Startseite Naturwissenschaften Chapter 3A Advances in understanding electrochemical reaction mechanisms of highly dispersed metal sites using X-ray absorption spectroscopy
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Chapter 3A Advances in understanding electrochemical reaction mechanisms of highly dispersed metal sites using X-ray absorption spectroscopy

  • Hao Zhang , Bingbao Mei und Zheng Jiang
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Nanochemistry
Ein Kapitel aus dem Buch Nanochemistry

Abstract

During the past decade, highly dispersed metal sites (HDMSs) have attracted considerable attention in electrocatalysis because of their intriguing catalytic performance and maximum efficiency of atomic utilization. These sites usually appear in single/ dual-atom catalysts or subnanometric clusters, whose long-range structures are disordered and catalytic performances are intimately correlated with coordination environments and interactions with support. When applied in reaction, these unsaturated coordination sites within HDMSs strongly interact with the environment (support, electrolyte, ligands, adsorbates, reaction products, and intermediates), leading their structures to change with the reaction conditions. In this regard, clarifying the actual structure of HDMSs is of great importance for understanding the reaction mechanism and for further catalytic optimization. X-ray absorption spectroscopy (XAS) is an indispensable technique for probing the electronic and geometric structures of HDMSs. This chapter discusses the fundamental principles of the XAS method, introduces the experimental paradigm of data collection in the transmission and fluorescence models, and describes the data analysis approaches undertaken for deciphering X-ray absorption near the edge and extended X-ray absorption fine structure spectra. Moreover, we will illustrate the XAS studies of highly dispersed metal catalysts in a wide range of electrochemical reactions and highlight the application of in situ and operando XAS for revealing the nature of the active sites and establishing links between the structural motifs in HDMSs, local electronic structures, and catalytic properties.

Abstract

During the past decade, highly dispersed metal sites (HDMSs) have attracted considerable attention in electrocatalysis because of their intriguing catalytic performance and maximum efficiency of atomic utilization. These sites usually appear in single/ dual-atom catalysts or subnanometric clusters, whose long-range structures are disordered and catalytic performances are intimately correlated with coordination environments and interactions with support. When applied in reaction, these unsaturated coordination sites within HDMSs strongly interact with the environment (support, electrolyte, ligands, adsorbates, reaction products, and intermediates), leading their structures to change with the reaction conditions. In this regard, clarifying the actual structure of HDMSs is of great importance for understanding the reaction mechanism and for further catalytic optimization. X-ray absorption spectroscopy (XAS) is an indispensable technique for probing the electronic and geometric structures of HDMSs. This chapter discusses the fundamental principles of the XAS method, introduces the experimental paradigm of data collection in the transmission and fluorescence models, and describes the data analysis approaches undertaken for deciphering X-ray absorption near the edge and extended X-ray absorption fine structure spectra. Moreover, we will illustrate the XAS studies of highly dispersed metal catalysts in a wide range of electrochemical reactions and highlight the application of in situ and operando XAS for revealing the nature of the active sites and establishing links between the structural motifs in HDMSs, local electronic structures, and catalytic properties.

Heruntergeladen am 10.12.2025 von https://www.degruyterbrill.com/document/doi/10.1515/9783110739879-007/html
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