Spin enhanced oxygen evolution reaction: effects of chirality and magnetic fields.
Priscila Vensaus a b c d, Yunchang Liang a b, Nicolas Zigon e, Jean-Phillipe Ansermet b, Galo J. A. A. Soler-Illia c, Narcis Avarvari e, 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 Instituto de Nanosistemas, Universidad Nacional de San Martín, Argentina, Argentina
d Laboratory of Nanoscience for Energy Technologies (LNET), STI, École Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland
e MOLTECH-Anjou
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Fall 2024 Conference (MATSUSFall24)
#ChiNano - Exploring Chiral Nanostructured Materials and Plasmonics for Energy applications
Lausanne, Switzerland, 2024 November 12th - 15th
Organizers: Sascha Feldmann, Magalí Lingenfelder and Giulia Tagliabue
Oral, Priscila Vensaus, presentation 236
DOI: https://doi.org/10.29363/nanoge.matsusfall.2024.236
Publication date: 28th August 2024

The oxygen evolution reaction (OER, 1) is critical for hydrogen production via water electrolysis. However, it has notably sluggish kinetics. It has been proposed that part of the high overpotential required for oxygen formation is due to the spin restrictions necessary for oxygen formation in its fundamental triplet state [1].

 4 OH- → O2 + 2 H2O + 4 e-            Eº=1.23 V            (1)

We investigated how spin alignment can enhance the OER and reduce the competing water oxidation reaction that forms H2O2. Specifically, we explored enhancing the OER by modifying state-of-the-art electrodes with chiral molecules, leveraging the chiral-induced spin selectivity (CISS) effect [2,3]. By comparing the electrocatalytic performance of electrodes modified with different compositions of chiral molecules, we found that the OER enhancement is significantly influenced by the presence of homochiral domains. Furthermore, we confirmed the spin-selectivity effect by observing a reduction in H2O2 formation on mesoporous hybrid systems.[4] Additionally, we studied the impact of static magnetic fields on reaction kinetics and mass transport using key electrocatalysts.[5] Our findings offer a strategy to optimize spin-enhanced OER, which can be easily extended to boost multiple key electrocatalytic reactions that involve spin selective intermediates.

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