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杂质碳的C 1s峰与真空能级对齐:对光电子能谱法确定材料键合的严重影响。

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

作者信息

Greczynski Grzegorz, Hultman Lars

机构信息

Thin Film Physics Division, Department of Physics (IFM), Linköping University, SE-581 83, Linköping, Sweden.

出版信息

Chemphyschem. 2017 Jun 20;18(12):1507-1512. doi: 10.1002/cphc.201700126. Epub 2017 Apr 11.

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 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.

摘要

在空气暴露过程中样品上形成的普遍存在的碳污染,即所谓的不定碳(AdC)层,其C 1s信号是X射线光电子能谱研究中最常见的结合能(BE)参考。我们在此通过使用一系列具有不同AdC覆盖率的过渡金属氮化物薄膜证明,C 1s峰的BE(EBF)变化高达1.44 eV。这比同一元素的两个化学态之间的典型可分辨差异大10倍,这使得以C 1s峰为参考的BE高度不可靠。令人惊讶的是,我们发现C 1s位移与样品功函数ϕSA的变化相关,使得EBF + ϕSA之和在289.50±0.15 eV时保持恒定,与材料体系和空气暴露时间无关,表明真空能级对齐。这一发现使得化学态测定的准确性比传统方法有显著提高。我们的发现并非特定于氮化物,可能适用于所有在AdC/衬底界面电荷转移可忽略不计的系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/5484993/bea796c27568/CPHC-18-1507-g001.jpg

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