Aqueous solvation dynamics at metal oxide surfaces

被引:6
作者
Portuondo-Campa, E
Tortschanoff, A [1 ]
van Mourik, F
Moser, JE
Kornherr, A
Chergui, M
机构
[1] Ecole Polytech Fed Lausanne, ISIC, Lab Spectroscopie Ultrarapide, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, ISIC, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[3] Univ Vienna, Inst Phys Chem, A-1090 Vienna, Austria
关键词
D O I
10.1021/jp056442k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Broadband transient absorption (TA) spectroscopy, three-pulse photon echo peak shift (3PEPS), and anisotropy decay measurements were used to study the solvation dynamics in bulk water and interfacial water at ZrO2 surfaces, using Eosin Y as a probe. The 3PEPS results show a multiexponential behavior with two subpicosecond components that are similar in bulk and interfacial water, while a third component of several picoseconds is significantly lengthened at the interface. The bandwidth correlation function from TA spectra exhibits the same behavior, and the TA spectra are well reproduced using the doorway-window picture with the time constants from PEPS. Our results suggest that interfacial water is restricted to a thickness of less than 5 angstrom. Also the high-frequency collective dynamics of water does not seem to be affected by the interface. On the other hand, the increase of the third component may point to a slowing down of diffusional motion at the interface, although other effects, may play a role, which are discussed.
引用
收藏
页码:7835 / 7844
页数:10
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