April 22 - 26, 2024
Seattle, Washington
May 7 - 9, 2024 (Virtual)
Symposium Supporters
2024 MRS Spring Meeting
EN09.11.03

Electrochemical Activity of Iridium Oxides for OER: Porosity, Crystallinity and Nanocages

When and Where

Apr 25, 2024
2:00pm - 2:30pm
Room 337, Level 3, Summit

Presenter(s)

Co-Author(s)

Cédric Tard1,Silvia Duran1,Marine Elmaalouf2,Andrea Zitolo3,Benedikt Lassalle3,Cédric Boissière4,Marco Faustini4,Marion Giraud2,Jennifer Peron2

Ecole Polytechnique1,Université Paris-Cité2,Synchrotron Soleil3,Sorbonne Université4

Abstract

Cédric Tard1,Silvia Duran1,Marine Elmaalouf2,Andrea Zitolo3,Benedikt Lassalle3,Cédric Boissière4,Marco Faustini4,Marion Giraud2,Jennifer Peron2

Ecole Polytechnique1,Université Paris-Cité2,Synchrotron Soleil3,Sorbonne Université4
Iridium oxide is still considered the superior material for the oxygen evolution reaction (OER) in acidic environment, as it maintains both high activity and stability, making it the benchmark material for green hydrogen production.<sup>[1]</sup> Despite the numerous studies describing the activity of IrO<sub>2</sub> materials for the OER, it is crucial to have a thorough understanding of its functional principles in order to optimize and rationalize its utilization. Towards this objective, we have been able to produce porous iridium-based mixed oxides using aerosol chemistry via a sol-gel process,<sup>[2]</sup> to decouple the electronic processes from the structural transformations.<sup>[3]</sup> Indeed, the oxidation of iridium from IrO<sub>2</sub> occurs upon calcination, but is not related to the crystallization of the material itself. The measurements demonstrate that short-range ordering, corresponding to sub-2nm crystal size, is controlling the activity of the materials. This is the case regardless of the initial oxidation state and composition of the calcined iridium oxides, as evidenced by XAS, XRD and XPS measurements. Regarding other types of porous materials, we have also been able to prepare hierarchical structures of IrO<sub>2</sub> based on Pearson’s hard and soft acid-base theory and characterize their outstanding activity toward the OER.<sup>[4]</sup><br/><br/>[1] Chatenet, M. <i>et al., Chem. Soc. Rev</i>. <b>2022</b>,<i>51</i>, 4583-4762.<br/>[2] a) Faustini, M. <i>et al.,</i> <i>Adv. Energy Mater.</i> <b>2019</b>, <i>9</i>, 1802136; b) Duran, S. <i>et al., ChemElectroChem</i> <b>2021</b>, <i>8</i>, 3519-3524.<br/>[3] Elmaalouf, M. <i>et al., Nat. Commun. </i><b>2021</b>, <i>12</i>, 3935.<br/>[4] Elmaalouf, M. <i>et al., Chem. Sci.</i> <b>2022</b>, <i>13</i>, 11807-11816.

Keywords

extended x-ray absorption fine structure (EXAFS) | Ir

Symposium Organizers

Christopher Barile, University of Nevada, Reno
Nathalie Herlin-Boime, CEA Saclay
Michel Trudeau, Concordia University
Edmund Chun Ming Tse, University Hong Kong

Session Chairs

Sophie Cassaignon
Sandrine Lyonnard

In this Session