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Probing Surface Electrochemical Activity of Nanomaterials using a Hybrid Atomic Force Microscope-Scanning Electrochemical Microscope (AFM-SECM)
Published on: February 10, 2021
The interface ionic liquid(s)/electrode(s): in situ STM and AFM measurements.
Frank Endres1, Natalia Borisenko, Sherif Zein El Abedin
1Institute of Particle Technology, Clausthal University of Technology, Arnold-Sommerfeld-Strasse 6, 38678 Clausthal-Zellerfeld, Germany. frank.endres@tu-clausthal.de
The structure of ionic liquid/electrode interfaces is complex, with layers forming and changing based on electrode potential and solute presence. Ionic liquid interfacial layers can shift from repulsive to attractive forces with added solutes like LiCl.
Area of Science:
- Electrochemistry
- Surface Science
- Materials Science
Background:
- Ionic liquids are promising electrolytes due to their stability.
- Understanding the electrode/ionic liquid interface is crucial for electrochemical applications.
- The structure of this interface is known to be complex.
Purpose of the Study:
- To investigate the nanoscale structure of the interfacial layer between an ionic liquid and Au(111).
- To examine how electrode potential and solute addition affect the interfacial structure.
Main Methods:
- In situ scanning tunneling microscopy (STM) was used to observe interfacial layers.
- Atomic force microscopy (AFM) data on anion adsorption and forces were incorporated.
Main Results:
- STM revealed the formation of layers/islands with increasing electrode potential.
- Anion adsorption strengthens with increasing potential, forming multiple layers.
- These interfacial layers exhibit nanoscale structure and are non-uniform.
- Solute addition, specifically LiCl, significantly alters the interfacial structure and forces.
Conclusions:
- The electrode/ionic liquid interface is highly complex and structured at the nanoscale.
- Electrode potential and solute presence are critical factors controlling interfacial layer formation and properties.
- Solutes can drastically change the nature of forces at the ionic liquid/electrode interface.
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