Erik Anderson "In situ Scanning Tunnelling Microscopy studies of the interfacial structure between Bi(111) electrode and a room temperature ionic liquid" | University of Tartu

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Jakobi 2, rooms 116–121, 51005 Tartu
  • Dean's Office
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  • Dean's Office
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  • Institute of Genomics
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  • Museum
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Erik Anderson "In situ Scanning Tunnelling Microscopy studies of the interfacial structure between Bi(111) electrode and a room temperature ionic liquid"

Date: 
28.08.2015 - 16:00

Erik Anderson will defend his PhD thesis in chemistry entitled "In situ Scanning Tunnelling Microscopy studies of the interfacial structure between Bi(111) electrode and a room temperature ionic liquid" in the Faculty of Science and Technology in the University of Tartu  (Chemicum, Ravila 14a-1021) on 28 August at 16.00.

Supervisor: Professor Enn Lust, PhD, Institute of Chemistry, University of Tartu
Opponent: Professor Pawel J. Kulesza, PhD, University of Warsaw (Poland)

Summary

Ionic liquids as electrolytes alternative to aqueous solution have gained attention in the recent years. It is well-known that the electrochemical processes in aqueous medium are often limited and much energy is lost, when overpotentials are applied, for example, in the field of electrosynthesis. In the medium of ionic liquids it is often possible to operate with the lower energy costs. For example, the deposition of noble metals and their alloys. In addition, ionic liquids are excellent candidates as solvents.

Today, there is no clear understanding about the structure at electrode | ionic liquid interface. Also, the interfacial processes in the conditions of electrochemical polarization require further studies, especially in the field of microscopy.

From the prvious works using Scanning Probe Microscopy (STM) and Atomic Force Microscopy (AFM) it is known that Bi(111) electrode is very stable under negative potential conditions in aqueous as well in non-aqueous medium. The Bi(111) electrode is a viable alternative to Au(hkl) or carbon electrodes. Additionally, in the medium of ionic liquid, it is usually possible to study potentials which are not possible in aqueous solutions. As a result, new processes can be studied on the Bi(111) electrode.

Main aim of the present PhD thesis is to study the interface between Bi(111) electrode and an ionic liquid usin in situ STM method. Three ionic liquids were chosen: 1-ethyl-3-methylimidazolium tetrafluoroborate, 1-butyl-4-methylpyridinium tetrafluoro-borate, and a mixture of 1-ethyl-3-methylimidazolium tetrafluoro-borate + 1-ethyl-3-methylimidazolium iodide. In present PhD thesis, cyclic voltammetry and electrochemical impedance spectroscopy were used as complementary methods.

In the PhD thesis, it was demonstrated that Bi(111) electrode in ionic liquids studied has atomically flat surface, comparable with the results obtained for Bi(111) electrode in aqueous solutions. For all three ionic liquids atomic resolution for Bi(111) electrode was established. It was also proven that Bi(111) electrode is time stable under changing negative potential conditions during hours in ionic liquid medium. In addition, the adsorption of iodide anions was visualized at Bi(111) electrode surface from a mixture of ionic liquids.

In the PhD thesis, the surfaces of cathodes, anodes and electrolytes of Solid Oxide Fuel Cell (SOFC) were studied with AFM method. The grainy structure of SOFC electrodes was modelled with special hardware and the following characteristics were obtained: medium grain diameter, grain distribution on surface and and Root Mean Square roughness.

In addition, the method of grain analysis was further elaborated and has been applied for Bi(111) | ionic liquid interface. The adsorbed anions on Bi(111) surface from a mixture of 1-ethyl-3-methylimidazolium tetrafluoro-borate + 1-ethyl-3-methyl-imidazolium iodide, and the anisotropic dissolution of Bi(111) from 1-ethyl-3-methylimidazolium tetrafluoroborate were modelled. The average ion diameters, and the average diameter dissolution / deposition islands on Bi(111) electrode surface were measured, respectively.

 

Location: 
Chemicum, Ravila 14a-1021
Event category: