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Ultrafast transient-absorption spectroscopy of the aqueous solvated electron
We have performed the first direct pump-probe transient-absorption measurements on the near-infrared (IR) band of the equilibrated aqueous solvated electron. The pump pulse was centered at 780 nm. The absorption spectrum of the excited state is observed to be red-shifted relative to the ground-state...
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Published in: | The Journal of chemical physics 1993-04, Vol.98 (7), p.5996-5998 |
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container_end_page | 5998 |
container_issue | 7 |
container_start_page | 5996 |
container_title | The Journal of chemical physics |
container_volume | 98 |
creator | ALFANO, J. C WALHOUT, P. K KIMURA, Y BARBARA, P. F |
description | We have performed the first direct pump-probe transient-absorption measurements on the near-infrared (IR) band of the equilibrated aqueous solvated electron. The pump pulse was centered at 780 nm. The absorption spectrum of the excited state is observed to be red-shifted relative to the ground-state absorption. The radiationless transition from the excited state to the ground state occurs with an average time constant of 550±170 fs. In observing a subpicosecond lifetime and red-shifted absorption for the excited p-states, these experiments are in accord with a growing body of experimental and theoretical work, serving to provide a consistent picture of the photophysics of the solvated electron. |
doi_str_mv | 10.1063/1.464839 |
format | article |
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C ; WALHOUT, P. K ; KIMURA, Y ; BARBARA, P. F</creator><creatorcontrib>ALFANO, J. C ; WALHOUT, P. K ; KIMURA, Y ; BARBARA, P. F</creatorcontrib><description>We have performed the first direct pump-probe transient-absorption measurements on the near-infrared (IR) band of the equilibrated aqueous solvated electron. The pump pulse was centered at 780 nm. The absorption spectrum of the excited state is observed to be red-shifted relative to the ground-state absorption. The radiationless transition from the excited state to the ground state occurs with an average time constant of 550±170 fs. 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The absorption spectrum of the excited state is observed to be red-shifted relative to the ground-state absorption. The radiationless transition from the excited state to the ground state occurs with an average time constant of 550±170 fs. In observing a subpicosecond lifetime and red-shifted absorption for the excited p-states, these experiments are in accord with a growing body of experimental and theoretical work, serving to provide a consistent picture of the photophysics of the solvated electron.</abstract><cop>Woodbury, NY</cop><pub>American Institute of Physics</pub><doi>10.1063/1.464839</doi><tpages>3</tpages></addata></record> |
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source | American Institute of Physics (AIP) Publications |
subjects | Chemistry Exact sciences and technology General and physical chemistry Physical chemistry of induced reactions (with radiations, particles and ultrasonics) Q1 Solvated and trapped electrons Water |
title | Ultrafast transient-absorption spectroscopy of the aqueous solvated electron |
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