Photoinduced Electron Transfer in a BODIPY-ortho-Carborane Dyad Investigated by Time-Resolved Transient Absorption Spectroscopy

2018 ◽  
Vol 122 (13) ◽  
pp. 3391-3397 ◽  
Author(s):  
So-Yoen Kim ◽  
Yang-Jin Cho ◽  
Ho-Jin Son ◽  
Dae Won Cho ◽  
Sang Ook Kang
Keyword(s):  
Electron Transfer ◽  
Absorption Spectroscopy ◽  
Photoinduced Electron Transfer ◽  
Transient Absorption ◽  
Transient Absorption Spectroscopy ◽  
Time Resolved

scholarly journals Interaction of light with a non-covalent zinc porphyrin–graphene oxide nanohybrid

2020 ◽  
Vol 22 (24) ◽  
pp. 13456-13466
Author(s):  
Ewelina Gacka ◽  
Gotard Burdzinski ◽  
Bronisław Marciniak ◽  
Adam Kubas ◽  
Anna Lewandowska-Andralojc
Keyword(s):  
Electron Transfer ◽  
Graphene Oxide ◽  
Absorption Spectroscopy ◽  
Fast Electron ◽  
Transient Absorption ◽  
Singlet State ◽  
Transient Absorption Spectroscopy ◽  
Time Resolved ◽  
Zinc Porphyrin

Fast electron transfer from the photoexcited ZnTPPH singlet state to GO sheets was detected by ultrafast time-resolved transient absorption spectroscopy.

Roles of adsorption sites in electron transfer from CdS quantum dots to molecular catalyst cobaloxime studied by time-resolved spectroscopy

2016 ◽  
Vol 18 (26) ◽  
pp. 17389-17397 ◽  
Author(s):  
Yun Ye ◽  
Yuxing Xu ◽  
Lei Huang ◽  
Dayong Fan ◽  
Zhaochi Feng ◽  
...  
Keyword(s):  
Quantum Dots ◽  
Electron Transfer ◽  
Absorption Spectroscopy ◽  
Transient Absorption ◽  
Transient Absorption Spectroscopy ◽  
Cds Quantum Dots ◽  
Time Resolved ◽  
Time Resolved Spectroscopy ◽  
Molecular Catalyst ◽  
Adsorption Sites

Electron transfer from CdS quantum dots (QDs) to cobaloxime (Co(dmgH)2pyCl) is demonstrated by transient absorption spectroscopy (TAS), and further confirmed using photoluminescence (PL) techniques.

Photoinduced electron transfer (PET) versus excimer formation in supramolecular p/n-heterojunctions of perylene bisimide dyes and implications for organic photovoltaics

2015 ◽  
Vol 185 ◽  
pp. 507-527 ◽  
Author(s):  
Agnieszka Nowak-Król ◽  
Benjamin Fimmel ◽  
Minjung Son ◽  
Dongho Kim ◽  
Frank Würthner
Keyword(s):  
Electron Transfer ◽  
Organic Solar Cells ◽  
Photoinduced Electron Transfer ◽  
Transient Absorption ◽  
Model Systems ◽  
Transient Absorption Spectroscopy ◽  
Time Resolved ◽  
Perylene Bisimide ◽  
Excimer Formation ◽  
Molecular Semiconductor

Foldamer systems comprised of two perylene bisimide (PBI) dyes attached to the conjugated backbones of 1,2-bis(phenylethynyl)benzene and phenylethynyl-bis(phenylene)indane, respectively, were synthesized and investigated with regard to their solvent-dependent properties. UV/Vis absorption and steady-state fluorescence spectra show that both foldamers exist predominantly in a folded H-aggregated state consisting of π–π-stacked PBIs in THF and in more random conformations with weaker excitonic coupling between the PBIs in chloroform. Time-resolved fluorescence spectroscopy and transient absorption spectroscopy reveal entirely different relaxation pathways for the photoexcited molecules in the given solvents, i.e. photoinduced electron transfer leading to charge separated states for the open conformations (in chloroform) and relaxation into excimer states with red-shifted emission for the stacked conformations (in THF). Supported by redox data from cyclic voltammetry and Rehm–Weller analysis we could relate the processes occurring in these solution-phase model systems to the elementary processes in organic solar cells. Accordingly, only if relaxation pathways such as excimer formation are strictly avoided in molecular semiconductor materials, excitons may diffuse over larger distances to the heterojunction interface and produce photocurrent via the formation of electron/hole pairs by photoinduced electron transfer.

Intramolecular electron transfer reactions in meso-(4-nitrophenyl)-substituted subporphyrins

2016 ◽  
Vol 52 (7) ◽  
pp. 1424-1427 ◽  
Author(s):  
Graeme Copley ◽  
Juwon Oh ◽  
Kota Yoshida ◽  
Daiki Shimizu ◽  
Dongho Kim ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Absorption Spectroscopy ◽  
Charge Separation ◽  
Transient Absorption ◽  
Charge Recombination ◽  
Transient Absorption Spectroscopy ◽  
Transfer Reactions ◽  
Intramolecular Electron Transfer ◽  
Time Resolved ◽  
Electron Transfer Reactions

A2B-type meso-(4-nitrophenyl)-substituted subporphyrins have been synthesized and shown to undergo very fast photoinduced intramolecular charge separation (CS) and charge recombination (CR) between the subporphyrin core and the meso-4-nitrophenyl group in CH2Cl2 as probed by femtosecond time-resolved transient absorption spectroscopy.

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