scholarly journals Influencing Factors in the Synthesis of Photoactive Nanocomposites of ZnO/SiO2-Porous Heterostructures from Montmorillonite and the Study for Methyl Violet Photodegradation

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3427
Author(s):  
Is Fatimah ◽  
Gani Purwiandono ◽  
Putwi Widya Citradewi ◽  
Suresh Sagadevan ◽  
Won-Chun Oh ◽  
...  

In this work, photoactive nanocomposites of ZnO/SiO2 porous heterostructures (PCHs) were prepared from montmorillonite clay. The effects of preparation methods and Zn content on the physicochemical features and photocatalytic properties were investigated. Briefly, a comparison of the use of hydrothermal and microwave-assisted methods was done. The Zn content was varied between 5 and 15 wt% and the characteristics of the nanomaterials were also examined. The physical and chemical properties of the materials were characterized using X-ray diffraction, diffuse-reflectance UV-Vis, X-ray photoelectron spectroscopy, and gas sorption analyses. The morphology of the synthesized materials was characterized through scanning electron microscopy and transmission electron microscopy. The photocatalytic performance of the prepared materials was quantified through the photocatalytic degradation of methyl violet (MV) under irradiation with UV and visible light. It was found that PCHs exhibit greatly improved physicochemical characteristics as photocatalysts, resulting in boosting photocatalytic activity for the degradation of MV. It was found that varied synthesis methods and Zn content strongly affected the specific surface area, pore distribution, and band gap energy of PCHs. In addition, the band gap energy was found to govern the photoactivity. Additionally, the surface parameters of the PCHs were found to contribute to the degradation mechanism. It was found that the prepared PCHs demonstrated excellent photocatalytic activity and reusability, as seen in the high degradation efficiency attained at high concentrations. No significant changes in activity were seen until five cycles of photodegradation were done.

2013 ◽  
Vol 772 ◽  
pp. 365-370 ◽  
Author(s):  
Mohd Hasmizam Razali ◽  
M.N. Ahmad-Fauzi ◽  
Abdul Rahman Mohamed ◽  
Srimala Sreekantan

Titanium dioxide (TiO2) nanoparticles were successfully synthesised by hydrothermal method using TiO2 microparticle powder (Merck) as precursor. TiO2 microparticles powder (~160 nm) was mixed with 10 M NaOH and treated hydrothermally at 150 °C and 2 MPa pressure in autoclave for 24 hours. After hydrothermal reaction was completed, the sample was washed, dried and heated at 500 °C for 2 hours to produce TiO2 nanoparticles. The synthesised nanoparticles were characterized using field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and raman spectroscopy. UV-Vis DRS was used to determine the band gap energy. Field emissions and transmissions electron microscopy images revealed that nanoparticles obtained was about 14 nm. X-ray diffraction patterns showed that TiO2 nanoparticles were anatase phase (tetragonal). The band gap energy of TiO2 nanoparticles was determined to be 3.32 eV.


2014 ◽  
Vol 781 ◽  
pp. 63-78 ◽  
Author(s):  
S. Prabhu ◽  
A. Nithya ◽  
S. Chandra Mohan ◽  
Kandasamy Jothivenkatachalam

Titania has been studied to be one of the best photocatalysts for the decomposition of many organic pollutants present in aqueous medium. Because of the wide band gap energy of TiO2 (3.2 eV) it can be activated only under UV light region which is present 4 % in the solar light spectrum. The photocatalytic activity of TiO2 was enhanced by means of several methods. TiO2 coupled with other semiconductor has gained additional importance, owing to improving the efficient charge separation by trapping the photogenerated electrons. WO3 is a better semiconductor having relatively lower band gap energy (2.8 eV) and absorb broad solar light spectrum. The formation of WOx monolayer on TiO2 notably increases the surface acidity of TiO2. This increasing the surface acidity of WO3/TiO2 photocatalyst facilitates the adsorption of the more hydroxyl group in addition to more organic reactants on its surface which obviously facilitate the enhancement of photocatalytic activity. In this review, the synthesis methods and photocatalytic activity of some selected and unique results related to WO3/TiO2 photocatalyst were discussed. The efficient charge separation, increased absorption of the reactants by increasing the surface acidity and high aspect ratio structures of WO3/TiO2 are also reviewed.


