Letters to Nature
Nature 395, 151-154 (10 September 1998) | doi:10.1038/25954; Received 20 April 1998; Accepted 24 June 1998
Highly efficient phosphorescent emission from organic electroluminescent devices
M. A. Baldo1, D. F. O'Brien1, Y. You2, A. Shoustikov2, S. Sibley2,3, M. E. Thompson2 & S. R. Forrest1
- Center for Photonics and Optoelectronic Materials, Department of Electrical Engineering and the Princeton Materials Institute, Princeton University, Princeton, New Jersey 08544, USA
- Department of Chemistry, University of Southern California, Los Angeles, California 90089, USA
- Permanent address: Department of Chemistry, Goucher College, Baltimore, Maryland 21204-2794, USA.
Correspondence to: S. R. Forrest1 Correspondence and requests for materials should be addressed to S.R.F. (forrest@ee.princeton.edu).
The efficiency of electroluminescent organic light-emitting devices1,2 can be improved by the introduction3 of a fluorescent dye. Energy transfer from the host to the dye occurs via excitons, but only the singlet spin states induce fluorescent emission; these represent a small fraction (about 25%) of the total excited-state population (the remainder are triplet states). Phosphorescent dyes, however, offer a means of achieving improved light-emission efficiencies, as emission may result from both singlet and triplet states. Here we report high-efficiency (
90%) energy transfer from both singlet and triplet states, in a host material doped with the phosphorescent dye 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphine platinum(II) (PtOEP). Our doped electroluminescent devices generate saturated red emission with peak external and internal quantum efficiencies of 4% and 23%, respectively. The luminescent efficiencies attainable with phosphorescent dyes may lead to new applications for organic materials. Moreover, our work establishes the utility of PtOEP as a probe of triplet behaviour and energy transfer in organic solid-state systems.


