4.6 Article

Anisotropic Band-Edge Absorption of Millimeter-Sized Zn(3-ptz)2 Single-Crystal Metal-Organic Frameworks

Journal

ACS OMEGA
Volume 7, Issue 28, Pages 24432-24437

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.2c01856

Keywords

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Funding

  1. ANID [1181743]
  2. DICYT-USACH [POSTDOC 041831HU]
  3. ANID Millennium Science Initiative Program [ICN17-012]
  4. NLHPC at Universidad de Chile [ECM-02]

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Metal-organic frameworks (MOFs) have shown promise for developing next-generation solid-state devices with applications in optics. However, the difficulty in growing large, high-quality MOF single crystals has hindered the implementation of functional devices. By controlling the synthesis conditions, researchers successfully produced large, noncentrosymmetric MOF single crystals with a unique shape and high surface area. These crystals exhibited anisotropic absorption, and the observed size dependence in optical anisotropy was correlated with the preferred orientation of the molecules. This work opens up possibilities for developing optical polarization switches based on MOFs.
Metal-organic frameworks (MOFs) have emerged as promising tailor-designed materials for developing next-generation solid-state devices with applications in linear and nonlinear coherent optics. However, the implementation of functional devices is challenged by the notoriously difficult process of growing large MOF single crystals of high optical quality. By controlling the solvothermal synthesis conditions, we succeeded in producing large individual single crystals of the noncentrosymmetric MOF Zn(3-ptz)(2) (MIRO-101) with a deformed octahedron habit and surface areas of up to 37 (mm)(2). We measured the UV-vis absorption spectrum of individual Zn(3-ptz)(2) single crystals across different lateral incidence planes. Millimeter-sized single crystals have a band gap of E-g = 3.32 eV and exhibit anisotropic absorption in the band-edge region near 350 nm, whereas polycrystalline samples are fully transparent in the same frequency range. Using solid-state density functional theory (DFT), the observed size dependence in the optical anisotropy is correlated with the preferred orientation adopted by pyridyl groups under conditions of slow crystal self-assembly. Our work thus paves the way for the development of optical polarization switches based on metal- organic frameworks.

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