期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 113, 期 17, 页码 7236-7245出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp809596q
关键词
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资金
- Grant-in-Aid for Scientific Research on Priority Area [20027002, 20038017]
- Ministry of Education, Culture, Sports, Science, and Technology of Japan
- Grants-in-Aid for Scientific Research [20613002, 20038017, 20027002] Funding Source: KAKEN
Heterogeneous electron transfer dynamics at molecule-metal or molecule-metal oxide interfaces are a central issue for many fields in surface science. Recent time-resolved two-photon photoemission studies observed electron solvation at protic molecule-metal or -metal oxide interfaces in photoinduced charge transfer processes. Although the solvated electron is expected as a functional state (for instance, highly catalytic active site, promoter of charge transfer at devices), details are not yet well understood because of the strong dependence of specific atomistic-level solvent-substrate interactions on interfaces, e.g., ordered hydrogen. bonds or defects at surfaces. We focus on the interfaces of H2O/TiO2(110) and CH3OH/TiO2(110) and have applied ab initio DFT calculations for several structures with changing coverage and adsorption types and after inserting oxygen vacancies. The electronic structures of wet-electron states and hydrogen bonds at interfaces have been analyzed using the calculated results.
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