Mesoporous Amorphous High-Entropy Oxide Films: Unlocking Enhanced Redox Activity

High-entropy oxides (HEOs) represent a frontier in catalyst design via entropy-stabilized solid solution formation. However, their catalytic efficiency is limited by their bulk and dense nature. This work presents a strategic approach to tackle this challenge by fabricating mesoporous amorphous HEO films (MA-HEOF) possessing maximized active site utilization efficiency. The success hinges on the as-developed geometric engineering strategy via controlled deposition–precipitation to confine the amorphous HEO thin film on the surface of mesoporous channels. The unique structure of MA-HEOF was elucidated via microscopy-, X-ray-, and neutron-based techniques, which were manifested by enriched surface-activated lattice oxygen and enhanced redox activity, as confirmed by isotope studies. Besides, the MA-HEOF could stabilize and modulate the properties of integrated noble metal sites, enhancing their redox activity in diverse reactions. The approaches and insights presented herein provide guidance on maximizing the utilization efficiency of high-entropy materials in catalysis and beyond.

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Publication Details

Journal
ACS Catalysis
Published
2025-06-24
DOI
https://doi.org/10.1021/acscatal.5c01591
Citations
4
Primary Topic
Transition Metal Oxide Nanomaterials
Type
article
Field-Weighted Citation Impact
2.43

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article

Mesoporous Amorphous High-Entropy Oxide Films: Unlocking Enhanced Redox Activity

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4 citations
ACS Catalysis
Transition Metal Oxide Nanomaterials
2.43
article

Mesoporous Amorphous High-Entropy Oxide Films: Unlocking Enhanced Redox Activity

Kevin M. Siniard, Felipe Polo‐Garzon, Sheng Dai, Darren M. Driscoll, Shize Yang, Austin Houston, Gerd Duscher, Alexander S. Ivanov, Junyan Zhang, Jue Liu, Meijia Li, Qingju Wang, Zhenzhen Yang
article en
4 citations

Abstract

High-entropy oxides (HEOs) represent a frontier in catalyst design via entropy-stabilized solid solution formation. However, their catalytic efficiency is limited by their bulk and dense nature. This work presents a strategic approach to tackle this challenge by fabricating mesoporous amorphous HEO films (MA-HEOF) possessing maximized active site utilization efficiency. The success hinges on the as-developed geometric engineering strategy via controlled deposition–precipitation to confine the amorphous HEO thin film on the surface of mesoporous channels. The unique structure of MA-HEOF was elucidated via microscopy-, X-ray-, and neutron-based techniques, which were manifested by enriched surface-activated lattice oxygen and enhanced redox activity, as confirmed by isotope studies. Besides, the MA-HEOF could stabilize and modulate the properties of integrated noble metal sites, enhancing their redox activity in diverse reactions. The approaches and insights presented herein provide guidance on maximizing the utilization efficiency of high-entropy materials in catalysis and beyond.

ACS CatalysisVol. 15(13)
Oak Ridge National Laboratory (US), Yale University (US), NOAA Chemical Sciences Laboratory (US), University of Tennessee at Knoxville (US)
Basic Energy Sciences
Openalex Percentile: Top 11%
Transition Metal Oxide Nanomaterials
2.43
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