4.6 Article

Order beyond a monolayer: The story of two self-assembled 4,4′-bipyridine layers on the Sb(111) | ionic liquid interface

Journal

ELECTROCHIMICA ACTA
Volume 421, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2022.140468

Keywords

Ionic liquids; EMImBF(4); Antimony surface; Self-assembly

Funding

  1. Estonian Research Council [PSG249]
  2. EU through the European Regional Development Fund [TK141 (2014-2020.4.01.15-0011)]

Ask authors/readers for more resources

In this study, the adsorption behavior of organic molecules at the interface between a semi-metallic Sb(111) electrode and an ionic liquid was investigated. Two distinctive stacked adsorbed layers were identified, and their properties were studied using experimental methods and density functional theory calculations. These insights are of fundamental and practical importance in the development of nanoelectronic devices.
In this study, it has been shown that the ordering of organic molecules is not limited to a highly organised self-assembled monolayer on the electrode's surface. At the interface between semi-metallic Sb(111) electrode and ionic liquid with 4,4'-bipyridine addition, two distinctive stacked adsorbed layers upon each other have been identified by applying in situ scanning tunnelling microscopy and electrochemical impedance spectroscopy methods. The first adlayer in contact with the electrode consists of tightly packed ordered rows. The second adlayer, on top of the first, is characterised by low surface concentration, and its unit cell was obtained experimentally. In addition to experimental data, the likely distribution of 4,4'-bipyridine molecules in the first adlayer has been described using density functional theory calculations combined with machine learning. The gained insights of organic's adsorption from ionic liquids are of fundamental and practical importance in the development of nanoelectmnic devices.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available