Roy Subhadip, Mondal Jahur Alam
Radiation & Photochemistry Division, Bhabha Atomic Research Centre, Homi Bhabha National Institute, Trombay, Trombay, Mumbai 400085, India.
J Phys Chem B. 2021 Apr 29;125(16):3977-3985. doi: 10.1021/acs.jpcb.0c11024. Epub 2021 Apr 20.
The ion-driven electric double layer (EDL) and the structural transformation of interfacial water are implicated in unusual reaction kinetics at the air/water interface. By combining heterodyne-detected vibrational sum frequency generation (HD-VSFG) with differential spectroscopy involving simultaneous curve fitting (DS-SCF) analysis, we retrieve electrolyte (NaCO and NaF)-correlated OH-stretch spectra of water at the air/water interface. Vibrational mapping of the perturbed interfacial water with the hydration shell spectra (obtained by DS-SCF analysis of Raman spectra) of the corresponding anion discloses that the kosmotropic electrolytes do not form well-defined EDL at the air/water interface. Instead, the interfacial water forms a stronger hydrogen-bond with the surface-expelled anions (CO and F) and becomes more inhomogeneous than the pristine air/water interface. Together, the results reveal that the perturbation of interfacial water by the kosmotropic electrolyte is a "local phenomenon" confined within the hydration shell of the surface-expelled anion.
离子驱动的双电层(EDL)和界面水的结构转变与气/水界面处异常的反应动力学有关。通过将外差检测振动和频产生(HD-VSFG)与涉及同步曲线拟合(DS-SCF)分析的差分光谱相结合,我们获取了气/水界面处与电解质(NaCO和NaF)相关的水的OH伸缩光谱。用相应阴离子的水合壳层光谱(通过拉曼光谱的DS-SCF分析获得)对受扰动的界面水进行振动映射,结果表明,促离子型电解质在气/水界面处不会形成明确的双电层。相反,界面水与表面排出的阴离子(CO和F)形成更强的氢键,并且比原始气/水界面更加不均匀。总之,结果表明促离子型电解质对界面水的扰动是一种“局部现象”,局限于表面排出阴离子的水合壳层内。