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Real-time observation of the charge transfer to solvent dynamics
被引:68
作者:
Messina, Fabrizio
[1
]
Braem, Olivier
[1
]
Cannizzo, Andrea
[1
,2
]
Chergui, Majed
[1
]
机构:
[1] Ecole Polytech Fed Lausanne, Lab Spect Ultrarapide, ISIC FSB, EPFL, CH-1015 Lausanne, Switzerland
[2] Univ Bern, Inst Appl Phys, CH-3012 Bern, Switzerland
关键词:
RESOLVED PHOTOELECTRON-SPECTROSCOPY;
SOLVATION DYNAMICS;
FEMTOSECOND FLUORESCENCE;
ELECTRONIC-STRUCTURE;
RELAXATION DYNAMICS;
ULTRAFAST DYNAMICS;
AQUEOUS CHLORIDE;
IODIDE;
WATER;
PHOTODETACHMENT;
D O I:
10.1038/ncomms3119
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Intermolecular electron-transfer reactions have a crucial role in biology, solution chemistry and electrochemistry. The first step of such reactions is the expulsion of the electron to the solvent, whose mechanism is determined by the structure and dynamical response of the latter. Here we visualize the electron transfer to water using ultrafast fluorescence spectroscopy with polychromatic detection from the ultraviolet to the visible region, upon photo-excitation of the so-called charge transfer to solvent states of aqueous iodide. The initial emission is short lived (similar to 60 fs) and it relaxes to a broad distribution of lower-energy charge transfer to solvent states upon rearrangement of the solvent cage. This distribution reflects the inhomogeneous character of the solvent cage around iodide. Electron ejection occurs from the relaxed charge transfer to solvent states with lifetimes of 100-400 fs that increase with decreasing emission energy.
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