Issue 8, 2016

Dynamic etching of soluble surface layers with on-line inductively coupled plasma mass spectrometry detection – a novel approach for determination of complex metal oxide surface cation stoichiometry

Abstract

In this work, an innovative approach for determining the surface stoichiometry of complex metal oxide (CMO) thin films is presented. The procedure is based on treatment of the sample surface with different etching solutions, followed by on-line analysis of the derived eluates using inductively coupled plasma – mass spectrometry (ICP-MS). Via consecutive treatment of the sample surface with water and diluted HCl, a differentiation between water soluble and acid soluble parts of near surface regions in thin films is enabled. The developed procedure was applied for the analysis of dense La0.6Sr0.4CoO3−δ (LSC) thin films indicating the presence of a water soluble Sr-rich phase with sub nm-thickness on top of the LSC films. The step-wise optimization of this technique is reported and the results are compared to measurements performed by low-energy ion scattering (LEIS). The detrimental effect of the water soluble Sr rich phase on the oxygen exchange activity of LSC thin film electrodes is verified by electrochemical impedance spectroscopy (EIS).

Graphical abstract: Dynamic etching of soluble surface layers with on-line inductively coupled plasma mass spectrometry detection – a novel approach for determination of complex metal oxide surface cation stoichiometry

Article information

Article type
Paper
Submitted
26 Apr 2016
Accepted
28 Jun 2016
First published
28 Jun 2016
This article is Open Access
Creative Commons BY license

J. Anal. At. Spectrom., 2016,31, 1638-1646

Author version available

Dynamic etching of soluble surface layers with on-line inductively coupled plasma mass spectrometry detection – a novel approach for determination of complex metal oxide surface cation stoichiometry

A. Limbeck, G. M. Rupp, M. Kubicek, H. Téllez, J. Druce, T. Ishihara, J. A. Kilner and J. Fleig, J. Anal. At. Spectrom., 2016, 31, 1638 DOI: 10.1039/C6JA00154H

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