期刊
JOURNAL OF PHYSICAL CHEMISTRY B
卷 125, 期 16, 页码 3977-3985出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.0c11024
关键词
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资金
- DAE (HBNI, BARC)
The study reveals that the perturbation of interfacial water by kosmotropic electrolytes causes a stronger hydrogen bond formation with surface-expelled anions, resulting in a more heterogeneous interface.
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 (Na2CO3 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 (CO32- 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.
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