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Reorientation Dynamics of Chromophores in Photosensitive Polymers by Means of Coarse‐Grained Modeling
Author(s) -
Ilnytskyi Jaroslav M.,
Saphiannikova Marina
Publication year - 2015
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201500500
Subject(s) - chromophore , azobenzene , photoisomerization , polymer , materials science , chemical physics , molecular dynamics , relaxation (psychology) , dynamics (music) , anisotropy , orientation (vector space) , population , wavelength , molecular physics , chemistry , optics , computational chemistry , isomerization , photochemistry , physics , composite material , optoelectronics , organic chemistry , mathematics , sociology , acoustics , psychology , social psychology , geometry , catalysis , demography
We study the photoisomerization of azobenzene chromophores embedded into a polymer matrix by using coarse‐grained simulations. Two types of beads are considered: t‐ and c‐beads, which are rich in trans and cis isomers, respectively. Simulations combine deterministic (molecular dynamics) and stochastic (random‐type switching) parts. The ratio between the characteristic times for photoinduced reorientation and for orientation relaxation is tuned to be of the order found in experiments. The essential features of the phenomenon: 1) the existence of a stationary state, and 2) anisotropic distribution of the orientations of t‐beads (orientation hole‐burning effect), are reproduced. We study population dynamics of c‐beads and the strength of the orientation hole burning, depending on the illumination wavelength and its intensity. The form of the reorientation potential of the mean force acting on the t‐beads is analyzed and its use is validated.
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