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  4. Photexcitation of Aqueous Ruthenium(II)-tris-(2,2'-bipyridine) with High-Intensity Femtosecond Laser Pulses
 
research article

Photexcitation of Aqueous Ruthenium(II)-tris-(2,2'-bipyridine) with High-Intensity Femtosecond Laser Pulses

Tarnovsky, A. N.
•
Gawelda, W.  
•
Johnson, M.
Show more
2006
The Journal of Physical Chemistry B

The authors report a femtosecond pump-probe study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+, as a function of pump power (up to 2 TW/cm2) at 400 nm excitation. The transient absorption spectra in the 345-660 nm range up to 1 ns time delay enable the observation of the following photoproducts: the triplet 3MLCT (metal-to-ligand-charge-transfer) excited state, the reduced form [Ru(bpy)3]+, the oxidized species [Ru(bpy)3]3+, and the solvated electron eaq. The 3MLCT state is formed within the excitation pulse and undergoes vibrational relaxation in 3-5 ps, as evidenced by the shift of the ligand-centered (LC) absorption band below 400 nm. Even at the highest pump powers, the majority of eaq originates from multiphoton ionization of [RuII(bpy)3]2+ and not from the solvent, generating [RuIII(bpy)3]3+ as a byproduct. At 10 ps time delay, the total concn. of the three product species is balanced by the depleted concn. of [RuII(bpy)3]2+, even at the highest fluences used, indicating that no further reaction products significantly contribute to the overall photochem. On the 100 ps time scale, most probably diffusion-controlled redn. of ground-state [RuII(bpy)3]2+ by solvated electrons occurs, next to recombination between eaq and [RuIII(bpy)3]3+. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1021/jp064696f
Web of Science ID

WOS:000242974300129

Author(s)
Tarnovsky, A. N.
Gawelda, W.  
Johnson, M.
Bressler, C.  
Chergui, M.  
Date Issued

2006

Published in
The Journal of Physical Chemistry B
Volume

110

Issue

51

Start page

26497

End page

26505

Subjects

Excited triplet state (MLCT; transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); Photoionization (multiphoton; transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); Redox reaction (photoredox; transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); Laser radiation (pulsed; transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); Intersystem crossing; Solvated electrons; Vibrational relaxation (transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); Optical absorption (transient; transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); Charge transfer state (triplet metal-to-ligand; transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation)

•

photolysis bipyridine ruthenium complex intense laser pulse solvated electron; triplet charge transfer state photolysis bipyridine ruthenium complex; transient absorption photochem bipyridine ruthenium complex intense femtosecond excitation

Note

CAN 146:216201

74-1

Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes

Laboratory of Ultrafast Spectroscopy, ISIC, BSP,Ecole Polytechnique Federale de Lausanne,Lausanne-Dorigny,Switz.

Journal

written in English.

18955-01-6 (Tris(2,2'-bipyridine)ruthenium(3+); 56977-24-3 (Tris(2,2'-bipyridine)ruthenium(1+) Role: FMU (Formation, unclassified), PEP (Physical, engineering or chemical process), FORM (Formation, nonpreparative), PROC (Process) (transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation); 15158-62-0 (Tris(2,2'-bipyridine)ruthenium(2+) Role: PEP (Physical, engineering or chemical process), PRP (Properties), RCT (Reactant), PROC (Process), RACT (Reactant or reagent) (transient absorption study of photochem. of concd. aq. solns. of [Ru(bpy)3]2+ under high-intensity femtosecond laser excitation)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSU  
Available on Infoscience
May 31, 2007
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/7505
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