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C 1s Peak of Adventitious Carbon Aligns to the Vacuum Level: Dire Consequences for Materials Bonding Assignment by Photoelectron Spectroscopy

机译:不定碳的C 1s峰与真空水平对齐:光电子光谱法确定材料键合的可怕后果

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摘要

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 EBF 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 ϕSA , such that the sum EBF+ϕSA 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.
机译:来自X射线光电子能谱研究中最常见的结合能(BE)参考是来自暴露于空气中样品上普遍存在的碳污染的C 1s信号,即所谓的不定碳(AdC)层。我们在这里通过使用一系列具有不同AdC覆盖率的过渡金属氮化物膜来证明C 1s的BE峰 E B F 的差异高达1.44 eV。这比同一元素的两种化学状态之间的典型可分辨差异大10倍,这使得BE参照C 1s峰非常不可靠。令人惊讶地,我们发现C 1s移位与样本功函数ϕSA的变化相关,因此总和 E B F + ϕ S A 恒定在289.50±0.15 eV,与材料系统和空气暴露时间无关,这表明真空水平对准。该发现使化学状态确定的准确性大大优于常规方法。我们的发现并非特定于氮化物,并且可能适用于在AdC /基板界面上的电荷转移可忽略不计的所有系统。

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