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Formation and splitting of paired hydroxyl groups on reduced TiO2(110) - art. no. 066107
被引:380
作者:

Wendt, S
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Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark

Matthiesen, J
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机构: Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark

Schaub, R
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机构: Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark

Vestergaard, EK
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机构: Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark

Lægsgaard, E
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机构: Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark

Besenbacher, F
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机构: Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark

Hammer, B
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机构: Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark
机构:
[1] Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark
[2] Univ Aarhus, Dept Phys & Astron, DK-8000 Aarhus C, Denmark
关键词:
D O I:
10.1103/PhysRevLett.96.066107
中图分类号:
O4 [物理学];
学科分类号:
0702 ;
摘要:
A combination of high-resolution scanning tunneling microscopy and density functional theory is utilized to study the interaction of water with the reduced TiO2(110)-(1x1) surface. As the direct product of water dissociation in oxygen vacancies, paired hydroxyl groups are formed. These pairs are immobile and stable unless they interact with adsorbed water molecules. As a result of these interactions, protons are transferred to adjacent oxygen rows, thereby forming single hydroxyl groups. Additionally, we show that hydroxyl groups facilitate the diffusion of water molecules over the oxygen rows.
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