Water dissociation on mixed Co-Fe oxide bilayer nanoislands on Au(111)

被引:7
|
作者
Sun, Zhaozong [1 ]
Rodriguez-Fernandez, Jonathan [1 ,2 ]
Lauritsen, Jeppe, V [1 ]
机构
[1] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[2] Univ Oviedo, Dept Phys, Oviedo 33007, Spain
关键词
Co oxide; Fe oxide; mixed oxides; water exposure; hydroxylation; scanning tunnelling microscopy (STM); x-ray photoelectron spectroscopy (XPS); OXYGEN-EVOLUTION ELECTROCATALYSTS; TRANSITION-METAL (OXY)HYDROXIDES; COBALT; IRON; OXIDATION; ULTRATHIN; FEO(111); FILMS; ADSORPTION; STABILITY;
D O I
10.1088/1361-648X/ac513a
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
We investigate the hydroxylation behaviour of mixed Co-Fe oxide nanoislands synthesized on a Au(111) surface under exposure to water vapour at vacuum conditions. The pure Co and Fe bilayer oxides both become hydroxylated by water exposure in vacuum conditions, albeit to a very different extent. It is however an open question how mixed oxides, exposing sites with a mixed coordination to Fe and Co, behave. By forming surface O species with a mixed Fe/Co coordination, we can investigate the nature of such sites. By means of scanning tunnelling microscopy and x-ray photoelectron spectroscopy, we characterize a series of Co-Fe oxides samples with different Fe contents at the atomic scale and observe a scaling of the hydroxylation degree with the amount of Fe inside the Co-Fe oxides. Our results indicate that the Fe dopants within the Co-Fe oxides have opposing effects on edge and basal plane sites modifying the maximum hydroxylation degree of pure cobalt oxide, perturbing the original binding sites of H, releasing the absorbed H or blocking the diffusion pathway of H.
引用
收藏
页数:9
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