scholarly journals Preparation and Characterization of Copper, Iron, and Nickel Doped Titanium Dioxide Photocatalysts for Decolorization of Methylene Blue

2021 ◽  
Vol 50 (1) ◽  
pp. 135-149
Author(s):  
Jawed Qaderi ◽  
Che Rozid Mamat ◽  
Aishah Abdul Jalil
Keyword(s):  
Titanium Dioxide ◽  
Visible Light ◽  
Uv Light ◽  
Irradiation Time ◽  
Sol Gel ◽  
Light Response ◽  
Pure Tio2 ◽  
Necessary Condition ◽  
Doped Tio2 ◽  
Bet Analysis

The visible-light response is a necessary condition for titanium dioxide (TiO2) photocatalyst to function as a visible light active photocatalyst. This condition can be solved by investigation of the bandgaps and the optimization of doping levels of multivalency metal-doped TiO2. In this study, pure and Cu, Fe, and Ni-doped TiO2 photocatalysts were prepared by the sol‐gel method. The photocatalysts were characterized using XRD, FTIR, FESEM, EDX, N2 physisorption, and UV‐Vis spectrophotometry techniques. The XRD patterns of all pure TiO2 and Cu/TiO2, Fe/TiO2, and Ni/TiO2samples showed the dominant structure of the anatase TiO2 phase. The presence of functional groups at the interface of TiO2 particles was showed by FTIR. The FESEM analysis showed that the particle size of the prepared samples was uniform with spherical morphology. EDX results showed that TiO2 has successfully incorporated Cu, Fe, and Ni metals onto its surface. The BET analysis showed that the specific surface area of the doped samples increased with the amount of doping. The optical properties of all samples were carried out using UV-DRS measurements and their obtained bandgap energies were in the range of 3.22 - 3.42 eV. The pure TiO2 displayed more than 98% and 97% decolorization rates for MB solution at the end of irradiation time of 5 h under UV and visible light, respectively. Among the doped samples, 3 mol% Ni/TiO2 and Cu/TiO2 demonstrated the highest photocatalytic activity (97.65%) under UV light and 6 mol% Ni/TiO2 under visible light for MB (96.86%) decolorization.

scholarly journals Green Synthesis of N/Zr Co-Doped TiO2 for Photocatalytic Degradation of p-Nitrophenol in Wastewater

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 235
Author(s):  
Hayette Benkhennouche-Bouchene ◽  
Julien G. Mahy ◽  
Cédric Wolfs ◽  
Bénédicte Vertruyen ◽  
Dirk Poelman ◽  
...  
Keyword(s):  
Visible Light ◽  
Tio2 Nanoparticles ◽  
Sol Gel ◽  
Visible Region ◽  
Chemical Properties ◽  
Pure Tio2 ◽  
Molar Ratio ◽  
Xps Spectra ◽  
Doped Tio2 ◽  
Co Doped

TiO2 prepared by a green aqueous sol–gel peptization process is co-doped with nitrogen and zirconium to improve and extend its photoactivity to the visible region. Two nitrogen precursors are used: urea and triethylamine; zirconium (IV) tert-butoxide is added as a source of zirconia. The N/Ti molar ratio is fixed regardless of the chosen nitrogen precursor while the quantity of zirconia is set to 0.7, 1.4, 2, or 2.8 mol%. The performance and physico-chemical properties of these materials are compared with the commercial Evonik P25 photocatalyst. For all doped and co-doped samples, TiO2 nanoparticles of 4 to 8 nm of size are formed of anatase-brookite phases, with a specific surface area between 125 and 280 m2 g−1 vs. 50 m2 g−1 for the commercial P25 photocatalyst. X-ray photoelectron (XPS) measurements show that nitrogen is incorporated into the TiO2 materials through Ti-O-N bonds allowing light absorption in the visible region. The XPS spectra of the Zr-(co)doped powders show the presence of TiO2-ZrO2 mixed oxide materials. Under visible light, the best co-doped sample gives a degradation of p-nitrophenol (PNP) equal to 70% instead of 25% with pure TiO2 and 10% with P25 under the same conditions. Similarly, the photocatalytic activity improved under UV/visible reaching 95% with the best sample compared to 50% with pure TiO2. This study suggests that N/Zr co-doped TiO2 nanoparticles can be produced in a safe and energy-efficient way while being markedly more active than state-of-the-art photocatalytic materials under visible light.

