Phonon Sidebands, Multiphonon Relaxation of Excited States, and Phonon-Assisted Energy Transfer between Ions in Solids

1970 ◽  
Vol 1 (7) ◽  
pp. 2961-2969 ◽  
Author(s):  
Toru Miyakawa ◽  
D. L. Dexter
1990 ◽  
Vol 94 (11) ◽  
pp. 1253-1262 ◽  
Author(s):  
M. H. Alexander ◽  
A. Berning ◽  
A. Degli Esposti ◽  
A. Joerg ◽  
A. Kliesch ◽  
...  

1967 ◽  
Vol 159 (2) ◽  
pp. 262-266 ◽  
Author(s):  
L. A. Riseberg ◽  
W. B. Gandrud ◽  
H. W. Moos

2019 ◽  
Vol 205 ◽  
pp. 09034
Author(s):  
Minjung Son ◽  
Alberta Pinnola ◽  
Roberto Bassi ◽  
Gabriela S. Schlau-Cohen

We utilise ultrabroadband two-dimensional electronic spectroscopy to map out pathways of energy flow in LHCII across the entire visible region. In addition to the well-established, low-lying chlorophyll Qy bands, our results reveal additional pathways of energy relaxation on the higher-lying excited states involving the S2 energy levels of carotenoids, including ultrafast carotenoid-to-chlorophyll energy transfer on 90-150 fs timescales.


The dependences on concentration of the yield of excited triplet naphthalene, G ( 3 Naph٭), and of the radiation-induced fluorescence obtained on pulse radiolysis of solutions of naphthalene in cyclopentane, cyclooctane and decalin are reported. The yields of singlet excited naphthalene, G( 1 Naph٭), formed on pulse radiolysis of these solutions have been determined by comparing the intensity of the radiation-induced fluorescence with that obtained on photo excitation and the extent of formation of 3 Naph٭ by intersystem crossing, G ( 3 Naph٭) i. s. c., is assessed. Upper limit yields of solvent excited states, G ( 1 RH٭), were determined by measuring the extent of singlet energy transfer to toluene. It is concluded that energy transfer from solvent excited states plays a minor role in the formation of excited states of aromatic solutes.


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