Abstract
The distribution of ions and charge at solid-water interfaces plays an essential role in a wide range of processes in biology, geology and technology. While theoretical models of the solid-electrolyte interface date back to the early 20 th century, a detailed picture of the structure of the electric double layer has remained elusive, largely because of experimental techniques have not allowed direct observation of the behaviour of ions, i.e. with subnanometer resolution. We have made use of recent advances in high-resolution Atomic Force Microscopy to reveal, with atomic level precision, the ordered adsorption of the mono- and divalent ions that are common in natural environments to heterogeneous gibbsite/silica surfaces in contact with aqueous electrolytes. Complemented by density functional theory, our experiments produce a detailed picture of the formation of surface phases by templated adsorption of cations, anions and water, stabilized by hydrogen bonding.
| Original language | English |
|---|---|
| Article number | 4956 |
| Journal | Scientific Reports |
| Volume | 4 |
| DOIs | |
| State | Published - 22 May 2014 |
| Externally published | Yes |
Bibliographical note
Funding Information:The authors thank M. Borkovec and J.J. Lyklema for insightful discussions. We also thank Kislon Voitchovsky for providing useful hints on atomic resolution measurements, L.Verhoeff for providing a gibbsite sample for preliminary AFM experiments and Ian Collins and the BP Pushing Reservoir Limits team for discussion. Financial support was provided through the Exploratory Research (ExploRe) program of BP plc.
ASJC Scopus subject areas
- General