Review-In Situ X-ray and Infrared Spectroscopic Studies of Electrochemical Systems

被引:0
|
作者
Marinkovic, Nebojsa S. [1 ,2 ]
Sasaki, Kotaro [3 ]
Adzic, Radoslav R. [3 ]
机构
[1] Columbia Univ, Synchrotron Catalysis Consortium, New York, NY 10027 USA
[2] Columbia Univ, New York, NY 10027 USA
[3] Brookhaven Natl Lab, Upton, NY 11973 USA
关键词
infrared spectroscopy; X-ray absorption spectroscopy; electrocatalysis; fuel cells; ETHANOL OXIDATION; FTIR SPECTROSCOPY; OXIDIZING ETHANOL; ELECTROOXIDATION; ELECTROCATALYSTS; PLATINUM; REFLECTION; ADSORPTION; ELECTRODES; CATALYSTS;
D O I
10.1149/1945-7111/ad91e3
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Despite of intense research and a wealth of data, the phenomena occurring during electrocatalysis are still a major obstacle in many chemical processes. Molecular analysis of the electrode/electrolyte interface is needed to correctly describe the reaction through identifying the species involved, their interaction with the environment and kinetics in situ, i.e. while the reaction is taking place. That can be done by coupling the electrochemical system with complementary non-electrochemical techniques. Particularly revealing are in situ X-ray spectroscopic techniques to analyze the electrode itself, providing the information on the changes in the catalyst during the reaction. The synergy of the traditional electrochemical techniques with the complementary spectroscopic methodologies offer understanding of the electrode/electrolyte interface above and beyond traditional experimental mainframe. Here we demonstrate how in situ X-ray absorption spectroscopy (XAS), in situ infrared reflection/absorption spectroscopy (IRRAS), and traditional voltammetric studies can increase our understanding of electrochemical processes during oxidation of ethanol. The results show the pronounced role of electrode surface in determining reaction kineticks and revealed the selectivity of the catalyst to complete oxidation pathway. They further provide understanding of the parameters that enhance its oxidation for future designing catalysts for alcohol oxidation fuel cells. (c) 2024 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, https://creativecommons.org/ licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited.
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页数:8
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