The Impact of Metal Centers in the M-MOF-74 Series on Formic Acid Production

Dominika O. Wasik, José Manuel Vicent-Luna (Corresponding author), Shima Rezaie, Azahara Luna-Triguero, Thijs J.H. Vlugt, Sofía Calero (Corresponding author)

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Abstract

The confinement effect of porous materials on the thermodynamical equilibrium of the CO2 hydrogenation reaction presents a cost-effective alternative to transition metal catalysts. In metal-organic frameworks, the type of metal center has a greater impact on the enhancement of formic acid production than the scale of confinement resulting from the pore size. The M-MOF-74 series enables a comprehensive study of how different metal centers affect HCOOH production, minimizing the effect of pore size. In this work, molecular simulations were used to analyze the adsorption of HCOOH and the CO2 hydrogenation reaction in M-MOF-74, where M = Ni, Cu, Co, Fe, Mn, Zn. We combine classical simulations and density functional theory calculations to gain insights into the mechanisms that govern the low coverage adsorption of HCOOH in the surrounding of the metal centers of M-MOF-74. The impact of metal centers on the HCOOH yield was assessed by Monte Carlo simulations in the grand-canonical ensemble, using gas-phase compositions of CO2, H2, and HCOOH at chemical equilibrium at 298.15-800 K, 1-60 bar. The performance of M-MOF-74 in HCOOH production follows the same order as the uptake and the heat of HCOOH adsorption: Ni > Co > Fe > Mn > Zn > Cu. Ni-MOF-74 increases the mole fraction of HCOOH by ca. 105 times compared to the gas phase at 298.15 K, 60 bar. Ni-MOF-74 has the potential to be more economically attractive for CO2 conversion than transition metal catalysts, achieving HCOOH production at concentrations comparable to the highest formate levels reported for transition metal catalysts and offering a more valuable molecular form of the product.

Original languageEnglish
Pages (from-to)45006-45019
Number of pages14
JournalACS Applied Materials and Interfaces
Volume16
Issue number34
DOIs
Publication statusPublished - 28 Aug 2024

Keywords

  • adsorption
  • hydrogenation
  • metal−organic frameworks
  • molecular simulations
  • thermodynamic equilibrium

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