Synergistic Ni Single Atoms/Nanoparticles on CeO <sub>2</sub> for High‐Performance and Durable SOFC Hydrogen Electrodes

ABSTRACT Degradation of the three‐phase boundaries in Ni‐based anodes at high operating temperature compromises hydrogen oxidation reaction catalytic activity and shortens the lifespan of solid oxide fuel cells. Herein, an oxide‐based anode decorated with Ni single atoms (SAs) and nanoparticles (NPs), i.e., e‐Ni/CeO 2 –5%, is synthesized by combining engineering of UiO‐66(Ce) metal organic frameworks (MOFs) and exsolution, where (i) Ni SAs donate electrons to generate oxygen vacancies and stabilize Ni NPs, (ii) NPs dissociate H 2 to facilitate hydrogen spillover, and (iii) the abundant mesoporous channels in CeO 2 inherited from the unique MOFs structure enables high‐efficient mass transfer. Synergy of the above merits finally delivers a greatly improved peak power density of 1.46 W cm −2 at 800°C among oxide‐based anodes, exhibits remarkable durability with negligible voltage degradation (&lt; 0.005% h −1 ) over 500 h.

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Publication Details

Journal
Advanced Science
Published
2026-06-30
DOI
https://doi.org/10.1002/advs.76282
Primary Topic
Advancements in Solid Oxide Fuel Cells
Type
article
Field-Weighted Citation Impact
0.00

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Synergistic Ni Single Atoms/Nanoparticles on CeO 2 for High‐Performance and Durable SOFC Hydrogen Electrodes

Qian Yang, Yi Shen, Li Li, Fengyang Yu et al.
Advanced Science
Advancements in Solid Oxide Fuel Cells
article

Synergistic Ni Single Atoms/Nanoparticles on CeO 2 for High‐Performance and Durable SOFC Hydrogen Electrodes

Qian Yang, Yi Shen, Li Li, Fengyang Yu, Mengting Liu, Ling Huang
article en

Abstract

ABSTRACT Degradation of the three‐phase boundaries in Ni‐based anodes at high operating temperature compromises hydrogen oxidation reaction catalytic activity and shortens the lifespan of solid oxide fuel cells. Herein, an oxide‐based anode decorated with Ni single atoms (SAs) and nanoparticles (NPs), i.e., e‐Ni/CeO 2 –5%, is synthesized by combining engineering of UiO‐66(Ce) metal organic frameworks (MOFs) and exsolution, where (i) Ni SAs donate electrons to generate oxygen vacancies and stabilize Ni NPs, (ii) NPs dissociate H 2 to facilitate hydrogen spillover, and (iii) the abundant mesoporous channels in CeO 2 inherited from the unique MOFs structure enables high‐efficient mass transfer. Synergy of the above merits finally delivers a greatly improved peak power density of 1.46 W cm −2 at 800°C among oxide‐based anodes, exhibits remarkable durability with negligible voltage degradation (&lt; 0.005% h −1 ) over 500 h.

Advanced Science
Nanjing Tech University (CN), Xinjiang University (CN)
National Natural Science Foundation of China
Responsible consumption and production
Openalex Percentile: Top 17%
Advancements in Solid Oxide Fuel Cells
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