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Solvent-Free Photoreduction of CO2 to CO Catalyzed by Fe-MOFs with Superior Selectivity.

Xiao-Yao DaoJin-Han GuoYuan-Ping WeiFan GuoYi LiuWei-Yin Sun
Published in: Inorganic chemistry (2019)
It is deemed as a desired approach to utilize solar energy for the conversion of CO2 into valuable products, and the majority of the MOFs-based photocatalytic reductions of CO2 have focused on formic acid (HCOOH) production with an organic solvent as the reaction medium. Herein, we report a solvent-free reaction route for the photoreduction of CO2 catalyzed by Fe-MOFs, namely, NH2-MIL-53(Fe) [(Fe(OH)(NH2-BDC)]•G, NH2-MIL-88B(Fe) [Fe3O(H2O)3(NH2-BDC)3]Cl•G, and NH2-MIL-101(Fe) [Fe3O(H2O)3(NH2-BDC)3]Cl•G (NH2-BDC = 2-aminoterephthalic acid; G = guest and/or solvent molecules). Compared with the orthodox reaction route, the present out-of-the-way photocatalytic reduction of CO2 with superior selectivity to CO occurs at the gas-solid interface. The reaction procedure is environmentally friendly and provides a possibility to address the CO2 emission problem. Importantly, NH2-MIL-101(Fe) shows the highest photocatalytic activity among these Fe-MOFs due to its efficient charge separation and electron transfer.
Keyphrases
  • metal organic framework
  • room temperature
  • ionic liquid
  • electron transfer
  • visible light
  • perovskite solar cells
  • highly efficient
  • gold nanoparticles
  • mass spectrometry
  • high resolution
  • water soluble