Water Dynamics at the Interface in AOT Reverse Micelles

被引:112
作者
Moilanen, David E. [1 ]
Fenn, Emily E. [1 ]
Wong, Daryl [1 ]
Fayer, M. D. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ECHO CORRELATION SPECTROSCOPY; LIQUID WATER; HYDRATION DYNAMICS; HYDROGEN-BONDS; CONFINED WATER; REORIENTATION; RELAXATION; MOLECULES; MECHANISM; SULFOSUCCINATE;
D O I
10.1021/jp902004r
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
The orientational dynamics of water molecules at the interface in large Aerosol-OT (AOT) reverse micelles are investigated using ultrafast infrared spectroscopy of the OD stretch of dilute HOD in H2O. In large reverse micelles (similar to 9 nm diameter or larger), a significant amount of the nanoscopic water is sufficiently distant from the interface that it displays bulk-like characteristics. However, some water molecules interact with the interface and have vibrational absorption spectra and dynamics distinct from bulk water. The different characteristics of these interfacial waters allow their contribution to the data to be separated from the bulk. The infrared absorption spectrum of the OD stretch is analyzed to show that the interfacial water molecules have a spectrum that peaks near 2565 cm(-1) in contrast to 2509 cm(-1) in bulk water. A two-component model is developed that simultaneously describes the population relaxation and orientational dynamics of the OD stretch in the spectral region of the interfacial water. The model provides a consistent description of both observables and demonstrates that water interacting with the interface has slower vibrational relaxation and orientational dynamics. The orientational relaxation of interfacial water molecules occurs in 18 +/- 3 ps, in contrast to the bulk water value of 2.6 ps.
引用
收藏
页码:8560 / 8568
页数:9
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