Issue 19, 2014

Correlating surface cation composition and thin film microstructure with the electrochemical performance of lanthanum strontium cobaltite (LSC) electrodes

Abstract

La0.6Sr0.4CoO3−δ thin films of varying thicknesses (20–170 nm) were prepared by pulsed laser deposition on yttria-stabilized zirconia (100) substrates, and their electrochemical electrode performance was correlated with the chemical surface composition and microstructure (e.g. porosity, surface area). The surface cation composition was analyzed by an atomic etching procedure with on-line inductively coupled plasma optical emission spectrometry detection. The surface sensitivity of the method was increased by dynamically switching the etching reagent during the on-line analysis and quantitative results for even the top atomic layer were obtained. A water-soluble Sr-rich surface species could be quantified on top of the LSC films and in combination with electrochemical analysis of the films by impedance spectroscopy an improved understanding of the surface exchange resistance could be obtained. Microstructural features such as the effective porosity of the films became accessible by a combination of these methods.

Graphical abstract: Correlating surface cation composition and thin film microstructure with the electrochemical performance of lanthanum strontium cobaltite (LSC) electrodes

Article information

Article type
Paper
Submitted
20 Dec 2013
Accepted
26 Feb 2014
First published
26 Feb 2014
This article is Open Access
Creative Commons BY license

J. Mater. Chem. A, 2014,2, 7099-7108

Author version available

Correlating surface cation composition and thin film microstructure with the electrochemical performance of lanthanum strontium cobaltite (LSC) electrodes

G. M. Rupp, A. Limbeck, M. Kubicek, A. Penn, M. Stöger-Pollach, G. Friedbacher and J. Fleig, J. Mater. Chem. A, 2014, 2, 7099 DOI: 10.1039/C3TA15327D

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