| Literature DB >> 18654687 |
Chun-Rong Wang1, Ting Luo, Qing-Bin Lu.
Abstract
Despite intense study over the past two decades, the dynamics of electron solvation in water, particularly regarding the physical properties and lifetimes of non-equilibrium, incompletely relaxed electrons, remain very controversial. Both experimental and theoretical studies have reported a very diverse range, from approximately 50 to approximately 1000 fs, for the lifetime of the p-like excited state of the hydrated electron, and the nature of incompletely relaxed states remains unclear. Here, we reveal that these controversies are to a great extent due to a hidden effect, i.e., the universal existence of a coherence spike at delay time zero in pump-probe spectroscopic kinetics traces. After removing this spike effect, we show that the intrinsic lifetimes of the two incompletely relaxed states in bulk water are 180+/-30 and 545+/-30 fs, respectively. Moreover, our results using iododeoxyuridine as a molecular probe reveal that both states are electronically excited states of the hydrated electron and the second state of a 545 fs lifetime is the long-sought wet electron. These results resolve the long-standing controversies about electron hydration dynamics.Entities:
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Year: 2008 PMID: 18654687 DOI: 10.1039/b806287k
Source DB: PubMed Journal: Phys Chem Chem Phys ISSN: 1463-9076 Impact factor: 3.676