Time-resolved in situ vibrational spectroscopy for electrocatalysis: challenge and opportunity
Understanding the structure-activity relationship of catalysts and the reaction pathway is crucial for designing efficient, selective, and stable electrocatalytic systems. vibrational spectroscopy provides a unique tool for decoding molecular-level factors involved in electrocatalytic reactions. Typ...
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Veröffentlicht in: | Frontiers in chemistry 2023-07, Vol.11, p.1231886-1231886 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Understanding the structure-activity relationship of catalysts and the reaction pathway is crucial for designing efficient, selective, and stable electrocatalytic systems.
vibrational spectroscopy provides a unique tool for decoding molecular-level factors involved in electrocatalytic reactions. Typically, spectra are recorded when the system reaches steady states under set potentials, known as steady-state measurements, providing static pictures of electrode properties at specific potentials. However, transient information that is crucial for understanding the dynamic of electrocatalytic reactions remains elusive. Thus, time-resolved
vibrational spectroscopies are developed. This mini review summarizes time-resolved
infrared and Raman techniques and discusses their application in electrocatalytic research. With different time resolutions, these time-resolved techniques can capture unique dynamic processes of electrocatalytic reactions, short-lived intermediates, and the surface structure revolution that would be missed in steady-state measurements alone. Therefore, they are essential for understanding complex reaction mechanisms and can help unravel important molecular-level information hidden in steady states. Additionally, improving spectral time resolution, exploring low/ultralow frequency detection, and developing operando time-resolved devices are proposed as areas for advancing time-resolved techniques and their further applications in electrocatalytic research. |
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ISSN: | 2296-2646 2296-2646 |
DOI: | 10.3389/fchem.2023.1231886 |