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Effective Photocatalytic Activity of Mixed Ni/Fe-Base Metal-Organic Framework under a Compact Fluorescent Daylight Lamp
- Source :
- Catalysts, Vol 8, Iss 11, p 487 (2018)
- Publication Year :
- 2018
- Publisher :
- MDPI AG, 2018.
-
Abstract
- Mixed Ni/Fe-base metal-organic framework (Ni/Fe-MOF) with different molar ratios of Ni2+/Fe3+ have been successfully produced using an appropriate solvothermal router. Physicochemical properties of all samples were characterized using X-ray diffraction (XRD), Raman, field emission scanning electron microscopes (FE-SEM), fourier-transform infrared spectroscopy (FT-IR), N2 adsorption-desorption analysis, X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectra (UV-Vis DRS), and photoluminescence spectra (PL). The photocatalytic degradation performances of the photocatalysts were evaluated in the decomposition of rhodamine B (RhB) under a compact fluorescent daylight lamp. From XRD, IR, XPS, and Raman results, with the presence of mixed ion Fe3+ and Ni2+, MIL-88B (MIL standing for Materials of Institut Lavoisier) crystals based on the mixed metal Fe2NiO cluster were formed, while MIL-53(Fe) was formed with the presence of single ion Fe3+. From UV-Vis DRS results, Ni/Fe-MOF samples exhibited the absorption spectrum up to the visible region, and then they showed the high photocatalytic activity under visible light irradiation. A Ni/Fe-MOF sample with a Ni2+/Fe3+ molar ratio of 0.3 showed the highest photocatalytic degradation capacity of RhB, superior to that of the MIL-53(Fe) sample. The obtained result could be explained as a consequence of the large surface area with large pore volumes and pore size by the Ni2+ incorporating into the MOF’s structure. In addition, a mixed metal Fe/Ni-based framework consisted of mixed-metal cluster Fe2NiO with an electron transfer effect and may enhance the photocatalytic performance.
Details
- Language :
- English
- ISSN :
- 20734344
- Volume :
- 8
- Issue :
- 11
- Database :
- Directory of Open Access Journals
- Journal :
- Catalysts
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.2fd0642a7be1417ba437e28cfe6827b4
- Document Type :
- article
- Full Text :
- https://doi.org/10.3390/catal8110487