Increasing Activity of Trimetallic Oxygen Reduction PtNiMo/C Catalysts Through Initial Conditioning

Author:

Danisman Bilal1ORCID,Zhang Gui‐Rong12,Baumunk Adrian F.13,Yang Juntao4,Brummel Olaf4ORCID,Darge Philipp5,Dworschak Dominik5,Mayrhofer Karl J. J.5,Libuda Jörg4,Zhou Xin6,Wu Mingjian6,Spiecker Erdmann6,Ledendecker Marc17,Etzold Bastian J. M.13ORCID

Affiliation:

1. Department of Chemistry Ernst-Berl-Institute for Technical and Macromolecular Chemistry Technical University of Darmstadt 64287 Darmstadt Germany

2. School of Chemical Engineering and Technology Tiangong University BinShuiXi Road 399 Tianjin 300387 China

3. Department of Chemical and Biological Engineering Power-to-X Technologies FAU Erlangen-Nürnberg Egerlandstr. 3 91058 Erlangen Germany

4. Erlangen Center for Interface Research and Catalysis FAU Erlangen-Nürnberg Egerlandstr. 3 91058 Erlangen Germany

5. Forschungszentrum Jülich GmbH Helmholtz-Institute Erlangen-Nürnberg for Renewable Energy (IEK-11) Cauerstr. 1 91058 Erlangen Germany

6. Institute of Micro- and Nanostructure Research (IMN) & Center for Nanoanalysis and Electron Microscopy (CENEM) Interdisciplinary Center for Nanostructured Films (IZNF) Department of Materials Science and Engineering Friedrich-Alexander-Universität Erlangen-Nürnberg Cauerstrasse 3 91058 Erlangen Germany

7. Sustainable Energy Materials Campus Straubing for Biotechnology and Sustainability Technical University of Munich Schulgasse 22 94315 Straubing Germany

Abstract

AbstractThis study investigates the importance of preconditioning in Pt‐alloy catalysts for oxygen–reduction reactions. Previous research indicated that slower scanning rates during preconditioning initially boost activity, but this is followed by a rapid decline. The study reveals the required number of cycles to achieve the first constant steady state activity in PtNiMo/C catalysts when using slower scanning rates during preconditioning. It also highlights the resulting activity differences. Remarkably, a catalyst preconditioned with 150 slow cycles showed an activity of approximately 1.25 mA cm−2 at 0.90 VRHE, significantly higher than one preconditioned at a fast rate (0.82 mA cm−2). Both ex–situ and in–situ analyses revealed that Pt, along with Ni, was leached during pretreatment. At slower scan rates of 20 mV s−1, the dissolved Pt redeposited as highly active, small‐sized clusters or single atoms. Fast scan rates of of 500 mV s−1, in contrast, resulted in fewer such clusters. Accelerated stress tests up to 1.10 VRHE confirmed the high stability of these clusters, demonstrating a substantial activity increase even after 24,000 cycles.

Funder

Deutsche Forschungsgemeinschaft

China Scholarship Council

National Natural Science Foundation of China

Publisher

Wiley

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