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

被引:29
|
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
来源
JOURNAL OF CHEMICAL PHYSICS | 2014年 / 141卷 / 21期
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
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页数:9
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