scholarly journals Efficient Dye Contaminant Elimination and Simultaneously Electricity Production via a Bi-Doped TiO2 Photocatalytic Fuel Cell

Nanomaterials ◽  
2022 ◽  
Vol 12 (2) ◽  
pp. 210
Author(s):  
Dong Liu ◽  
Chunling Li ◽  
Congyue Zhao ◽  
Er Nie ◽  
Jianqiao Wang ◽  
...  
Keyword(s):  
Fuel Cell ◽  
Visible Light ◽  
Sol Gel ◽  
Oxygen Demand ◽  
Light Response ◽  
Electricity Production ◽  
Doped Tio2 ◽  
Screen Printing Technique ◽  
One Step ◽  
Photocatalytic Fuel Cell

TiO2 develops a higher efficiency when doping Bi into it by increasing the visible light absorption and inhibiting the recombination of photogenerated charges. Herein, a highly efficient Bi doped TiO2 photoanode was fabricated via a one-step modified sol-gel method and a screen-printing technique for the anode of photocatalytic fuel cell (PFC). A maximum degradation rate of 91.2% of Rhodamine B (RhB) and of 89% after being repeated 5 times with only 2% lost reflected an enhanced PFC performance and demonstrated an excellent stability under visible-light irradiation. The excellent degradation performance was attributed to the enhanced visible-light response and decreased electron-hole recombination rate. Meanwhile, an excellent linear correlation was observed between the efficient photocurrent of PFC and the chemical oxygen demand of solution when RhB is sufficient.

Preparation, Characterization, and Photocatalytic Property of N-La Co-Doped TiO2 with Visible Light Response

2012 ◽  
Vol 529 ◽  
pp. 537-540 ◽  
Author(s):  
Gui Hua Li ◽  
An Feng Wang
Keyword(s):  
Visible Light ◽  
Reaction Temperature ◽  
Catalyst Activity ◽  
Sol Gel ◽  
Photocatalytic Property ◽  
Light Response ◽  
Catalyst Amount ◽  
Doped Tio2 ◽  
Sol Gel Process ◽  
Co Doped

N-La co-doped TiO2 has been synthesized via sol-gel process. The XRD result showed that the structure of N-La co-doped TiO2 was anatase. Their performance of photocatalytic degradation of methylene blue under visible light were investigated. The combined effects of catalyst compsition, calcination temperature, catalyst amount and reaction temperature on catalyst activity were investigated. Experiment results depicted that activeness of catalyst N2.5La0.5/TiO2 calcinated at 500°C for 2h was highest. Using this catalyst, when the catalyst amount was 0.35 g/L, the reaction temperature was 40°C the degradation rate of mehylene blue in 4h could reach 96.5%.

scholarly journals Novel hybrid Sr-doped TiO2/magnetic Ni0.6Zn0.4Fe2O4 for enhanced separation and photodegradation of organics under visible light

RSC Advances ◽  
2015 ◽  
Vol 5 (31) ◽  
pp. 24056-24063 ◽  
Author(s):  
Fuming Liu ◽  
Yu Xie ◽  
Changlin Yu ◽  
Xiaoming Liu ◽  
Yuhua Dai ◽  
...  
Keyword(s):  
Titanium Dioxide ◽  
Visible Light ◽  
Organic Pollutants ◽  
Light Response ◽  
Doped Tio2 ◽  
Visible Light Response ◽  
Low Efficiency

Titanium dioxide (TiO2) has been intensively used as a photocatalyst for the degradation of organic pollutants in water, but is typically obstacle by a low efficiency, costly separation, limited visible light response, and poor recyclability.

scholarly journals Synthesis of Porous N-doped TiO2 by Using Peroxo Sol-Gel Method for Photocatalytic Reduction of Cd(II)

2021 ◽  
Vol 17 (1) ◽  
pp. 103-112
Author(s):  
Diana Vanda Wellia ◽  
Dina Nofebriani ◽  
Nurul Pratiwi ◽  
Safni Safni
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Sol Gel ◽  
Photocatalytic Reduction ◽  
Gel Method ◽  
Doped Tio2 ◽  
Sol Gel Method ◽  
Catalytic Active Site ◽  
Bet Analysis

