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Abstract Native oxides form on the surface of many metals. Here, using gallium‐based liquid metal alloys, Johnson‐Kendall‐Roberts (JKR) measurements are employed to show that native oxide dramatically lower the tension of the metal interface from 724 to 10 mN m−1. Like conventional surfactants, the oxide has asymmetry between the composition of its internal and external interfaces. Yet, in comparison to conventional surfactants, oxides are an order of magnitude more effective at lowering tension and do not need to be added externally to the liquid (i.e., oxides form naturally on metals). This surfactant‐like asymmetry explains the adhesion of oxide‐coated metals to surfaces. The resulting low interfacial energy between the metal and the interior of the oxide helps stabilize non‐spherical liquid metal structures. In addition, at small enough macroscopic contact angles, the finite tension of the liquid within the oxide can drive fluid instabilities that are useful for separating the oxide from the metal to form oxide‐encased bubbles or deposit thin oxide films (1–5 nm) on surfaces. Since oxides form on many metals, this work can have implications for a wide range of metals and metal oxides in addition to explaining the physical behavior of liquid metal.
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The coordination chemistry of oxide and nanocarbon materials
Understanding how a ligand affects the steric and electronic properties of a metal is the cornerstone of the inorganic chemistry enterprise. What happens when the ligand is an extended surface? This question is central to the design and implementation of state-of-the-art functional materials containing transition metals. This perspective will describe how these two very different sets of extended surfaces can form well-defined coordination complexes with metals. In the Green formalism, functionalities on oxide surfaces react with inorganics to form species that contain X-type or LX-type interactions between the metal and the oxide. Carbon surfaces are neutral L-type ligands; this perspective focuses on carbons that donate six electrons to a metal. The nature of this interaction depends on the curvature, and thereby orbital overlap, between the metal and the extended π-system from the nanocarbon.
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- Award ID(s):
- 2101582
- PAR ID:
- 10410335
- Date Published:
- Journal Name:
- Dalton Transactions
- Volume:
- 51
- Issue:
- 22
- ISSN:
- 1477-9226
- Page Range / eLocation ID:
- 8557 to 8570
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/D2DT00459C
