Time Resolved Holography For Investi Gation Of Yag :Er Laser (λ=2.94µ) - Liquid Water Interaction

Author(s):  
A. V. Lukashev ◽  
K. L. Vodopyanov ◽  
L. A. Kulevsky ◽  
A. V. Lukashev ◽  
K. L. Vodopyanov ◽  
...  
2007 ◽  
Vol 126 (3) ◽  
pp. 034511 ◽  
Author(s):  
Wafa Amir ◽  
Guilhem Gallot ◽  
François Hache ◽  
S. Bratos ◽  
J.-C. Leicknam ◽  
...  
Keyword(s):  

2009 ◽  
Vol 96 (1) ◽  
pp. 11-18 ◽  
Author(s):  
G. Gavrila ◽  
K. Godehusen ◽  
C. Weniger ◽  
E. T. J. Nibbering ◽  
T. Elsaesser ◽  
...  

Science ◽  
2020 ◽  
Vol 369 (6506) ◽  
pp. 974-979
Author(s):  
Inga Jordan ◽  
Martin Huppert ◽  
Dominik Rattenbacher ◽  
Michael Peper ◽  
Denis Jelovina ◽  
...  

Electronic dynamics in liquids are of fundamental importance, but time-resolved experiments have so far remained limited to the femtosecond time scale. We report the extension of attosecond spectroscopy to the liquid phase. We measured time delays of 50 to 70 attoseconds between the photoemission from liquid water and that from gaseous water at photon energies of 21.7 to 31.0 electron volts. These photoemission delays can be decomposed into a photoionization delay sensitive to the local environment and a delay originating from electron transport. In our experiments, the latter contribution is shown to be negligible. By referencing liquid water to gaseous water, we isolated the effect of solvation on the attosecond photoionization dynamics of water molecules. Our methods define an approach to separating bound and unbound electron dynamics from the structural response of the solvent.


RSC Advances ◽  
2017 ◽  
Vol 7 (13) ◽  
pp. 7610-7618 ◽  
Author(s):  
Hiroyuki Okamura ◽  
Noboru Aoyagi ◽  
Kojiro Shimojo ◽  
Hirochika Naganawa ◽  
Hisanori Imura

The replacement of water molecules of [Eu(tta)3(H2O)3] with Tf2N− was evidenced in water-saturated [Cnmim][Tf2N] by time-resolved laser-induced fluorescence spectroscopy.


2018 ◽  
Vol 75 (4) ◽  
pp. 1045-1062 ◽  
Author(s):  
M. Pinsky ◽  
A. Khain ◽  
A. Korolev

Abstract The process of ice–liquid water interaction in the unsaturated environment is explored both analytically and with the help of a numerical simulation. Ice–liquid water interaction via the condensation–evaporation mechanism is considered in relation to the problem of homogeneous mixing in an unmovable air volume. The process is separated into three stages: the homogenization stage, during which the rapid alignment of thermodynamic and microphysical parameters in the mixing volume takes place; the glaciation stage, during which the liquid droplets evaporate; and the ice stage, which leads to attaining a thermodynamic equilibrium. Depending on the initial temperature, humidity, and mixing ratios of liquid water and of ice water, the third stage may result in two outcomes: existence of ice particles under zero supersaturation with respect to ice or a complete disappearance of ice particles. Three characteristic times are associated with the microphysical stages: the phase relaxation time associated with droplets, the glaciation time determined by the Wegener–Bergeron–Findeisen process, and the phase relaxation time associated with ice. Since the duration of the second and third microphysical stages may be of the same order as the homogenization time or even longer, the homogeneous mixing scenario is more probable in mixed-phase clouds than in liquid clouds. It is shown that mixing of a mixed-phase cloud with a dry environment accelerates cloud glaciation, leading to a decrease in the glaciation time by more than 2 times. The conditions of fast ice particles’ disappearance due to sublimation are analyzed as well.


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