Looping metal-support interaction in heterogeneous catalysts during redox reactions

Metal-support interfaces fundamentally govern the catalytic performance of heterogeneous systems through complex interactions. Here, utilizing operando transmission electron microscopy, we uncover a looping metal-support interaction in NiFe-Fe<sub>3</sub>O<sub>4</sub> catalysts during the hydrogen oxidation reaction. At the NiFe-Fe<sub>3</sub>O<sub>4</sub> interfaces, lattice oxygens react with NiFe-activated H atoms, gradually sacrificing themselves and resulting in dynamically migrating interfaces. Meanwhile, reduced iron atoms migrate to the {111} surface of Fe<sub>3</sub>O<sub>4</sub> support and react with oxygen molecules. Consequently, the hydrogen oxidation reaction separates spatially on a single nanoparticle and is intrinsically coupled with the redox reaction of the Fe<sub>3</sub>O<sub>4</sub> support through the dynamic migration of metal-support interfaces. Our work provides previously unidentified mechanistic insight into metal-support interactions and underscores the transformative potential of operando methodologies for studying atomic-scale dynamics.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-09-29
DOI
https://doi.org/10.1038/s41467-025-63646-1
Citations
4
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
2.07

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Looping metal-support interaction in heterogeneous catalysts during redox reactions

Liang Zhang, Lin Gu, Jianxiong Zhao, Shiyu Zhen et al.
4 citations
Nature Communications
Catalytic Processes in Materials Science
2.07
article

Looping metal-support interaction in heterogeneous catalysts during redox reactions

Liang Zhang, Lin Gu, Jianxiong Zhao, Shiyu Zhen, Dong Su, Mengshu Ge, Dan Zhou, Xiaozhi Liu, Yue Pan
article en
4 citations

Abstract

Metal-support interfaces fundamentally govern the catalytic performance of heterogeneous systems through complex interactions. Here, utilizing operando transmission electron microscopy, we uncover a looping metal-support interaction in NiFe-Fe<sub>3</sub>O<sub>4</sub> catalysts during the hydrogen oxidation reaction. At the NiFe-Fe<sub>3</sub>O<sub>4</sub> interfaces, lattice oxygens react with NiFe-activated H atoms, gradually sacrificing themselves and resulting in dynamically migrating interfaces. Meanwhile, reduced iron atoms migrate to the {111} surface of Fe<sub>3</sub>O<sub>4</sub> support and react with oxygen molecules. Consequently, the hydrogen oxidation reaction separates spatially on a single nanoparticle and is intrinsically coupled with the redox reaction of the Fe<sub>3</sub>O<sub>4</sub> support through the dynamic migration of metal-support interfaces. Our work provides previously unidentified mechanistic insight into metal-support interactions and underscores the transformative potential of operando methodologies for studying atomic-scale dynamics.

Nature CommunicationsVol. 16(1)
Chinese Academy of Sciences (CN), Denssolutions (Netherlands) (NL), FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ), Leibniz Institute for Crystal Growth (DE), Institute of Physics (CN), National Laboratory for Superconductivity (CN), University of Chinese Academy of Sciences (CN), Tsinghua University (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, China Postdoctoral Science Foundation
Openalex Percentile: Top 12%
Catalytic Processes in Materials Science
2.07
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.