Precision Structure Engineering of High-Entropy Oxides under Ambient Conditions
High-entropy oxides (HEOs) have unveiled a unique frontier in the realm of heterogeneous catalysis, taking advantage of the entropic effect and increased complexities to deliver ultrahigh stability and large tuning capability. However, current HEO synthesis mainly relies on high-temperature annealing approaches affording HEOs possessing no or low surface area, inferior active site exposure efficiency, and low controllability over the structure tuning. The grand challenge lies in producing high-quality HEO catalysts with high active site utilization efficiency, which relies on precision structure engineering, preferably under mild conditions. In this work, an in situ lattice engineering approach was developed to afford a supported HEO catalyst under ambient conditions. The HEO compositions (CuCoFeNiMnOx) were uniformly integrated into the lattice of CeO2 driven by cavitation-induced nucleation being generated via ultrasonication. The as-afforded catalysts were featured by high surface area, atomically dispersed HEO compositions, active redox properties, abundant oxygen vacancies (OV), antiagglomeration, and high phase stability under harsh conditions. Compared with the ex situ introduction of HEO on the surface, the in situ method provides dual benefits to maintain the dispersity of HEO via entropic and lattice confinement effects. Engineering the complex HEO within the lattice of fluorite-structured CeO2 also yields abundant defects (e.g., OV) and active metal sites with strong reducing properties (e.g., Ce3+ and Cu+), which greatly improves the activity of the lattice oxygen and tunability of the adsorption behavior of the guest molecules, especially in the presence of impurities (e.g., water and propane). The catalytic performance of the supported HEO catalyst in oxidative procedures surpasses the pure dense phase HEO as well as the ex situ-generated catalysts. The synthesis approach being developed in this work, together with the fundamental understanding in structure evolution and reaction mechanism, showcases a facile pathway under ambient conditions to generate stable catalysts capable of maintaining structural robustness in high-temperature conditions while delivering enhanced catalytic performance.
Authors
- Kevin M. Siniard (ORCID: https://orcid.org/0000-0003-0241-9705)
- Felipe Polo‐Garzon (ORCID: https://orcid.org/0000-0002-6507-6183)
- Sheng Dai (ORCID: https://orcid.org/0000-0002-8046-3931)
- Darren M. Driscoll
- Xinhui Lu (ORCID: https://orcid.org/0000-0002-1908-3294)
- Zili Wu (ORCID: https://orcid.org/0000-0002-4468-3240)
- Alexander S. Ivanov (ORCID: https://orcid.org/0000-0002-8193-6673)
- Hao Chen (ORCID: https://orcid.org/0000-0002-6658-4198)
- Yuanyuan Li (ORCID: https://orcid.org/0000-0003-3074-9672)
- Meijia Li (ORCID: https://orcid.org/0000-0002-6113-7428)
- Yandi Cai
- Junyan Zhang
- Zhenzhen Yang
Institutions
- Oak Ridge National Laboratory (US)
- Hunan University (CN)
- State Key Laboratory of Pollution Control and Resource Reuse (CN)
- University of Tennessee at Knoxville (US)
- Nanjing University (CN)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2024-09-23
- DOI
- https://doi.org/10.1021/acscatal.4c03349
- Citations
- 12
- Primary Topic
- Catalysis and Oxidation Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.28
Funders
- Chemical Sciences, Geosciences, and Biosciences Division