Low Ti Additions to Stabilize Ru‐Ir Electrocatalysts for the Oxygen Evolution Reaction

Author:

Lahn Leopold12,Mingers Andrea M.3,Savan Alan4,Ludwig Alfred4,Kasian Olga12ORCID

Affiliation:

1. Helmholtz-Zentrum Berlin GmbH Helmholtz Institut Erlangen-Nürnberg Cauerstr. 1 91058 Erlangen Germany

2. Department of Materials Science and Engineering Friedrich-Alexander-Universität Erlangen-Nürnberg 91058 Erlangen Germany

3. Max-Planck-Institut für Eisenforschung GmbH Max-Planck-Straße 1 40237 Düsseldorf Germany

4. Materials Discovery and Interfaces Institut für Werkstoffe Ruhr-Universität Bochum Gebäude IC 03/225 44780 Bochum Germany

Abstract

AbstractAnodic oxygen evolution reaction (OER) challenges large scale application of proton exchange membrane water electrolyzers (PEMWE) due to sluggish kinetics, high overpotential and extremely corrosive environment. While Ir oxides currently provide the best balance between activity and stability, the scarcity of Ir and corresponding high market price lead to poor cost‐benefit factors. Mixing Ir with more stable non‐precious Ti reduces the noble metal loading and may implicate stabilization, while addition of more catalytically active Ru ensures a high reaction rate. Here, we examine the activity‐stability behavior of Ru‐Ir‐Ti thin film material libraries with low Ti‐content under the OER conditions. The high sensitivity to the dissolution of the individual alloy components was achieved by using online and off‐line inductively coupled plasma mass spectrometry (ICP‐MS) analysis. Our data reveal that even low Ti additions improve the stability of Ru‐Ir catalysts without sacrificing activity. In particular, 5 at. % of Ti enable stability increase of Ir in the Ru‐Ir catalyst by a factor of 3. Moreover, this catalyst exhibits higher activity compared to the Ti‐free Ru‐Ir alloys with similar Ir content. Observed activity‐stability trends are discussed in light of X‐ray photoelectron spectroscopy data.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Electrochemistry,Catalysis

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