期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 121, 期 12, 页码 6701-6711出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b12803
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资金
- Science Foundation Ireland [SFI 15/ERC-13142]
We have investigated static/structural as well as dynamical properties of anatase (101) and rutile (110) TiO2 interfaces with liquid bulk water by reactive force fields (ReaxFF). Layered, well-organized structure of water in the interface region was clearly observed within 6.5 angstrom of the surfaces. The first-hydration layer molecules adsorbed to unsaturated surface Ti atoms undergo spontaneous dissociation leading, rather controversially, to full coverage of O-2/O-b by H+ and partial coverage of Ti-sc by OH-. Expected large variations of intrinsic electric field on the interfaces, and drop of electrostatic potential, were detected. Interfacial water was found to be heavily confined with a self-diffusion constant of 2 orders of magnitude lower than 2.28 X 10(-9) m(2)/s measured in the bulk water region. Moreover, the rotational movement of adsorbed water molecules was found to be considerably hindered as well. On the other hand, the calculated hydrogen-bond lifetime on the interface was shorter than in bulk water for both surface types. Finally, the IR spectra obtained from collective-water-dipole variations in the interfacial region revealed stronger effects on stretching vibrations on anatase (101) than on ruffle (110); however, description of liquid-water bond-stretching vibrations generally suffers from lack of accuracy in the applied reactive potential.
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