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Graphene-Capped Liquid Thin Films for Electrochemical Operando X-ray Spectroscopy and Scanning Electron Microscopy

[Image: see text] Electrochemistry is a promising building block for the global transition to a sustainable energy market. Particularly the electroreduction of CO(2) and the electrolysis of water might be strategic elements for chemical energy conversion. The reactions of interest are inner-sphere r...

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Detalles Bibliográficos
Autores principales: Falling, Lorenz J., Mom, Rik V., Sandoval Diaz, Luis E., Nakhaie, Siamak, Stotz, Eugen, Ivanov, Danail, Hävecker, Michael, Lunkenbein, Thomas, Knop-Gericke, Axel, Schlögl, Robert, Velasco-Vélez, Juan-Jesús
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458360/
https://www.ncbi.nlm.nih.gov/pubmed/32702231
http://dx.doi.org/10.1021/acsami.0c08379
Descripción
Sumario:[Image: see text] Electrochemistry is a promising building block for the global transition to a sustainable energy market. Particularly the electroreduction of CO(2) and the electrolysis of water might be strategic elements for chemical energy conversion. The reactions of interest are inner-sphere reactions, which occur on the surface of the electrode, and the biased interface between the electrode surface and the electrolyte is of central importance to the reactivity of an electrode. However, a potential-dependent observation of this buried interface is challenging, which slows the development of catalyst materials. Here we describe a sample architecture using a graphene blanket that allows surface sensitive studies of biased electrochemical interfaces. At the examples of near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and environmental scanning electron microscopy (ESEM), we show that the combination of a graphene blanket and a permeable membrane leads to the formation of a liquid thin film between them. This liquid thin film is stable against a water partial pressure below 1 mbar. These properties of the sample assembly extend the study of solid–liquid interfaces to highly surface sensitive techniques, such as electron spectroscopy/microscopy. In fact, photoelectrons with an effective attenuation length of only 10 Å can be detected, which is close to the absolute minimum possible in aqueous solutions. The in-situ cells and the sample preparation necessary to employ our method are comparatively simple. Transferring this approach to other surface sensitive measurement techniques should therefore be straightforward. We see our approach as a starting point for more studies on electrochemical interfaces and surface processes under applied potential. Such studies would be of high value for the rational design of electrocatalysts.