Magnetic Enhancement of Electrocatalysis: Universality and Limitations
Yunchang Liang a b, Priscila Vensaus a b, Felipe A. Garcés-Pineda c, Jean-Philippe Ansermet b, José R. Galan-Mascaros c d, Magalí Lingenfelder a b
a Max Planck-EPFL Laboratory for Molecular Nanoscience and Technology, École Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland
b Institut of Physics (IPHYS), Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland
c Institute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology (BIST), Av. Països Catalans 16, E-43007 Tarragona, Spain
d Catalan Institution for Research and Advanced Studies (ICREA), Passeig Lluis Com- panys, 23, Barcelona 08010, Spain
Materials for Sustainable Development Conference (MATSUS)
Proceedings of nanoGe Spring Meeting 2022 (NSM22)
#ElectroCat22. Electrocatalysis for the Production of Fuels and Chemicals
Online, Spain, 2022 March 7th - 11th
Organizers: Julio Lloret Fillol and James Durrant
Contributed talk, Yunchang Liang, presentation 195
DOI: https://doi.org/10.29363/nanoge.nsm.2022.195
Publication date: 7th February 2022

A carbon-neutral and sustainable future requires advanced electrocatalysis systems[1]. Magnetism-induced enhancement of electrocatalytic reactions has been gaining increasing attention [2],[3],[4]. A simple and efficient way to achieve an enhancement is to apply an external magnetic field to the reaction[5]. Various mechanisms concerning different aspects of the reactions, e.g., reaction kinetics[5],[6] and mass transfer processes[7], have been introduced. However, the enhancement is likely a result of a synergistic effect of at least two mechanisms. Here, using key electrocatalytic reactions, i.e., oxygen evolution reaction (OER), oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER), and homogeneous magnetic fields provided by an electromagnet, we demonstrate the importance of experimentally decoupling the mechanisms affecting the electrocatalytic reactions at electrodes with different magnetic properties. Our results show that the effect on the reaction kinetics and selectivity is exclusive to ferromagnetic catalysts and electron spin-dependent reactions under sufficient magnetic field strength; however, an enhancement of the mass transfer is universal. We provide a versatile strategy to optimize the magnetic enhancement that can be implemented to boost electrocatalytic reactions.

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