Porous N-doped TiO2 photocatalyst was successfully synthesized by an environmentally friendly peroxo sol-gel method using polyethylene glycol (PEG) as a templating agent. Here, the effect of PEG addition to the aqueous peroxotitanium solutions on the structure, pore properties and photocatalytic activity of the obtained photocatalysts was systematically studied. The prepared photocatalysts were characterized by X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), and Brunauer-Emmett-Teller (BET). It was found that the doping of nitrogen narrows the band gap of TiO2 leading to enhance its visible-light response. The BET analysis shows that the prepared photocatalysts have a typical mesoporous structure with pore sizes of 3–6 nm. The photocatalytic activity of the prepared photocatalysts was evaluated by photocatalytic reduction of Cd(II) in an aqueous solution under visible light irradiation. The results show that porous N-doped TiO2 with the optimal PEG addition had the highest Cd(II) reduction of 85.1% after 2.5 h irradiation in neutral aqueous solution. This significant improvement in photocatalytic activity of the prepared photocatalysts was mainly attributed to the synergistic combination of N doping and porous structure, which could actively increase the catalytic active site of this photocatalysts. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 

scholarly journals Synthesis of Fe- and Co-Doped TiO2 with Improved Photocatalytic Activity Under Visible Irradiation Toward Carbamazepine Degradation

Materials ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 3874 ◽  
Author(s):  
Abderrahim El Mragui ◽  
Yuliya Logvina ◽  
Luís Pinto da Silva ◽  
Omar Zegaoui ◽  
Joaquim C.G. Esteves da Silva
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Diffuse Reflectance Spectroscopy ◽  
Anatase Phase ◽  
Aqueous Suspension ◽  
Sol Gel ◽  
Pure Tio2 ◽  
Doped Tio2 ◽  
Doped Titania ◽  
Co Doped

Pure TiO2 and Fe- and Co-doped TiO2 nanoparticles (NPs) as photocatalysts were synthesized using wet chemical methods (sol-gel + precipitation). Their crystalline structure and optical properties were analyzed using X-ray diffraction (XRD), Raman spectroscopy and Fourier-transform infrared (FTIR) spectroscopy, ultraviolet-visible light (UV-Vis) diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of the synthesized nanoparticles was evaluated through degradation of carbamazepine (CBZ) under UV-A and visible-light irradiations. The XRD and Raman analyses revealed that all synthesized nanomaterials showed only the anatase phase. The DRS results showed that the absorption edge was blue-shifted for Fe-doped TiO2 NPs. The decrease in charge recombination was evidenced from the PL investigation for both Co-doped and Fe-doped TiO2 nanomaterials. An enhancement in photocatalytic degradation of carbamazepine in aqueous suspension under both UV-A light and visible-light irradiations was observed for Fe-doped Titania NPs by comparison with pure TiO2. These results suggest that the doping cations could suppress the electron/hole recombination. Therefore, the photocatalytic activity of TiO2-based nanomaterials was enhanced.

scholarly journals SYNTHESIS, CHARACTERIZATION AND PHOTOACTIVITY EVALUATION OF NITROGEN DOPED TITANIUM DIOXIDE ON METHYLENE BLUE DYE DEGRADATION

2020 ◽  
Vol 4 (3) ◽  
pp. 148-153
Author(s):  
Moses Titus Yilleng ◽  
Moses Sunday ◽  
Doctor Stephen
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Titanium Dioxide ◽  
Diffuse Reflectance Spectroscopy ◽  
Dye Degradation ◽  
Uv Light ◽  
Sol Gel ◽  
Pure Tio2 ◽  
Blue Dye ◽  
Photodegradation Efficiency

Titanium dioxide has proven to be one of the most promising heterogeneous catalyst. This work explores the photocatalytic activity of modified titanium dioxide. Nitrogen was incorporated into mesoporous TiO2 using Sol-gel method. The N-TiO2 was characterized using X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM), Scanning electron microscopy (SEM) thermogravimetric analysis (TGA), and U-Vis diffuse reflectance spectroscopy (DRS). 1%wtN-TiO2 expresses the highest photoactivity in UV light compared to 3%wtN-TiO2 and 5%wt N-TiO2 respectively. The photodegradation efficiency of the catalyst follows the following trend 1%wtN-TiO2 >3%wtN-TiO2 >5%wtN-TiO2>PURE-TiO2. The results obtained from the kinetics investigation shows the following trends 1%wtN-TiO2 is 0.049 s-1, 3%wtN-TiO2 is 0.0289 s-1, 5%wtN-TiO2 is 0.0143 s-1, and the PURE-TiO2 is 0.0118 s-1. The consistency in the rate constant values of the phodegradation of methylene blue; it clearly showed that the reaction follows a pseudo-first order kinetics.

