4.6 Article

Probing growth of metal-organic frameworks with X-ray scattering and vibrational spectroscopy

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 24, Issue 42, Pages 26102-26110

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cp04375k

Keywords

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Funding

  1. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy through the Condensed Phase, Interfaces and Molecular Sciences Program, Chemical Sciences Division [DE-AC02-05CH11231]
  2. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy through the Gas Phase Chemical Physics Program
  3. U.S. Department of Energy Office of Basic Energy Sciences [DE-SC0019992]
  4. Arnold O. Beckman Postdoctoral Fellowship
  5. U.S. Department of Energy (DOE) [DE-SC0019992] Funding Source: U.S. Department of Energy (DOE)

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This study investigated the crystallization and growth mechanism of the metal-organic framework Co-MOF-74 within microscopic volumes using wide-angle X-ray scattering and vibrational spectroscopy. The experiments revealed the molecular and structural details of the growth process, and the reduction in reagent volume in the microchip reactor accelerated the reaction rate. The synthesis of the metal-organic framework in microscopic volumes resulted in monodisperse and micron-sized crystals, which differed from those typically observed under bulk reaction conditions.
Nucleation and crystallization arising from liquid to solid phase are involved in a multitude of processes in fields ranging from materials science to biology. Controlling the thermodynamics and kinetics of growth is advantageous to help tune the formation of complex morphologies. Here, we harness wide-angle X-ray scattering and vibrational spectroscopy to elucidate the mechanism for crystallization and growth of the metal-organic framework Co-MOF-74 within microscopic volumes enclosed in a capillary and an attenuated total reflection microchip reactor. The experiments reveal molecular and structural details of the growth processes, while the results of plane wave density functional calculations allow identification of lattice and linker modes in the formed crystals. Synthesis of the metal-organic framework with microscopic volumes leads to monodisperse and micron-sized crystals, in contrast to those typically observed under bulk reaction conditions. Reduction in the volume of reagents within the microchip reactor was found to accelerate the reaction rate. The coupling of spectroscopy with scattering to probe reactions in microscopic volumes promises to be a useful tool in the synthetic chemist's kit to understand chemical bonding and has potential in designing complex materials.

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