X射线光电子能谱
催化作用
表征(材料科学)
纳米技术
材料科学
反应机理
反应条件
化学反应
多相催化
反应中间体
光谱学
化学物理
生化工程
组合化学
机制(生物学)
电子结构
化学工程
作者
Yunxi Jiang,Dandan Cui,Weichang Hao,Ming Yang,Wei Cai,Yi Du
标识
DOI:10.1021/acsami.6c09094
摘要
With the rapid development of catalytic science, research has shifted from empirical exploration toward a mechanistic understanding of catalytic processes. In this context, probing surface chemical properties under realistic reaction conditions is essential for uncovering reaction mechanisms and guiding the development of improved catalytic materials. Conventional surface-sensitive techniques, however, are often limited to ultrahigh-vacuum environments and thus cannot fully capture the complexity of practical catalytic systems. Near-ambient-pressure X-ray photoelectron spectroscopy (NAP-XPS), also commonly referred to as ambient-pressure XPS (AP-XPS), has emerged as a powerful characterization tool that narrows this gap by enabling surface analysis under millibar- to bar-level reaction environments. By directly monitoring elemental composition, chemical states, and electronic structures, NAP-XPS provides unique insights into active site identification, catalyst dynamic reconstruction, reaction intermediate detection, and reaction pathway investigation. Here, we review recent progress in the application of NAP-XPS to heterogeneous catalysis, highlighting its contributions to mechanistic understanding. We also discuss current instrumental limitations, challenges in spectral interpretation, and future opportunities for advancing both the methodology and applications of NAP-XPS in catalytic research.
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