4.8 Article

A High Entropy Oxide Designed to Catalyze CO Oxidation Without Precious Metals

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 7, Pages 8120-8128

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c17446

Keywords

high entropy; ceramics; oxide; nanomaterial; CO oxidation; catalysis

Funding

  1. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Advanced Manufacturing Office [DE-LC 000L059]
  2. Laboratory Directed Research and Development program at Sandia National Laboratories
  3. U.S. DOE's National Nuclear Security Administration [DE-NA0003525]

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This study demonstrates the application of high entropy oxides (HEOs) in designing efficient oxidation catalysts with enhanced catalytic activity, oxygen storage capacity, and thermal stability. Through a simple sol-gel method, nanostructured HEOs with high surface areas up to 138m(2)/g were synthesized, marking a significant structural improvement.
The chemical complexity of single-phase multicationic oxides, commonly termed high entropy oxides (HEOs), enables the integration of conventionally incompatible metal cations into a single-crystalline phase. However, few studies have effectively leveraged the multicationic nature of HEOs for optimization of disparate physical and chemical properties. Here, we apply the HEO concept to design robust oxidation catalysts in which multicationic oxide composition is tailored to simultaneously achieve catalytic activity, oxygen storage capacity, and thermal stability. Unlike conventional catalysts, HEOs maintain single-phase structure, even at high temperature, and do not rely on the addition of expensive platinum group metals (PGM) to be active. The HEOs are synthesized through a facile, relatively low temperature (500 degrees C) sol-gel method, which avoids excessive sintering and catalyst deactivation. Nanostructured high entropy oxides with surface areas as high as 138 m(2)/g are produced, marking a significant structural improvement over previously reported HEOs. Each HEO contained Ce in varying concentrations, as well as four other metals among Al, Fe, La, Mn, Nd, Pr, Sm, Y, and Zr. All samples adopted a fluorite structure. First row transition metal cations were most effective at improving CO oxidation activity, but their incorporation reduced thermal stability. Rare earth cations were necessary to prevent thermal deactivation while maintaining activity. In sum, our work demonstrates the utility of entropy in complex oxide design and a low-energy synthetic route to produce nanostructured HEOs with cations selected for a cooperative effect toward robust performance in chemically and physically demanding applications.

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