venkataraman, D., J. Org. Chem. 68, 6071 (2003).Google Scholar
9. Odoi, M. Y., Hammer, N. I., Sill, K., Emrick, T., Barnes, M. D., J. Am. Chem. Soc. 128, 3506 (2006).Google Scholar
10. Hammer, N. I., Early, K. T., Sill, K., Odoi, M. Y., Emrick, T., and Barnes, M. D., J. Phys. Chem. B 110, 14167 (2006).Google Scholar