Journal
DYES AND PIGMENTS
Volume 96, Issue 2, Pages 391-396Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2012.08.028
Keywords
OLEDs; Thieno-[3,4-b]-pyrazine; Tetraphenylethylene; Red fluorescence; Non-doped device; Large Stokes shifts
Funding
- National Natural Science Foundation of China [21072026, 20923006]
- Ministry of Education for the New Century Excellent Talents in University [NCET-08-0074]
- Fundamental Research Funds for the Central Universities [DUT12ZD211]
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Two novel red fluorescent thieno-[3,4-b]-pyrazine-cored molecules containing tetraphenylethylene as peripheral groups, T-TP and T-TP1, are designed and synthesized. Their photophysical, electrochemical and electroluminescent properties are investigated. They are characterized by large Stokes shifts of over 100 nm. The bulky peripheral groups enable these molecules to be well soluble and provide the site-isolation effect on the planar emissive core. These novel materials are used as non-doped emitting layer to fabricate organic light-emitting diodes (OLEDs) by vacuum evaporation technique. Saturated red emission is obtained with a maximum brightness of 1385 cd m(-2) and a luminance efficiency of 0.66 cd A(-1). (C) 2012 Elsevier Ltd. All rights reserved.
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