Abstract
At an electrified interface the double-layer problem plays a key role. Its characteristics for ionic liquids are discussed on the basis of recent experimental and theoretical investigations and are contrasted with the classical GCS model for aqueous electrolytes. Emphasis of this chapter is on 2D and 3D electrochemical phase formation and growth at the ionic liquid/electrode interface studied by in situ scanning probe methods. The concept of underpotential (UPD) deposition is briefly introduced and for the example of Ag UPD on Au(111) the different behaviour in an ionic liquid and aqueous electrolytes is described. Phenomena of surface alloying and the underlying spinodal mechanism are treated in more detail. The characteristic spinodal structures and their evolution during surface alloying in Zn − Au(111) and Cd − Au(111) are presented. Nanoscale electrochemical phase formation and growth of metal and semiconductor clusters from ionic liquid electrolytes is the topic of the last section. Selected examples are Al electrodeposition on Si(111):H, Ni, and Fe nanocrystal growth; Co − Al bulk alloying; and AlSb and ZnSb compound semiconductor deposition. The chapter ends with an example of a thickness induced metal–nonmetal transition in ultrathin Ge films electrodeposited on Au(111) or Si(111):H.
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Notes
- 1.
The solid electrode can be metal, semi-metal such as highly oriented pyrolytic graphite (HOPG), or semiconductor, but here we focus on metal electrodes.
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Freyland, W. (2011). Electrified Ionic Liquid/Solid Interfaces. In: Coulombic Fluids. Springer Series in Solid-State Sciences, vol 168. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-17779-8_5
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