Klyushin Alexander Yu, Rocha Tulio C R, Hävecker Michael, Knop-Gericke Axel, Schlögl Robert
Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, 14195, Berlin, Germany.
Phys Chem Chem Phys. 2014 May 7;16(17):7881-6. doi: 10.1039/c4cp00308j.
The surface of a gold foil under ozone oxidation was examined by near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and scanning electron microscopy (SEM). Our in situ observations show that a surface oxide phase is formed during the exposure to ozone; however this phase decomposes under vacuum and even in the presence of ozone at temperatures higher than 300 °C. Assuming that an oxide overlayer completely covers the Au surface, the thickness of the oxide phase was estimated to be between 0.29 and 0.58 nm by energy-dependent XPS depth profiling. The surface oxidation led to structural modifications of the gold surface. These morphological changes do not disappear even under vacuum. In the Au 4f spectra, an additional component at low binding energy (83.3 eV), which appears during/after O3 treatment, is assigned to the presence of low-coordinated atoms which appear on the Au surface as a result of surface restructuring under oxidation. Ex situ SEM images demonstrate that only the region of the sample that was exposed to O3 shows the presence of ridges on the Au surface.
采用近常压X射线光电子能谱(NAP-XPS)和扫描电子显微镜(SEM)对臭氧氧化作用下金箔的表面进行了检测。我们的原位观察表明,在暴露于臭氧的过程中会形成表面氧化物相;然而,该相在真空中以及在温度高于300°C时即使存在臭氧的情况下也会分解。假设氧化物覆盖层完全覆盖金表面,通过能量相关的XPS深度剖析估计氧化物相的厚度在0.29至0.58纳米之间。表面氧化导致了金表面的结构改性。即使在真空中,这些形态变化也不会消失。在Au 4f光谱中,在O3处理期间/之后出现的低结合能(83.3 eV)处的一个额外成分被归因于由于氧化作用下的表面重构而在金表面出现的低配位原子的存在。非原位SEM图像表明,只有样品中暴露于O3的区域在金表面显示出脊状结构。