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Adsorption-Site-Dependent Electronic Structure of Catechol on the Anatase TiO2(101) Surface
被引:44
作者:
Li, Shao-Chun
[1
]
Losovyj, Yaroslav
[2
]
Diebold, Ulrike
[1
,3
]
机构:
[1] Tulane Univ, Dept Phys & Engn Phys, New Orleans, LA 70118 USA
[2] Louisiana State Univ, Ctr Adv Microstruct & Devices, Baton Rouge, LA 70806 USA
[3] Vienna Univ Technol, Inst Appl Phys, A-1040 Vienna, Austria
来源:
关键词:
TIO2;
DYNAMICS;
PHOTOCATALYSIS;
NANOPARTICLES;
WATER;
GAP;
D O I:
10.1021/la201553k
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The adsorption of catechol (1,2-benzendiol) on the anatase TiO2(101) surface was studied with synchrotron-based ultraviolet photoemission spectroscopy (UPS), X-ray photoemission spectroscopy (XPS), and scanning tunneling microscopy (STM). Catechol adsorbs with a unity sticking coefficient and the phenyl ring intact. STM reveals preferred nucleation at step edges and subsurface point defects, followed by ID growth and the formation of a 2 x 1 superstructure at full coverage. A gap state of similar to 1 eV above the valence band maximum is observed for dosages in excess of similar to 0.4 Langmuir, but such a state is absent for lower coverages. The formation of the band gap states thus correlates with the adsorption at regular lattice sites and the onset of self-assembled superstructures.
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页码:8600 / 8604
页数:5
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