4.8 Article

Defect-Rich High-Entropy Oxide Nanosheets for Efficient 5-Hydroxymethylfurfural Electrooxidation

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 37, 页码 20253-20258

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202107390

关键词

biomass upgrading; defect chemistry; electrocatalysis; high-entropy oxides; plasma technology

资金

  1. national key R&D program of china [2020YFA0710000]
  2. National Natural Science Foundation of China [21701043, 22002039, 21825201, U19A2017]
  3. Provincial Natural Science Foundation of Hunan [2019GK2031]
  4. China Postdoctoral Science Foundation [2020M682549, 2020M682541, 2020M682542, 2020M672473]
  5. Science and Technology Innovation Program of Hunan Province, China [2020RC2020, 2020RC2023]
  6. Changsha Municipal Natural Science Foundation [kq2007009]

向作者/读者索取更多资源

A low-temperature plasma strategy was used to prepare defect-rich HEOs nanosheets with high surface area, which showed improved catalytic activity for organic compound oxidation and outperformed HEOs prepared by high-temperature methods. This method provides new opportunities for synthesizing nanostructured HEOs with great potential applications.
High-entropy oxides (HEOs), a new concept of entropy stabilization, exhibit unique structures and fascinating properties, and are thus important class of materials with significant technological potential. However, the conventional high-temperature synthesis techniques tend to afford micron-scale HEOs with low surface area, and the catalytic activity of available HEOs is still far from satisfactory because of their limited exposed active sites and poor intrinsic activity. Here we report a low-temperature plasma strategy for preparing defect-rich HEOs nanosheets with high surface area, and for the first time employ them for 5-hydroxymethylfurfural (HMF) electrooxidation. Owing to the nanosheets structure, abundant oxygen vacancies, and high surface area, the quinary (FeCrCoNiCu)(3)O-4 nanosheets deliver improved activity for HMF oxidation with lower onset potential and faster kinetics, outperforming that of HEOs prepared by high-temperature method. Our method opens new opportunities for synthesizing nanostructured HEOs with great potential applications.

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