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Interfacial Electron Transfer Dynamics of Two Newly Synthesized Catecholate Bound Ru II Polypyridyl‐Based Sensitizers on TiO 2 Nanoparticle Surface – A Femtosecond Pump Probe Spectroscopic Study
Author(s) -
Banerjee Tanmay,
Rawalekar Sachin,
Das Amitava,
Ghosh Hirendra N.
Publication year - 2011
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201100411
Subject(s) - chemistry , ruthenium , ultrafast laser spectroscopy , photochemistry , electron transfer , bipyridine , hexafluorophosphate , absorption spectroscopy , nanoparticle , spectroscopy , crystallography , organic chemistry , catalysis , nanotechnology , materials science , physics , ionic liquid , quantum mechanics , crystal structure
Two new catecholate‐bound Ru II –polypyridine based sensitizers, (2,2′‐bipyridine){ethyl 3‐(4‐hydroxyphenyl)‐2‐[(4′‐methyl‐2,2′‐bipyridinyl‐4‐carbonyl)amino]propionate}{4‐[2‐(4′‐methyl‐2,2′‐bipyridinyl‐4‐yl)vinyl]benzene‐1,2‐diol)}ruthenium(II) hexafluorophosphate ( 5 ) and [(2,2′‐bipyridine)‐(4‐2,2′‐bipyridinyl‐4‐yl‐phenol)‐(4‐{2‐(4′‐methyl‐2,2′‐bipyridinyl‐4‐yl)vinyl}benzene‐1,2‐diol)]ruthenium(II) hexafluorophosphate ( 6 ) with secondary electron‐donating groups (tyrosine and phenol, respectively) were synthesized and characterized. Steady‐state optical absorption and emission studies confirm strong coupling between the sensitizers and TiO 2 nanoparticles. Femtosecond visible transient absorption spectroscopy has been employed to study interfacial electron transfer (IET) dynamics in the dye–nanoparticle systems to explore the influence of the secondary electron‐donating groups on IET dynamics. Electron injection into the conduction band of nanoparticulate TiO 2 has been confirmed by detection of the conduction band electrons in TiO 2 ([e – ] TiO2 CB ) and radical cation of the adsorbed dye (D · + ) in real time monitored by transient absorption spectroscopy. A single exponential and pulse‐width limited (< 100 fs) electron injection has been observed. Back electron transfer (BET) dynamics have been studied by monitoring the decay kinetics of the injected electron in the conduction band of TiO 2 and by the recovery of the ground state bleach. BET dynamics in dye–TiO 2 systems for complexes 5 and 6 have been compared with those of [bis(2,2′‐bpy)‐(4‐{2‐(4′‐methyl‐2,2′‐bipyridinyl‐4‐yl)vinyl}benzene‐1,2‐diol)]ruthenium(II) hexafluorophosphate ( 7 ), which does not have a secondary electron‐donating group.