4.8 Article

A direct mechanochemical conversion of Pt-doped metal-organic framework-74 from doped metal oxides for CO oxidation

期刊

MATERIALS TODAY NANO
卷 17, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.mtnano.2021.100158

关键词

Metal-organic frameworks; Doping; Mechanochemical conversion; Mixed-metal metal-organic frameworks; CO oxidation

资金

  1. Science and Technology Commission of Shanghai Municipality [19YF1433300]
  2. ShanghaiTech University Startup Fund
  3. China Postdoctoral Science Foundation [2020M681343]
  4. Center for high-resolution electron microscopy (C-EM) [EM02161943]
  5. SPST, ShanghaiTech University
  6. Analytical Instrumentation Center [SPST-AIC10112914]

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Pt-doped Zn-MOF-74 was prepared through a mechanochemical conversion approach, showing potential as active sites for catalyzing CO oxidation reaction. This study provides a novel design strategy for the synthesis of mixed-metal metal-organic frameworks with extended functionalities.
Mixed-metal metal-organic frameworks (MM-MOFs) contain more than one type of metal node, which can improve or even introduce new features compared with the single metal frameworks. Traditionally, most of the MM-MOFs are synthesized by solution method which requires all the metal ions to form stable coordination with the ligand in a single framework and therefore limits the choice of the metal ions. In this work, Pt-doped Zn-MOF-74 (PtZn-MOF-74) has been prepared through a mechanochemical conversion approach from Pt-doped ZnO (Pt-ZnO) directly. The absence of a large quantity of solvent limits the solvation and diffusion of growth species during the mechanochemical conversion and therefore prevented the agglomeration of Pt dopants in PtZn-MOF-74. CO oxidation was used to evaluate the catalytic performance of the prepared MM-MOFs. Compared with inert Zn-MOF-74, PtZn-MOF-74 with unsaturated coordinated Pt at elevated temperature can act as the active sites to catalyze CO oxidation reaction. This study provides a novel design strategy for the synthesis of MM-MOFs with extended functionalities. (C) 2021 Elsevier Ltd. All rights reserved.

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