Triplet Harvesting with a Simple Aromatic Carbonyl

被引:26
|
作者
Ziegenbein, Christian Torres [1 ]
Froebel, Sascha [1 ,2 ]
Gloess, Maria [1 ]
Nobuyasu, Roberto S. [3 ]
Data, Przemyslaw [3 ,4 ]
Monkman, Andrew [3 ]
Gilch, Peter [1 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Inst Phys Chem, Univ Str 1, D-40225 Dusseldorf, Germany
[2] Ohio State Univ, Dept Chem, 100 West 18th Ave, Columbus, OH 43210 USA
[3] Univ Durham, Dept Phys, Durham DH1 3LE, England
[4] Silesian Tech Univ, Fac Chem, M Strzody 9, PL-44100 Gliwice, Poland
关键词
aromatic carbonyls; fluorescence; OLED; time-resolved spectroscopy; triplet emitter; ACTIVATED DELAYED FLUORESCENCE; THIOXANTHONE FLUORESCENCE; EXCITED THIOXANTHONE; CHIMERIC BEHAVIOR; ENERGY-TRANSFER; MECHANISM; PHOSPHORESCENCE; PHOTOPHYSICS; XANTHONE;
D O I
10.1002/cphc.201700683
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The efficiency of organic light-emitting diodes crucially depends on triplet harvesters. These accept energy from triplet correlated electron hole pairs and convert it into light. Here, experimental evidence is given that simple aromatic carbonyls, such as thioxanthone, could serve this purpose. In these compounds, the emissive (1)* excitation may rapidly equilibrate with an upper triplet state ((3)n*). This equilibrium may persist for nanoseconds. Population of the (3)n* state via energy transfer from an electron hole pair should result in fluorescence emission and thereby triplet harvesting. To demonstrate the effect, solutions of 1,4-dichlorobenzene (triplet sensitizer) and thioxanthone (harvester) were excited at 266nm with a nanosecond laser. The emission decay reveals a 100ns decay absent in the thioxanthone only sample. This matches predictions for an energy transfer limited by diffusion and gives clear evidence that thioxanthone can convert triplet excitations into light.
引用
收藏
页码:2314 / 2317
页数:4
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