Determining materials for energy conversion across scales: The alkaline oxygen evolution reaction

Author:

Gerschel Philipp1,Angel Steven2,Hammad Mohaned3,Olean‐Oliveira André45,Toplak Blaž3ORCID,Chanda Vimanshu4,Martínez‐Hincapié Ricardo6,Sanden Sebastian1,Khan Ali Raza6,Xing Da7,Amin Amin Said3,Wiggers Hartmut25,Hoster Harry578,Čolić Viktor56,Andronescu Corina45,Schulz Christof25,Apfel Ulf‐Peter19ORCID,Segets Doris35

Affiliation:

1. Inorganic Chemistry I—Technical Electrochemistry Ruhr‐Universität Bochum Bochum Germany

2. Institute for Energy and Materials Processes—Reactive Fluids University of Duisburg‐Essen Duisburg Germany

3. Institute for Energy and Materials Processes—Particle Science and Technology University of Duisburg‐Essen Duisburg Germany

4. Chemical Technology III University of Duisburg‐Essen Duisburg Germany

5. Center for Nanointegration Duisburg‐Essen University of Duisburg‐Essen Duisburg Germany

6. Electrochemistry for Energy Conversion Max Planck Institute for Chemical Energy Conversion Mülheim an der Ruhr Germany

7. Energy Technology University of Duisburg‐Essen Duisburg Germany

8. The Hydrogen and Fuel Cell Center ZBT GmbH Duisburg Germany

9. Department of Electrosynthesis Fraunhofer UMSICHT Oberhausen Germany

Abstract

AbstractDespite considerable efforts to develop electrolyzers for energy conversion, progress has been hindered during the implementation stage by different catalyst development requirements in academic and industrial research. Herein, a coherent workflow for the efficient transition of electrocatalysts from basic research to application readiness for the alkaline oxygen evolution reaction is proposed. To demonstrate this research approach, La0.8Sr0.2CoO3 is selected as a catalyst, and its electrocatalytic performance is compared with that of the benchmark material NiFe2O4. The La0.8Sr0.2CoO3 catalyst with the desired dispersity is successfully synthesized by scalable spray‐flame synthesis. Subsequently, inks are formulated using different binders (Nafion®, Naf; Sustainion®, Sus), and nickel substrates are spray coated, ensuring a homogeneous catalyst distribution. Extensive electrochemical evaluations, including several scale‐bridging techniques, highlight the efficiency of the La0.8Sr0.2CoO3 catalyst. Experiments using the scanning droplet cell (SDC) indicate good lateral homogeneity for La0.8Sr0.2CoO3 electrodes and NiFe2O4‐Sus, while the NiFe2O4‐Naf film suffers from delamination. Among the various half‐cell techniques, SDC proves to be a valuable tool to quickly check whether a catalyst layer is suitable for full‐cell‐level testing and will be used for the fast‐tracking of catalysts in the future. Complementary compression and flow cell experiments provide valuable information on the electrodes' behavior upon exposure to chemical and mechanical stress. Finally, parameters and conditions simulating industrial settings are applied using a zero‐gap cell. Findings from various research fields across different scales obtained based on the developed coherent workflow contribute to a better understanding of the electrocatalytic system at the early stages of development and provide important insights for the evaluation of novel materials that are to be used in large‐scale industrial applications.

Funder

Fraunhofer-Gesellschaft

Mercator Research Center Ruhr

Deutsche Forschungsgemeinschaft

Publisher

Wiley

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