scholarly journals The role of charge-transfer states in energy transfer and dissipation within natural and artificial bacteriochlorophyll proteins

2014 ◽  
Vol 5 (1) ◽  
Author(s):  
Md. Wahadoszamen ◽  
Iris Margalit ◽  
Anjue Mane Ara ◽  
Rienk van Grondelle ◽  
Dror Noy
2015 ◽  
Vol 2015 (18) ◽  
pp. 3019-3027 ◽  
Author(s):  
Yolanda C. Miranda ◽  
Leide L. A. L. Pereira ◽  
José H. P. Barbosa ◽  
Hermi F. Brito ◽  
Maria C. F. C. Felinto ◽  
...  

2020 ◽  
Vol 8 (26) ◽  
pp. 8823-8839
Author(s):  
Maksym Buryi ◽  
Lubomír Havlák ◽  
Vítězslav Jarý ◽  
Jan Bárta ◽  
Valentyn Laguta ◽  
...  

Several sets of Eu-doped Y3Al5O12 (YAG) ceramic samples were synthesized by the vacuum sintering technique. Absorption bands at 250, 370 and 550 nm in samples were attributed to the charge transfer transition in the EuY2+ + F+ pair center.


2001 ◽  
Vol 16 (9) ◽  
pp. 2568-2571 ◽  
Author(s):  
J. K. Park ◽  
C. H. Kim ◽  
K. J. Choi ◽  
H. D. Park ◽  
S. Y. Choi

The purpose of this study is to develop an understanding of the photoluminescence properties of Al3+, Pr3+ doped perovskite-type La2/3TiO3 and pyrochlore-type La2Ti2O7 phosphor, which is characterized by the red emission (1D2 →3H4 transition) of the Pr3+ ion. The explanation for the energy transfer and the corresponding critical distance is proposed on the basis of the role of Al3+ ions in the perovskite-type La2/3TiO3:Pr phosphor. To clarify the distinction of photoluminescence properties between the perovskite-type La2/3TiO3 and the pyrochlore-type La2Ti2O7, the trap-involved process and the charge transfer band have been investigated, respectively.


Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1623
Author(s):  
Anton A. Babaev ◽  
Anastasiia V. Sokolova ◽  
Sergei A. Cherevkov ◽  
Kevin Berwick ◽  
Alexander V. Baranov ◽  
...  

PL intensity quenching and the PL lifetime reduction of fluorophores located close to graphene derivatives are generally explained by charge and energy transfer processes. Analyzing the PL from PbS QDs in rGO/QD systems, we observed a substantial reduction in average PL lifetimes with an increase in rGO content that cannot be interpreted solely by these two processes. To explain the PL lifetime dependence on the rGO/QD component ratio, we propose a model based on the Auger recombination of excitations involving excess holes left in the QDs after the charge transfer process. To validate the model, we conducted additional experiments involving the external engineering of free charge carriers, which confirmed the role of excess holes as the main QD PL quenching source. A mathematical simulation of the model demonstrated that the energy transfer between neighboring QDs must also be considered to explain the experimental data carefully. Together, Auger recombination and energy transfer simulation offers us an excellent fit for the average PL lifetime dependence on the component ratio of the rGO/QD system.


1973 ◽  
Vol 51 (11) ◽  
pp. 1881-1884 ◽  
Author(s):  
R. O. Loutfy ◽  
R. W. Yip

The rate constants for quenching of triplet acetone by a series of halobenzenes have been determined by flash emission technique. Quenching was found to be approximately a hundred times faster than that for triplet benzophenone. For both triplet ketones, quenching did not decrease with the increase in triplet energy difference between ketone and quencher (as expected for normal endothermic triplet energy transfer) and did not correlate with the i.p. of all of the quenchers studied. All of the qualitative features of the quenching results can be simply interpreted in terms of enhanced coupling of the locally excited triplet ketone and quencher states as a result of interaction with the charge transfer state.


Author(s):  
Weidong Qiu ◽  
Xinyi Cai ◽  
Mengke Li ◽  
Liangying Wang ◽  
Yanmei He ◽  
...  

Dynamic adjustment of emission behaviours by controlling the extent of twisted intramolecular charge transfer character in excited state.


2011 ◽  
Vol 35 (1) ◽  
pp. 15-27
Author(s):  
Zoran Ivić ◽  
Željko Pržulj

Adiabatic large polarons in anisotropic molecular crystals We study the large polaron whose motion is confined to a single chain in a system composed of the collection of parallel molecular chains embedded in threedimensional lattice. It is found that the interchain coupling has a significant impact on the large polaron characteristics. In particular, its radius is quite larger while its effective mass is considerably lighter than that estimated within the one-dimensional models. We believe that our findings should be taken into account for the proper understanding of the possible role of large polarons in the charge and energy transfer in quasi-one-dimensional substances.


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