Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 14807-14818 |
| Number of pages | 12 |
| Journal | ACS Catalysis |
| Volume | 14 |
| Issue number | 19 |
| DOIs | |
| State | Published - Oct 4 2024 |
Funding
The research was supported financially by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science Program. Use of the NSLS-II (NIST beamline 6-BM and the 28-ID-1 beamline) was supported by the Department of Energy Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory (BNL) under contract no. DE-SC0012704. D.M.D. and A.S.I. thank Dr. Ravel and Dr. Kwon of BNL for their help during synchrotron experiments. The UV Raman measurement of this research was conducted at the Center for Nanophase Material Sciences (CNMS), which is a U.S. Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. The research was supported financially by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science Program.
Keywords
- CO oxidation
- ambient condition synthesis
- heterogeneous catalysis
- high-entropy oxides
- ultrasonication