4.8 Article

A Principle for Highly Active Metal Oxide Catalysts via NaCl-Based Solid Solution

Journal

CHEM
Volume 6, Issue 7, Pages 1723-1741

Publisher

CELL PRESS
DOI: 10.1016/j.chempr.2020.04.003

Keywords

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Funding

  1. National Natural Science Foundation of China [21776174]
  2. Thousand Talent Program
  3. Open Foundation of the State Key Laboratory of Ocean Engineering (Shanghai Jiao Tong University of China) [1809]
  4. Shanghai Jiao Tong University Scientific and Technological Innovation Funds [2019QYB06]
  5. China Shipbuilding Industry Corporation (CSIC)
  6. Zhejiang Xinan Chemical Industrial Group
  7. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, geosciences, and Biosciences Division, Catalysis Science program

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Toward the preparation of industrial metal oxide catalysts, sacrificial organic templates, excessive solvents, complex impregnation, and drying steps are generally required. Here, we report a versatile rule for the simple synthesis of highly porous metal oxides with well. dispersed noble metal species. Porous metal oxides (Co3O4, Fe-x, O-y, and Cr2O3) are obtained with some surface areas (e.g., Cr2O3: 224 m(2) g(-1)) beyond the record value. Surprisingly, small noble metal nanoparticles (e.g., Pd: 3.1 and Pt: 3.2 nm) could be incorporated by this solid-state process simultaneously. Corresponding Rh-Co3O4, Pd-FexOy, and Pt-Cr2O3 exhibit excellent performance: CH4 combustion (T-90 = similar to 360 degrees C and thermal stability: >100 h at 680 degrees C), hydrogenation of nitrobenzene and derivatives (turnover number [TON] = 2.49 x 10(4), 300 mmol per run), and reversed water gas shift (RWGS) reaction (44% CO2 conversion with similar to 98% CO selectivity and thermal stability: >100 h at 500 degrees C), respectively. Therefore, current principle via a NaCI-based solid solution could provide a solid-state, fast, and efficient route for processing metal oxide catalysts.

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