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|Title:||Energy transfer dynamics in trimers and aggregates of light-harvesting complex II probed by 2D electronic spectroscopy||Authors:||Enriquez, Miriam Grace Mangubat
Lambrev, Petar H.
|Keywords:||DRNTU::Science::Chemistry::Physical chemistry||Issue Date:||2015||Source:||Enriquez, M. G. M., Akhtar, P., Zhang, C., Garab, G., Lambrev, P. H., & Tan, H.-S. (2015). Energy transfer dynamics in trimers and aggregates of light-harvesting complex II probed by 2D electronic spectroscopy. Journal of chemical physics, 142(21), 212432-.||Series/Report no.:||Journal of chemical physics||Abstract:||The pathways and dynamics of excitation energy transfer between the chlorophyll (Chl) domains in solubilized trimeric and aggregated light-harvesting complex II (LHCII) are examined using two-dimensional electronic spectroscopy (2DES). The LHCII trimers and aggregates exhibit the unquenched and quenched excitonic states of Chl a, respectively. 2DES allows direct correlation of excitation and emission energies of coupled states over population time delays, hence enabling mapping of the energy flow between Chls. By the excitation of the entire Chl b Qy band, energy transfer from Chl b to Chl a states is monitored in the LHCII trimers and aggregates. Global analysis of the two-dimensional (2D) spectra reveals that energy transfer from Chl b to Chl a occurs on fast and slow time scales of 240–270 fs and 2.8 ps for both forms of LHCII. 2D decay-associated spectra resulting from the global analysis identify the correlation between Chl states involved in the energy transfer and decay at a given lifetime. The contribution of singlet–singlet annihilation on the kinetics of Chl energy transfer and decay is also modelled and discussed. The results show a marked change in the energy transfer kinetics in the time range of a few picoseconds. Owing to slow energy equilibration processes, long-lived intermediate Chl a states are present in solubilized trimers, while in aggregates, the population decay of these excited states is significantly accelerated, suggesting that, overall, the energy transfer within the LHCII complexes is faster in the aggregated state.||URI:||https://hdl.handle.net/10356/97312
|ISSN:||0021-9606||DOI:||10.1063/1.4919239||Rights:||© 2015 AIP Publishing LLC. This paper was published in Journal of Chemical Physics and is made available as an electronic reprint (preprint) with permission of AIP Publishing LLC. The paper can be found at the following official DOI: [http://dx.doi.org/10.1063/1.4919239]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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