Zusammenhang zwischen Schweratominduzierter Fluoreszenzlöschung und Termschema von mehrkernigen aromatischen Kohlenwasserstoffen / Correlation between Heavy-atom induced Fluorescence Quenching and Energy Levels of Polynuclear Aromatic Hydrocarbons

1973 ◽  
Vol 28 (10) ◽  
pp. 1743-1744
Author(s):  
H. Dreeskamp ◽  
M. Zander

The observation that the fluorescence of certain polynuclear aromatic hydrocarbons (perylene, 1.2 ;5.6-dibenzoperylene, 9.10-diphenylanthracene and rubrene) is quenched by alkyl iodides only slightly is explained on the basis of the energy levels of these hydrocarbons. In these systems an effective radiationless desactivation of the fluorescing state S1 by intersystem crossing into the triplet manifold is prevented by a wide energy gap between S1 and the lowest triplet state, and the absence of excited triplet states below s,.

2007 ◽  
Vol 111 (2) ◽  
pp. 1024-1028 ◽  
Author(s):  
Yosuke Oseki ◽  
Mamoru Fujitsuka ◽  
Masanori Sakamoto ◽  
Xichen Cai ◽  
Tetsuro Majima

2020 ◽  
Vol 124 (38) ◽  
pp. 20816-20826
Author(s):  
Ruifang Wang ◽  
Taiping Hu ◽  
Yanwei Liu ◽  
Xiaofang Wei ◽  
Jianjun Liu ◽  
...  

2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Kati Stranius ◽  
Manuel Hertzog ◽  
Karl Börjesson

Abstract Strong coupling between light and matter leads to the spontaneous formation of hybrid light–matter states, having different energies than the uncoupled states. This opens up for new ways of modifying the energy landscape of molecules without changing their atoms or structure. Heavy metal-free organic light emitting diodes (OLED) use reversed intersystem crossing (RISC) to harvest light from excited triplet states. This is a slow process, thus increasing the rate of RISC could potentially enhance OLED performance. Here we demonstrate selective coupling of the excited singlet state of Erythrosine B without perturbing the energy level of a nearby triplet state. The coupling reduces the triplet–singlet energy gap, leading to a four-time enhancement of the triplet decay rate, most likely due to an enhanced rate of RISC. Furthermore, we anticipate that strong coupling can be used to create energy-inverted molecular systems having a singlet ground and lowest excited state.


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