4.6 Article

Creating Coordination Mismatch in MOFs: Tuning from Pore Structure of the Derived Supported Catalysts to Their Catalytic Performance

Journal

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 58, Issue 14, Pages 5543-5551

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.9b01096

Keywords

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Funding

  1. National Natural Science Foundation of China [21636010, 21878342]
  2. China Postdoctoral Science Foundation [2018M643001]
  3. Hunan Provincial Natural Science Foundation of China [2019JJ50758]
  4. Postdoctoral Science Foundation of Central South University [205440]
  5. Key Laboratory of Photochemical Conversion and Optoelectronic Materials [PCOM201816]
  6. TIPC, CAS, Beijing, China
  7. State Key Laboratory of Powder Metallurgy, Central South University, Changsha, China
  8. Fundamental Research Funds for Central Universities of Central South University [2018zzts114]

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Hollow porous carbon (HPC) composed of inner voids and outer shells, is receiving increasing attention in constructing supported catalysts for diverse applications. It is of great allure but still challenging to controllably tune the secondary porous structure (pore in the outer shells) of the HPC support to improve the performance of the catalysts. Herein, a Ni-substituted ZIF-67 was used as a precursor to prepare HPC-supported catalysts. We found that Ni2+ can partially substitute Co2+ to create defected structure within ZIF-67, and the secondary pore structure of the derived HPC can be facilely tuned by adjusting the ratio of Ni2+ to Co2+. Catalyst HPC-Ni-ZIF-1 with hierarchical secondary pore and the largest pore volume exhibits an excellent catalytic performance for the hydrogenation of nitro compounds to corresponding amino compounds.

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