Zhang Wen-kai, Zheng De-sheng, Xu Yan-yan, Bian Hong-tao, Guo Yuan, Wang Hong-fei
State Key Laboratory of Molecular Reaction Dynamics, Institute of Chemistry, The Chinese Academy of Sciences, Beijing 100080, China.
J Chem Phys. 2005 Dec 8;123(22):224713. doi: 10.1063/1.2136875.
It has been generally accepted that there are significant quadrupolar and bulk contributions to the second-harmonic generation (SHG) reflected from the neat air/water interface, as well as common liquid interfaces. Because there has been no general methodology to determine the quadrupolar and bulk contributions to the SHG signal from a liquid interface, this conclusion was reached based on the following two experimental phenomena: the breaking of the macroscopic Kleinman symmetry and the significant temperature dependence of the SHG signal from the neat air/water interface. However, because the sum frequency generation vibrational spectroscopy (SFG-VS) measurement of the neat air/water interface observed no apparent temperature dependence, the temperature dependence in the SHG measurement has been reexamined and proven to be an experimental artifact. Here we present a complete microscopic analysis of the susceptibility tensors of the air/water interface, and show that dipolar contribution alone can be used to address the issue of the breaking of the macroscopic Kleinman symmetry at the neat air/water interface. Using this analysis, the orientation of the water molecules at the interface can be obtained, and it is consistent with the measurement from SFG-VS. Therefore, the key rationales to conclude significantly quadrupolar and bulk contributions to the SHG signal of the neat air/water interface can no longer be considered as valid as before. This new understanding of the air/water interface can shed light on our understanding of the nonlinear optical responses from other molecular interfaces as well.
人们普遍认为,从纯净的空气/水界面以及常见的液体界面反射的二次谐波产生(SHG)中,存在显著的四极和体相贡献。由于一直没有通用的方法来确定液体界面SHG信号的四极和体相贡献,这一结论是基于以下两个实验现象得出的:宏观克莱曼对称性的破坏以及纯净空气/水界面SHG信号显著的温度依赖性。然而,由于对纯净空气/水界面的和频振动光谱(SFG-VS)测量未观察到明显的温度依赖性,因此对SHG测量中的温度依赖性进行了重新审视,并证明这是一种实验假象。在此,我们对空气/水界面的极化率张量进行了完整的微观分析,并表明仅偶极贡献就可以解决纯净空气/水界面宏观克莱曼对称性破坏的问题。通过这种分析,可以获得界面处水分子的取向,这与SFG-VS的测量结果一致。因此,认为纯净空气/水界面的SHG信号有显著四极和体相贡献的关键依据不再像以前那样被认为是有效的。对空气/水界面的这种新认识也有助于我们理解其他分子界面的非线性光学响应。