Atomic Scale Insights into the Early Stages of Metal Oxidation: A Scanning Tunneling Microscopy and Spectroscopy Study of Cobalt Oxidation

被引:12
|
作者
Picone, A. [1 ]
Riva, M. [1 ,2 ]
Brambilla, A. [1 ]
Giannotti, D. [1 ]
Ivashko, O. [1 ,3 ]
Bussetti, G. [1 ]
Finazzi, M. [1 ]
Ciccacci, F. [1 ]
Duo, L. [1 ]
机构
[1] Politecn Milan, Dipartimento Fis, Piazza Leonardo do Vinci 32, I-20133 Milan, Italy
[2] TU Wien, Inst Appl Phys, Wiedner Hauptstr 8-10, A-1040 Vienna, Austria
[3] Univ Zurich, Inst Phys, Winterthurerstr 190, CH-8057 Zurich, Switzerland
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2016年 / 120卷 / 09期
关键词
INITIAL OXIDATION; ULTRATHIN FILMS; WORK FUNCTION; OXIDE-GROWTH; 001; SURFACE; OXYGEN; FE(001); NI; NANOSCALE; COO;
D O I
10.1021/acs.jpcc.6b00384
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
Understanding the mechanisms driving the early stages of oxidation of metallic surfaces is of fundamental importance in fields such as nanocatalysis, electrochemistry, and nanoelectronics. In this work, the early, stages of oxidation of ultrathin Co films deposited on the Fe(001)-p(1 x 1)O surface have been investigated by means of Auger electron spectroscopy, scanning tunneling microscopy, and scanning tunneling spectroscopy. The oxidation is initiated by homogeneous oxide nucleation over the atomically flat Co terraces, inducing the development of a smooth oxide wetting layer when the islands coalesce. Atomically resolved images reveal that the oxide wetting layer is highly defective, possibly due to the presence of oxygen vacancies. Constant current scanning tunneling microscopy images acquired in different tunneling conditions, as well as scanning tunneling spectroscopy, reveal the distinct electronic properties of the oxide nuclei with respect to the chemisorbed phase. The fundamental band gap develops since the early stages of oxide nucleation. Moreover, spectroscopic curves acquired in the near-field-emission regime reveal a significant lowering of the sample work function induced by the oxide development. Our results represent a remarkable case in which metal oxidation can be studied at the atomic-scale level.
引用
收藏
页码:5233 / 5241
页数:9
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