A Gibbs-Like Measure for Single-Time, Multi-Scale Energy Transfer in Stochastic Signals and Shell Model of Turbulence

2004 ◽  
Vol 114 (1/2) ◽  
pp. 137-154 ◽  
Author(s):  
Roberto Benzi ◽  
Luca Biferale ◽  
Mauro Sbragaglia
2016 ◽  
Vol 18 (5) ◽  
pp. 4134-4143 ◽  
Author(s):  
Linyin Yan ◽  
Yan Wan ◽  
Andong Xia ◽  
Sheng Hien Lin ◽  
Ran Huang

Multi-scale theoretical model and spectra simulation for dendrimers combining TD-DFT/DFT and semi-empirical methods.


1987 ◽  
Vol 42 (8) ◽  
pp. 813-818
Author(s):  
A. Kawski ◽  
J. Kamiński

A theory of the excitation energy transfer between like molecules in isotropic solution based on a centre or shell model of a primarily excited luminescent molecule and on the extended Förster “excitation master equation” has been elaborated. Fluorescence and phosphorescence depolarization are shown to be governed by singlet-singlet energy migration and described by the same expression. The comparison of the theoretical curve with the experimental data obtained by Gondo et al. (1975) for benzo[f]quinoline in ethanol glass at 77 K results in the following critical distance R0 for the excitation energy migration: 21.5 Å for fluorescence and phosphorescence, respectively.


Author(s):  
Andrey I. Musienko ◽  
Leonid I. Manevitch

We describe nonlinear dynamics of essentially non-homogeneous system of coupled oscillators using the technique of multi-scale expansions. The resonant mechanism of passive energy transfer from a massive oscillator into a light auxiliary one provides essential reduction of energy of the massive oscillator. Proposed active control algorithm increases noticeably the efficiency of energy transfer in comparison with passive control. The important advantage of this algorithm is that it provides a small consumption of energy. It is expedient to use our algorithm in the certain limits of parameters determined in the paper. This algorithm provides a necessary level of reduction of oscillator amplitude in a wide range of external perturbations.


1997 ◽  
Vol 71 (2) ◽  
pp. 177-188 ◽  
Author(s):  
Thomas Luxbacher ◽  
Harald P. Fritzer ◽  
Colin D. Flint

2005 ◽  
Vol 22 (11) ◽  
pp. 2877-2880 ◽  
Author(s):  
Fang Le ◽  
Cui Gui-Xiang ◽  
Xu Chun-Xiao ◽  
Zhang Zhao-Shun

1977 ◽  
Vol 32 (12) ◽  
pp. 1339-1343
Author(s):  
J. Kamiński ◽  
A. Kawski

Abstract Electronic Excitation Energy Transfer among like Molecules in Solution A theory of the excitation energy transfer among like (bomotransfer) molecules in solution, based on a shell model of the luminescent centre and on the assumptions given in our previous paper * is elaborated. Expressions for the time-dependent concentration depolarisation of the photo-luminescence (for emission anisotropy) in the sphere-and the shell-model are obtained. The expression for the concentration-dependent depolarisation is compared with the experimental results for five luminescent compounds in rigid cellulose acetate films. Good agreement was found with the equation which takes into account the excitation energy remigration.


1975 ◽  
Vol 30 (1) ◽  
pp. 15-20 ◽  
Author(s):  
A. Kawski ◽  
J. Kamiński

AbstractRadiationless energy transfer between like molecules (homotransfer) in thin rigid cellulose acetate films was studied by the concentration depolarization of the photoluminescence. The investigated substances are rhodamine B, 9-methylanthracene and 5-methyl-2-phenylindole. The experimental results have been compared with the “multi-shell model” of a luminescent centre. Good agreement was found with the equation which takes into account the excitation energy remigration. Concentration -depolarization measurements show that the critical distances R1, at which the probability of transfer of the excitation equals that of emission, are dependend on the excited wavelength. This is due to the failure of thermal relaxation of the exciting molecules with their environment.


2020 ◽  
Author(s):  
Andreas Albrecht ◽  
Julia Nowak ◽  
Peter Walla

Nature provides evidence that there is no fundamental limit for harvesting and funneling nearly all scattered sun-photons onto smaller conversion centers by ultra-fast emergy transfer processes. Recently, a proof-of-principle study showed that this can also be achieved by artificial systems containing light-harvesting pools of randomly oriented molecules that funnel energy to individual, aligned light-redirecting molecules.<br>However, capturing the entire solar spectrum requires engineering of complex multi-element structures considering macroscopic refraction and wave guiding of different spectral ranges of multijunction photovoltaics as well as ultrafast, nanoscopic light-harvesting, energy transfer and funneling, anisotropic absorption and emission and the spectra of a multitude of pigments of different orientations and concentrations. So far, no tool excited that allowed model such structures in one system.<br>Here we present a ray tracing tool allowing to model and analyze such multi-scale structures, including molecular, ultrafast energy transfer and funneling as well as anisotropic absorption and emission as well as micro-and macroscopic waveguiding and raytracing in one tool. We present first results of solar concentrator architectures with the highest theoretical energy conversion efficiency reported so far.<br>A novel tool is provided that allows to construct, model and analyze any desired complex ultrafast light-harvesting/photovoltaic architecture with the highest efficiencies by considering molecular, nanometric energy transfer and funneling as well as microscopic waveguiding and raytracing.


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