Molecular Spectroscopy Laboratory, Advanced Science Institute (ASI), RIKEN, 2-1 Hirosawa, Wako 351-0198, Japan.
J Chem Phys. 2010 Apr 14;132(14):144701. doi: 10.1063/1.3372620.
A solute-solvent interaction at the air/water interface was investigated both experimentally and theoretically, by studying a prototypical surface-active polarity indicator molecule, coumarin 110 (C110), adsorbed at the air/water interface with heterodyne-detected electronic sum frequency generation (HD-ESFG) spectroscopy, polarization second harmonic generation (SHG), and a molecular dynamics (MD) simulation. The second-order nonlinear optical susceptibility (chi((2))) tensor elements of C110 at the air/water interface were determined experimentally by HD-ESFG and polarization SHG, and information on "intermediate" polarity sensed by C110 at the interface was obtained by HD-ESFG. An MD simulation and a time-dependent density functional theory calculation were used to theoretically evaluate the chi((2)) tensor elements, which were in good agreement with the experimental results of HD-ESFG and polarization SHG. The microscopic "half-hydration" structure around C110 at the water surface was visualized on the basis of the MD simulation data, with which we can intuitively understand the microscopic origin of the surface activity of C110 and the intermediate polarity sensed by C110 at the air/water interface.
在空气/水界面处的溶质-溶剂相互作用进行了实验和理论研究,通过研究原型表面活性极性指示剂分子香豆素 110(C110),用异频检测电子和频光谱(HD-ESFG)、偏振二次谐波产生(SHG)和分子动力学(MD)模拟来吸附在空气/水界面上。通过 HD-ESFG 和偏振 SHG 实验确定了 C110 在空气/水界面的二阶非线性光学系数张量元素,并通过 HD-ESFG 获得了 C110 在界面处感知的“中间”极性信息。MD 模拟和含时密度泛函理论计算用于理论评估 chi((2))张量元素,与 HD-ESFG 和偏振 SHG 的实验结果吻合良好。基于 MD 模拟数据,可视化了 C110 在水面上的微观“半水合”结构,这使我们可以直观地理解 C110 的表面活性和 C110 在空气/水界面处感知的中间极性的微观起源。