Journal
PHYSICAL REVIEW LETTERS
Volume 110, Issue 14, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.110.146101
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Funding
- Danish Research Agency
- Strategic Research Council
- Villum Kahn Rasmussen Foundation
- Lundbeck Foundation
- Carlsberg Foundation
- Danish Center for Scientific Computing
- European Research Council through Advanced ERC grant
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The water-TiO2 interaction is of paramount importance for many processes occurring on TiO2, and the rutile TiO2(110)-(1 x 1) surface has often been considered as a test case. Yet, no consensus has been reached whether the well-studied surface O vacancies on the terraces are the only active sites for water dissociation on rutile TiO2(110)-(1 x 1), or whether another channel for the creation of H adatoms exists. Here we use high-resolution scanning tunneling microscopy and density functional theory calculations to tackle this long-standing question. Evidence is presented that a second water dissociation channel exists on the surfaces of vacuum-annealed TiO2(110) crystals that is associated with the < 1 (1) over bar1 > step edges. This second water dissociation channel can be suppressed by blocking of the < 1 (1) over bar1 > step edges using ethanol. DOI: 10.1103/PhysRevLett.110.146101
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