Structure and charging of hydrophobic material/water interfaces studied by phase-sensitive sum-frequency vibrational spectroscopy

被引:264
作者
Tian, C. S. [1 ]
Shen, Y. R. [1 ]
机构
[1] Univ Calif Berkeley, Dept Phys, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
surface charging; octadecyltrichlorosilane; hydronium; hydroxide; SELF-ASSEMBLED MONOLAYERS; MOLECULAR-DYNAMICS; AQUEOUS-SOLUTIONS; WATER-STRUCTURE; HYDROXIDE IONS; LIQUID WATER; SURFACE; ADSORPTION; HYDROGEN; GAS;
D O I
10.1073/pnas.0901480106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have studied the hydrophobic water/octadecyltrichlorosilane (OTS) interface by using the phase-sensitive sum-frequency vibrational spectroscopy (PS-SFVS), and we obtained detailed structural information of the interface at the molecular level. Excess ions emerging at the interface were detected by changes of the surface vibrational spectrum induced by the surface field created by the excess ions. Both hydronium (H3O+) and hydroxide (OH-) ions were found to adsorb at the interface, and so did other negative ions such as Cl-. By varying the ion concentrations in the bulk water, their adsorption isotherms were measured. It was seen that among the three, OH-has the highest adsorption energy, and H3O+ has the lowest; OH-also has the highest saturation coverage, and Cl-has the lowest. The result shows that even the neat water/OTS interface is not neutral, but charged with OH-ions. The result also explains the surprising observation that the isoelectric point appeared at similar to 3.0 when HCl was used to decrease the pH starting from neat water.
引用
收藏
页码:15148 / 15153
页数:6
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