Probing the Mineral-Water Interface with Nonlinear Optical Spectroscopy

被引:67
|
作者
Backus, Ellen H. G. [1 ,2 ]
Schaefer, Jan [1 ]
Bonn, Mischa [1 ]
机构
[1] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[2] Univ Vienna, Dept Phys Chem, Wahringer Str 42, A-1090 Vienna, Austria
基金
欧洲研究理事会;
关键词
alumina; calcium fluoride; nonlinear optics; silica; vibrational spectroscopy; SUM-FREQUENCY GENERATION; HETEROGENEOUS ICE NUCLEATION; 2ND-HARMONIC GENERATION; VIBRATIONAL SPECTROSCOPY; SURFACE-CHARGE; MOLECULAR-STRUCTURE; SALT-SOLUTIONS; DYNAMICS; SPECTRA; PHASE;
D O I
10.1002/anie.202003085
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interaction between minerals and water is manifold and complex: the mineral surface can be (de)protonated by water, thereby changing its charge; mineral ions dissolved into the aqueous phase screen the surface charges. Both factors affect the interaction with water. Intrinsically molecular-level processes and interactions govern macroscopic phenomena, such as flow-induced dissolution, wetting, and charging. This realization is increasingly prompting molecular-level studies of mineral-water interfaces. Here, we provide an overview of recent developments in surface-specific nonlinear spectroscopy techniques such as sum frequency and second harmonic generation (SFG/SHG), which can provide information about the molecular arrangement of the first few layers of water molecules at the mineral surface. The results illustrate the subtleties of both chemical and physical interactions between water and the mineral as well as the critical role of mineral dissolution and other ions in solution for determining those interactions.
引用
收藏
页码:10482 / 10501
页数:20
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