Selective Thermal and Photocatalytic Decomposition of Aqueous Hydrazine to Produce H2 over Ag-Modified TiO2 Nanomaterial

被引:3
|
作者
Althabaiti, Shaeel Ahmed [1 ]
Khan, Zaheer [1 ]
Narasimharao, Katabathini [1 ]
Bawaked, Salem Mohamed [1 ]
Al-Sheheri, Soad Zahir [1 ]
Mokhtar, Mohamed [1 ]
Malik, Maqsood Ahmad [2 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Chem Dept, POB 80203, Jeddah 21589, Saudi Arabia
[2] Jamia Millia Islamia, Fac Nat Sci, Dept Chem, New Delhi 110025, India
关键词
H-2; production; Ag-modified TiO2; photocatalysis; hydrazine decomposition; ENHANCED RAMAN-SCATTERING; HYDROGEN GENERATION; DOPED TIO2; TITANIUM-DIOXIDE; ROOM-TEMPERATURE; CHARGE-TRANSFER; CARBON; SILVER; WATER; NANOCOMPOSITES;
D O I
10.3390/nano13142076
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An Ag-modified TiO2 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 TiO2 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 TiO2. In addition, the Raman peak intensity and absorbance were increased after Ag modification onto TiO2. 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 TiO2 nanomaterials was higher than that of bare TiO2 and Ag metal NPs due to the synergistic effect between the Ag metal and TiO2 structures. In addition, the surface plasmon resonance (SPR) electron transfer from Ag metal particles to the conduction band of TiO2 is responsible for superior activity of TiO2-Ag catalyst. The Ag-modified TiO2 nanomaterials offered a 100% H-2 selectivity within 30 min of reaction time and an apparent rate constant of 0.018 min(-1) with an activation energy of 34.4 kJ/mol under visible light radiation.
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页数:21
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