Molecular Analysis of the Unusual Stability of an IrNbO x Catalyst for the Electrochemical Water Oxidation to Molecular Oxygen (OER)

• Published in: ACS applied materials & interfaces 2021-01, Vol.13 (3), p.3748-3761
• Main Authors: Spöri, Camillo, Falling, Lorenz J, Kroschel, Matthias, Brand, Cornelius, Bonakdarpour, Arman, Kühl, Stefanie, Berger, Dirk, Gliech, Manuel, Jones, Travis E, Wilkinson, David P, Strasser, Peter
• Format: Article
• Language: English
• Subjects: Energy, Environmental, and Catalysis Applications
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/acsami.0c12609

Adoption of proton exchange membrane (PEM) water electrolysis technology on a global level will demand a significant reduction of today’s iridium loadings in the anode catalyst layers of PEM electrolyzers. However, new catalyst and electrode designs with reduced Ir content have been suffering from limited stability caused by (electro)­chemical degradation. This has remained a serious impediment to a wider commercialization of larger-scale PEM electrolysis technology. In this combined DFT computational and experimental study, we investigate a novel family of iridium–niobium mixed metal oxide thin-film catalysts for the oxygen evolution reaction (OER), some of which exhibit greatly enhanced stability, such as minimized voltage degradation and reduced Ir dissolution with respect to the industry benchmark IrO x catalyst. More specifically, we report an unusually durable IrNbO x electrocatalyst with improved catalytic performance compared to an IrOx benchmark catalyst prepared in-house and a commercial benchmark catalyst (Umicore Elyst Ir75 0480) at significantly reduced Ir catalyst cost. Catalyst stability was assessed by conventional and newly developed accelerated degradation tests, and the mechanistic origins were analyzed and are discussed. To achieve this, the IrNbO x mixed metal oxide catalyst and its water splitting kinetics were investigated by a host of techniques such as synchrotron-based NEXAFS analysis and XPS, electrochemistry, and ab initio DFT calculations as well as STEM-EDX cross-sectional analysis. These analyses highlight a number of important structural differences to other recently reported bimetallic OER catalysts in the literature. On the methodological side, we introduce, validate, and utilize a new, nondestructive XRF-based catalyst stability monitoring technique that will benefit future catalyst development. Furthermore, the present study identifies new specific catalysts and experimental strategies for stepwise reducing the Ir demand of PEM water electrolyzers on their long way toward adoption at a larger scale.