Nucleation and growth of Pt nanoparticles on reduced and oxidized rutile TiO2 (110)

被引:30
作者
Rieboldt, F. [1 ]
Vilhelmsen, L. B. [1 ]
Koust, S. [1 ]
Lauritsen, J. V. [1 ]
Helveg, S. [2 ]
Lammich, L. [1 ]
Besenbacher, F. [1 ]
Hammer, B. [1 ]
Wendt, S. [1 ]
机构
[1] Aarhus Univ, Dept Phys & Astron, Interdisciplinaly Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[2] Haldor Topsoe Res Labs, DK-2800 Lyngby, Denmark
基金
欧洲研究理事会;
关键词
REDUCTION STATE; SURFACE SCIENCE; OXIDE SURFACES; OXYGEN; TIO2(110); OXIDATION; ADSORPTION; RESOLUTION; CATALYSTS; CLUSTERS;
D O I
10.1063/1.4902249
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The nucleation and growth of Pt nanoparticles (NP's) on rutile TiO2 (110) surfaces with O on-top atoms (oxidized TiO2), surface O vacancies, and H adatoms, respectively (reduced TiO2), was studied by means of scanning tunneling microscopy (STM) experiments and density functional theory calculations. At room temperature, Pt was found to be trapped at O on-top atoms and surface O vacancies, leading to rather small Pt NP's. In contrast, on surfaces with H adatoms the mobility of Pt was much larger. As a result, large Pt NP's were found at room temperature on TiO2 (110) surfaces with H adatoms. However, at similar to 150 K the diffusion of Pt was kinetically hindered on all TiO2 (110) surfaces considered. STM data acquired after vacuum-annealing at 800 K showed comparable results on all TiO2 (110) surfaces because the diffusion of Pt is not influenced by surface defects at such high temperatures. (C) 2014 AIP Publishing LLC.
引用
收藏
页数:9
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