X射线光电子能谱
分析化学(期刊)
化学状态
基质(水族馆)
化学
碳纤维
光谱学
结合能
化学位移
工作职能
石墨氮化碳
氮化碳
氮化物
光电发射光谱学
金属
材料科学
原子物理学
物理化学
物理
核磁共振
图层(电子)
环境化学
有机化学
催化作用
复合材料
地质学
海洋学
复合数
光催化
量子力学
作者
Grzegorz Greczyński,Lars Hultman
出处
期刊:ChemPhysChem
[Wiley]
日期:2017-03-10
卷期号:18 (12): 1507-1512
被引量:850
标识
DOI:10.1002/cphc.201700126
摘要
Abstract The C 1s signal from ubiquitous carbon contamination on samples forming during air exposure, so called adventitious carbon (AdC) layers, is the most common binding energy (BE) reference in X‐ray photoelectron spectroscopy studies. We demonstrate here, by using a series of transition‐metal nitride films with different AdC coverage, that the BE of the C 1s peak varies by as much as 1.44 eV. This is a factor of 10 more than the typical resolvable difference between two chemical states of the same element, which makes BE referencing against the C 1s peak highly unreliable. Surprisingly, we find that C 1s shifts correlate to changes in sample work function , such that the sum is constant at 289.50±0.15 eV, irrespective of materials system and air exposure time, indicating vacuum level alignment. This discovery allows for significantly better accuracy of chemical state determination than offered by the conventional methods. Our findings are not specific to nitrides and likely apply to all systems in which charge transfer at the AdC/substrate interface is negligible.
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