Selective Thermal and Photocatalytic Decomposition of Aqueous Hydrazine to Produce H[sub.2] over Ag-Modified TiO[sub.2] Nanomaterial
An Ag-modified TiO[sub.2] nanomaterial was prepared by a one-pot synthesis method using tetra butyl titanate, silver nitrate, and sodium hydroxide in water at 473 K for 3 h. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy were used to determine the structure and...
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Veröffentlicht in: | Nanomaterials (Basel, Switzerland) Switzerland), 2023-07, Vol.13 (14) |
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Sprache: | eng |
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Zusammenfassung: | An Ag-modified TiO[sub.2] nanomaterial was prepared by a one-pot synthesis method using tetra butyl titanate, silver nitrate, and sodium hydroxide in water at 473 K for 3 h. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy were used to determine the structure and morphology of the synthesized Ag-modified TiO[sub.2] nanomaterial. The diffuse reflectance UV-visible and photoluminescence spectroscopy results revealed that metallic Ag nanoparticles decreased the optical band gap and photoluminescence intensity of the TiO[sub.2]. In addition, the Raman peak intensity and absorbance were increased after Ag modification onto TiO[sub.2]. The photocatalytic efficiency of the synthesized samples was tested for decomposition of aqueous hydrazine solution under visible light irradiation. The photocatalytic efficiency of Ag-modified TiO[sub.2] nanomaterials was higher than that of bare TiO[sub.2] and Ag metal NPs due to the synergistic effect between the Ag metal and TiO[sub.2] structures. In addition, the surface plasmon resonance (SPR) electron transfer from Ag metal particles to the conduction band of TiO[sub.2] is responsible for superior activity of TiO[sub.2]-Ag catalyst. The Ag-modified TiO[sub.2] nanomaterials offered a 100% H[sub.2] selectivity within 30 min of reaction time and an apparent rate constant of 0.018 min[sup.−1] with an activation energy of 34.4 kJ/mol under visible light radiation. |
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ISSN: | 2079-4991 2079-4991 |
DOI: | 10.3390/nano13142076 |