Abstract

A new metal organic framework {[Co3(BTC)2(Bimb)2.5]·2H2O}n(1) (Bimb = 1,4-bis[(1H-imidazol-1-yl)methyl]benzene and H3BTC = 1,3,5-Benzenetricarboxylic acid) has been synthesized and structurally characterized by elemental analysis, single-crystal X-ray diffraction (SC-XRD), vary temperature powder X-ray diffraction (VT-PXRD) and vary temperature Fourier transform infrared spectroscopy (VT-FTIR) have been used to establish the complex (1) and its physico-chemical analysis.. According to single crystal structure analysis, complex (1) features a three-dimensional network made up of trinuclear cobalt constructed by two-dimensional layer supported by BTC3− and Bimb ligands. Variable temperature luminescence relationship of as-prepared and excited form of complex (1) investigated luminescence emission in the region of 441-461 nm (2.81-2.69 eV) at room temperature with little difference in physical facade. Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDAX), VT-PXRD and VT-FTIR studies revealed globular shaped Co3O4 nanoparticles with average sizes of about 20 nm as a result of thermal breakdown of (1). The photocatalytic experiments revealed that complex (1) displayed efficient photocatalytic capabilities to decompose the Fluorescein, Eriochrome Black T, Methyl Violet, Crystal Violet, Methyl Orange, Rhodamine B, Methylene Blue, Rhodamine 6G, Neutral Red and Congo Red under UV light irradiation. The photodegradation of FS, EBT, MV, CV, MO, RhB, MB, Rh6G, NR and CR exposed to be 91.7, 77.5, 68.7, 53.9, 50.9, 50.8, 47.4, 38.1, 19.5 and 15.8 %, respectively, after 135 minutes of irradiation with as-prepared MOF (1).

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