Lab-based ambient pressure X-ray photoelectron spectroscopy from past to present

被引:56
|
作者
Arble, Chris [1 ]
Jia, Meng [1 ]
Newberg, John T. [1 ]
机构
[1] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
关键词
Photoemission; Operando; Surface; Interface; Uptake; Catalysis; WATER-GAS SHIFT; CORE-ELECTRON-SPECTROSCOPY; IN-SITU CHARACTERIZATION; PHASE-TRANSFER CATALYSTS; NITRIC-OXIDE ADSORPTION; LEAN-BURN CONDITIONS; C-O BOND; SURFACE-CHEMISTRY; PARTIAL OXIDATION; MODEL CATALYSTS;
D O I
10.1016/j.surfrep.2018.02.002
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Chemical interactions which occur at a heterogeneous interface between a gas and substrate are critical in many technological and natural processes. Ambient pressure X-ray photoelectron spectroscopy ( APXPS) is a powerful spectroscopy tool that is inherently surface sensitive, elemental and chemical specific, with the ability to probe sample surfaces in the presence of a gas phase. In this review, we discuss the evolution of lab-based AP-XPS instruments, from the first development by Siegbahn and coworkers up through modern day systems. A comprehensive overview is given of heterogeneous experiments investigated to date via lab-based AP-XPS along with the different instrumental metrics that affect the quality of sample probing. We conclude with a discussion of future directions for lab-based AP-XPS, highlighting the efficacy for this in-demand instrument to continue to expand in its ability to significantly advance our understanding of surface chemical processes under in situ conditions in a technologically multidisciplinary setting. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 57
页数:21
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