Preparation and Photocatalytic Properties of Nanosized La3+ and Co2+ Co-Doped TiO2 by Microemulsions

2007 ◽  
Vol 336-338 ◽  
pp. 1943-1945
Author(s):  
Wei Liang Liu ◽  
Dan Li Lu ◽  
Chang Chun Ge ◽  
Jian Hua Chen ◽  
Zhi Ping He
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Visible Light ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Uv Light ◽  
Pure Tio2 ◽  
Doped Tio2 ◽  
Co Doped

La3+ and Co2+ co-doped titania nanoparticles were prepared from reacting TiOSO4, La(NO3)3 and Co(NO3)2 with NH4OH in water/Triton X-100/n-hexanol/cyclohexane microemulsions. The structure, surface morphology and the specific surface area of the samples were characterized. The photocatalytic efficiency of as-prepared TiO2 was tested by photodegrading methyl orange. The results showed that doping with La3+ and Co2+ could suppress the growth of TiO2 grains and increase the specific surface area; When the calcination temperature increased from 300°C to 900°C, the average crystallite size of the particles increased from 7.3nm to 35.6 nm andthe specific surface area of the particles decreased rapidly from 205.5m2/g to 41.2m2/g. The synthesized amorphous particles wer transformed into anatase phase at 300°C, and further into rutile phase at 900°C. UV-Vis diffuse reflectance spectrum revealed that La3+ and Co2+ co-doped TiO2 absorbed UV light and visible light, while pure TiO2 could only absorb UV light. In the experiments of photodegrading methyl orange, it was proved that La3+ and Co2+ co-doped TiO2 had high photocatalytic activity under UV light and visible light, while pure TiO2 showed photocatalytic activity just under UV light.

scholarly journals Reforming Characteristics under Visible Light Response of Cr- or Ag-Doped Prepared by Sol-Gel and Dip-Coating Process

2012 ◽  
Vol 2012 ◽  
pp. 1-12 ◽  
Author(s):  
Akira Nishimura ◽  
Go Mitsui ◽  
Katsuya Nakamura ◽  
Masafumi Hirota ◽  
Eric Hu
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Sol Gel ◽  
Light Response ◽  
Dip Coating ◽  
Coating Process ◽  
Ag Doping ◽  
Visible Light Response ◽  
Cr Doping ◽  
Doping Case

A Cr- or Ag-doped TiO2film was prepared by sol-gel and dip-coating process and used as the photocatalyst for CO2reforming under the visible light. The ratio of amount of Cr or Ag added to amount of Ti in TiO2sol solution (R) varied from 0 to 100 wt% or 0 to 50 wt%, respectively. The total layer number of Cr- or Ag-doped TiO2film (N) coated was changed. The CO2reforming performance with the Cr- or Ag-doped TiO2film was tested under a Xe lamp with or without ultraviolet (UV) light. As a result, whenNequals to 1, the concentration of CO which was a product from CO2reforming was maximized in Cr doping case forR= 70 wt% and in Ag doping case forR= 1 wt%, respectively. The best result of concentration of CO = 8306 ppmV, concentration of CH4= 1367 ppmV, concentration of C2H6= 1712 ppmV is obtained when with Cr doping in this study.

Photocatalytic Activity of Bismuth Ferrite Nanoparticles Synthesized via Sol-Gel Route

2019 ◽  
Vol 233 (5) ◽  
pp. 595-607 ◽  
Author(s):  
Mohsin Siddique ◽  
Noor Muhammad Khan ◽  
Muhammad Saeed
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Irradiation Time ◽  
Bismuth Ferrite ◽  
Sol Gel ◽  
Reaction System ◽  
Light Conditions ◽  
X Ray Diffraction ◽  
Light Region ◽  
Gel Technique

Abstract Nanosized, magnetically separable bismuth ferrite (BFO) nanoparticles, pertaining a crystallite size in the range of 14–15 nm were prepared via facile sol-gel technique. The product was characterized by scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. The product was explored for the photocatalytic mineralization of rhodamine B (RB) dye in aqueous medium. The effect of different investigational parameters such as amount of photocatalyst, initial dye concentration and irradiation time on the photocatalytic degradation of RB was studied. The results reveal that the catalyst shows good degrading ability under normal pH and visible light conditions. BFO nanoparticles demonstrated a strong absorption ability in the visible-light region, which lead to efficient photocatalytic degradation of RB dye The reaction system was heterogeneous in nature in which the catalyst can be separated by a normal magnet.

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