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- W2947840488 abstract "Two-dimensional (2D) nanostructures are an emerging class of materials for designing artificial light-harvesting system because of their unprecedented electronic properties. Here, we design 2D nanoassembly of 5,10,15,20-tetra(4-dodecyloxyphenyl) porphyrin by changing solvent polarity. We provide molecular dynamics simulation data to understand the internal structure of the 2D porphyrin nanostructures and study their exciton dynamics by femtosecond transient absorption spectroscopy. We find that porphyrins incline to stack on each other in parallel-displaced manner, which results in the formation of right-handed helix within the nanoassembly. Long alkyl side chains tightly wrap around each other to reduce the hydrophobic solvent-accessible surface area, which results in the formation of 2D nanodisk structure where the central porphyrin moieties exist as disjoined helices. Ultrafast spectroscopic study of 2D porphyrin aggregate exhibits very fast internal conversion process from S2 → S1 transition in ∼100 fs time scale along with direct S2 → S0 transition in 350 fs. The vibrational cooling and relaxation process (inside S1 manifold) is found to be decreased from 10 ps (monomer) to 5 ps (aggregated structure). It is evident that the probability of intersystem crossing from S1 (or S2) to T1 state is greatly reduced due to aggregation. Analysis reveals that the fabrication of 2D porphyrin structures and study of excited-state dynamics would be paved in designing and mimicking the organic-based artificial light-harvesting system." @default.
- W2947840488 created "2019-06-07" @default.
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- W2947840488 date "2019-05-30" @default.
- W2947840488 modified "2023-10-16" @default.
- W2947840488 title "Structural Insight and Ultrafast Dynamics of 2D Porphyrin Nanostructures" @default.
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- W2947840488 doi "https://doi.org/10.1021/acs.jpcc.9b03112" @default.
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