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通过原位处理理解 XPS 中氧化镧的结合能校准。

Understanding of binding energy calibration in XPS of lanthanum oxide by in situ treatment.

机构信息

School of Physical Science and Technology, ShanghaiTech University, 100 Haike Road, Shanghai, 201210, China.

Shell Global Solutions International B.V, Amsterdam, 1031 CM, The Netherlands.

出版信息

Phys Chem Chem Phys. 2019 Oct 28;21(40):22351-22358. doi: 10.1039/c9cp04187g. Epub 2019 Oct 2.

Abstract

Rare earth oxides have seen increased usage over the years in batteries and catalysts. Due to their unique electronic properties, they are the subject of fundamental and practical interest. However, the complexity in their electronic structures makes unambiguous characterization, such as X-ray photoelectron spectroscopy (XPS), very challenging. Lanthanum oxide (LaO) has attracted special attention as a promising catalyst for the oxidative coupling of methane (OCM) reaction. In this work, a new and reliable way of XPS calibration is developed by applying various in situ preparations for a nanorod LaO catalyst to intentionally form different lanthanum compounds, followed by XPS characterization and corroboration with first principles calculations. To form different compounds, five sample treatments were performed including heating in vacuum and treatment with O, CH, CO, and HO, which are all relevant to OCM reaction conditions. Adventitious carbon or lattice oxygen, as conventional calibration standard species for energy scale, is only suitable for one or few in situ prepared surfaces. Our results also clearly demonstrate the vital difference between performing the ex situ analysis after exposure of the sample to the atmosphere and the in situ analysis. By carefully comparing the spectra of various photoemission peaks of different compounds, we conclude that the binding energy of 102.2 eV for the La 4d peak can be used as the internal calibration standard for all considered samples. Furthermore, different oxygen species were unambiguously identified by matching the oxygen 1s binding energies from the in situ measurements and first principles predictions.

摘要

多年来,稀土氧化物在电池和催化剂中得到了越来越多的应用。由于其独特的电子特性,它们成为基础和实际研究的课题。然而,其电子结构的复杂性使得明确的特性描述,如 X 射线光电子能谱(XPS),变得极具挑战性。氧化镧(LaO)作为一种有前途的甲烷氧化偶联(OCM)反应催化剂,引起了特别关注。在这项工作中,通过对纳米棒 LaO 催化剂进行各种原位制备,应用于有意形成不同镧化合物的方法,开发了一种新的、可靠的 XPS 校准方法,然后进行 XPS 表征,并与第一性原理计算相吻合。为了形成不同的化合物,进行了五种样品处理,包括在真空中加热以及用 O、CH、CO 和 HO 处理,这些处理都与 OCM 反应条件有关。通常用作能标校准标准物质的非定域态碳或晶格氧,仅适用于一种或几种原位制备的表面。我们的结果还清楚地表明,在将样品暴露于大气后进行的非原位分析与原位分析之间存在重要差异。通过仔细比较不同化合物的各种光致发射峰的光谱,我们得出结论,La 4d 峰的结合能为 102.2 eV 可用于所有考虑的样品的内部校准标准。此外,通过匹配原位测量和第一性原理预测的氧 1s 结合能,可明确地识别出不同的氧物种。

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