Ultrastable supported oxygen evolution electrocatalyst formed by ripening-induced embedding

The future deployment of terawatt-scale proton exchange membrane water electrolyzer (PEMWE) technology necessitates development of an efficient oxygen evolution catalyst with low cost and long lifetime. Currently, the stability of the most active iridium (Ir) catalysts is impaired by dissolution, redeposition, detachment, and agglomeration of Ir species. Here we present a ripening-induced embedding strategy that securely embeds the Ir catalyst in a cerium oxide support. Cryogenic electron tomography and all-atom kinetic Monte Carlo simulations reveal that synchronizing the growth rate of the support with the nucleation rate of Ir, regulated by sonication, is pivotal for successful synthesis. A PEMWE using this catalyst achieves a cell voltage of 1.72 volts at a current density of 3 amperes per square centimeter with an Ir loading of just 0.3 milligrams per square centimeter and a voltage degradation rate of 1.33 microvolts per hour, as demonstrated by a 6000-hour accelerated aging test.

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Publication Details

Journal
Science
Published
2025-02-13
DOI
https://doi.org/10.1126/science.adr3149
Citations
219
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
79.60
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article

Ultrastable supported oxygen evolution electrocatalyst formed by ripening-induced embedding

Qisheng Yan, Wenjuan Shi, Ke Xie, X Hu et al.
219 citations
Science
Electrocatalysts for Energy Conversion
79.60
article

Ultrastable supported oxygen evolution electrocatalyst formed by ripening-induced embedding

Qisheng Yan, Wenjuan Shi, Ke Xie, X Hu, Shuqing Fu, Yifei Xu, Xin Xu, Shiwen Cui, Chengkun Xing, Tonghao Shen, Liangyao Xue, Kai Sun, Wenzhe Niu, Sai Duan, Jingjing Li, Junfeng Chen, Yong Yang, Chenyang Wei, Bo Zhang, Xiao Yang, Ruijie Wang
article en
219 citations

Abstract

The future deployment of terawatt-scale proton exchange membrane water electrolyzer (PEMWE) technology necessitates development of an efficient oxygen evolution catalyst with low cost and long lifetime. Currently, the stability of the most active iridium (Ir) catalysts is impaired by dissolution, redeposition, detachment, and agglomeration of Ir species. Here we present a ripening-induced embedding strategy that securely embeds the Ir catalyst in a cerium oxide support. Cryogenic electron tomography and all-atom kinetic Monte Carlo simulations reveal that synchronizing the growth rate of the support with the nucleation rate of Ir, regulated by sonication, is pivotal for successful synthesis. A PEMWE using this catalyst achieves a cell voltage of 1.72 volts at a current density of 3 amperes per square centimeter with an Ir loading of just 0.3 milligrams per square centimeter and a voltage degradation rate of 1.33 microvolts per hour, as demonstrated by a 6000-hour accelerated aging test.

ScienceVol. 387(6735)
Northwestern University (US), Fudan University (CN), Hefei University (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN)
Clean water and sanitation
Openalex Percentile: Top 0%
Electrocatalysts for Energy Conversion
79.60
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