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Water at charged interfaces

Publikationstyp
Review Article
Date Issued
2021-07-01
Sprache
English
Author(s)
Gonella, Grazia
Backus, Ellen H.G.
Nagata, Yuki
Bonthuis, Douwe J.
Loche, Philip  
Schlaich, Alexander  
Netz, Roland R.  
Kühnle, Angelika
McCrum, Ian T.
Wolf, Martin
Koper, Marc T.M.  
Winter, Bernd
Meijer, Gerard
Campen, R. Kramer
Bonn, Mischa
TORE-URI
https://hdl.handle.net/11420/55108
Journal
Nature Reviews Chemistry  
Volume
5
Issue
7
Start Page
466
End Page
485
Citation
Nature Reviews Chemistry 5 (7): 466-485 (2021)
Publisher DOI
10.1038/s41570-021-00293-2
Scopus ID
2-s2.0-85108644399
The ubiquity of aqueous solutions in contact with charged surfaces and the realization that the molecular-level details of water–surface interactions often determine interfacial functions and properties relevant in many natural processes have led to intensive research. Even so, many open questions remain regarding the molecular picture of the interfacial organization and preferential alignment of water molecules, as well as the structure of water molecules and ion distributions at different charged interfaces. While water, solutes and charge are present in each of these systems, the substrate can range from living tissues to metals. This diversity in substrates has led to different communities considering each of these types of aqueous interface. In this Review, by considering water in contact with metals, oxides and biomembranes, we show the essential similarity of these disparate systems. While in each case the classical mean-field theories can explain many macroscopic and mesoscopic observations, it soon becomes apparent that such theories fail to explain phenomena for which molecular properties are relevant, such as interfacial chemical conversion. We highlight the current knowledge and limitations in our understanding and end with a view towards future opportunities in the field. [Figure not available: see fulltext.]
DDC Class
620: Engineering
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