Unraveling Catalytic Reaction Mechanism by In Situ Near Ambient Pressure X-ray Photoelectron Spectroscopy

被引:19
|
作者
Lian, Xu [1 ]
Gao, Jiajia [1 ]
Ding, Yishui [1 ,2 ]
Liu, Yuan [1 ,2 ]
Chen, Wei [1 ,2 ,3 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Tianjin Univ, Joint Sch Natl Univ Singapore, Fuzhou 350207, Peoples R China
[3] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2022年 / 13卷 / 35期
基金
新加坡国家研究基金会;
关键词
GAS-SHIFT REACTION; METHANOL SYNTHESIS; MOLYBDENUM CARBIDE; HYDROGEN ADSORPTION; ULTRAHIGH-VACUUM; MODEL CATALYSTS; ACTIVE SURFACE; CARBON-DIOXIDE; CO OXIDATION; INTERFACES;
D O I
10.1021/acs.jpclett.2c01191
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
Probing surface chemistry during reactions closer to realistic conditions is crucial for the understanding of mechanisms in heterogeneous catalysis. Near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) is one of the state-of-the-art surface sensitive techniques used to characterize catalyst surfaces in gas phases. This Perspective begins with a brief overview of the development of the NAP-XPS technique and its representative applications in identifying the active sites at a molecular level. Next, recent in situ NAP-XPS investigations of several model catalysts in the CO2 hydrogenation reaction are mainly discussed. Finally, we highlight the major challenges facing NAP-XPS and future improvements to facilities for probing intermediates with higher resolutions under real ambient pressure reactions in heterogeneous catalysis.
引用
收藏
页码:8264 / 8277
页数:14
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