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January 13, 2024CCS Chemistry97 citationsOpen Access

High-Porosity, Layered Iridium Oxide as an Efficient, Durable Anode Catalyst for Water Splitting

ZXZhoubing XieXLXiao LiangZKZhenye Kang

Key Points

  • Synthesize a highly porous, layered iridium oxide catalyst to reduce iridium loading while maintaining high activity and durability in proton exchange membrane water electrolyzers.
  • Synthesized porous layered iridium oxide microparticles (p-L-IrO2) via low-temperature alkali metal salt templating followed by acid treatment.
  • Fabricated low-loading anode catalytic layers and evaluated performance in a proton exchange membrane water electrolyzer using a Nafion N115 membrane at 80 °C.
  • The p-L-IrO2 catalyst exhibited approximately 74% open porosity, exposing a high density of active hydroxylated edge sites operating through an adsorbate evolution mechanism.
  • Achieved an electrolyzer performance of 2.7 A cm⁻² at 1.9 V at 80 °C by simultaneously mitigating activation and mass transport losses.
  • Demonstrated extended catalytic stability, retaining activity for 2,300 hours at a constant current density of 1.0 A cm⁻².

Abstract

Lowering iridium (Ir) loading without sacrificing activity and durability is critical to the future development of proton exchange membrane water electrolyzer (PEMWE). Here, we present the synthesis of iridate-derived, layered iridium oxide microparticles (dubbed p-L-IrO2) with a high open porosity of approximately 74% and their structural advantages for the fabrication of efficient, durable, low-Ir-loading anode catalytic layer in PEMWE. The p-L-IrO2 material is synthesized by an easily scalable route involving acid treatment of alkali metal salt-templated iridates that form in mixed alkali metal nitrates-hydroxides at low temperature. The combination of high-porosity morphology and layered structure in the material preferentially exposes a high density of hydroxylated edge sites, which are catalytically active and stable to achieve the oxygen evolution reaction via a structurally hydroxyl group-participated adsorbate evolution mechanism. This material is further demonstrated to enable the fabrication of low-Ir-loading anode catalytic layers in PEMWE, which can afford excellent catalytic performance (2.7 A cm-2@1.9 V@80 °C; membrane: Nafion™ N115) due to the simultaneous reduction of activation and mass transport losses and retention of catalytic activity for 2300 h at 1.0 A cm-2 current density. © 2024 Chinese Chemical Society.

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Cite This Study

Xie et al. (2024) studied this question.

synapsesocial.com/papers/69d6d02b8dca315383ed9248https://doi.org/10.31635/ccschem.024.202303586
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