2020 ◽  
Vol 20 (6) ◽  
pp. 1392
Author(s):  
Leny Yuliati ◽  
Mohd Hayrie Mohd Hatta ◽  
Siew Ling Lee ◽  
Hendrik Oktendy Lintang

In this work, the crystalline carbon nitride photocatalysts were synthesized by an ionothermal technique with varied synthesis temperature of 500, 550, and 600 °C, and synthesis time of 2, 4, and 6 h. Fourier transform infrared spectra showed the successful formation of the prepared carbon nitrides from their characteristic vibration peaks. X-ray diffraction patterns suggested that the same phase of poly(triazine imide) and heptazine could be observed, but with different crystallinity. The optical properties showed that different temperatures and synthesis time resulted in the different band gap energy (2.72–3.02 eV) as well as the specific surface area (24–73 m2 g–1). The transmission electron microscopy image revealed that the crystalline carbon nitride has a near-hexagonal prismatic crystallite size of about 50 nm. Analysis by high-performance liquid chromatography showed that the best photocatalytic activity for phenol degradation under solar light simulator was obtained on the crystalline carbon nitride prepared at the 550 °C for 4 h, which would be due to the high crystallinity, suitable low band gap energy (2.82 eV), and large specific surface area (73 m2 g–1). Controlling both the temperature and synthesis time is shown to be important to obtain the best physicochemical properties leading to high activity.


2017 ◽  
Vol 889 ◽  
pp. 234-238
Author(s):  
Mohd Hasmizam Razali ◽  
Nur Arifah Ismail ◽  
Mahani Yusoff

Pure and F doped TiO2 nanotubes was synthesized using simple hydrothermal method. The hydrothermal was conducted using teflon-liner autoclave and maintained at 150oC for 24 hours. The characterization of synthesised product was carried out using x-ray diffraction (XRD), transmission electron microscope (TEM), energy dispersive of x-ray spectroscopy (EDX) and ultra violet – visible light diffuse reflectance spectroscopy (UV-Vis DRS) for band gap measurements. XRD patterns indicated that anatase TiO2 phase was remained after F doping suggested that fluorine was highly dispersed into TiO2 by substituted with O in the TiO2 lattice to formed TiO2-xFx solid solution. Morphology investigation using TEM found out small diameter of nanotubes structure within 8 – 10 nm of pure and F doped TiO2 nanotubes. The band gap energy (Eg) of both nanotubes samples were almost similar proposing that F doping does not modify the band gap energy.


Crystals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 968
Author(s):  
Reina Galeazzi Isasmendi ◽  
Isidro Juvenal Gonzalez Panzo ◽  
Crisóforo Morales-Ruiz ◽  
Román Romano Trujillo ◽  
Enrique Rosendo ◽  
...  

Copper oxide (CuO) films were deposited onto glass substrates by the microwave assisted chemical bath deposition method, and varying the pH of the solution. The pH range was varied from 11.0 to 13.5, and the effects on the film properties were studied. An analytical study of the precursor solution was proposed to describe and understand the chemical reaction mechanisms that take place in the chemical bath at certain pH to produce the CuO film. A series of experiments were performed by varying the parameters of the analytical model from which the CuO films were obtained. The crystalline structure of the CuO films was studied using X-ray diffraction, while the surface morphology, chemical composition, and optical band-gap energy were analyzed by scanning electron microscopy, X-ray photoelectron spectroscopy, and UV–Vis spectrophotometry, respectively. The CuO films obtained exhibited a monoclinic crystalline phase, nanostructured surface morphology, stoichiometric Cu/O ratio of 50/50 at%, and band-gap energy value of 1.2 eV.


Author(s):  
Anuar Kassim ◽  
Tan Wee Tee ◽  
Ho Soon Min ◽  
Shanthi Monohorn ◽  
Saravanan Nagalingam

PbSe thin films are prepared by chemical bath deposition technique over microscope glass substrates from an aqueous acidic bath containing lead nitrate and sodium selenate. The influence of bath temperature on the properties of PbSe film is investigated. The X-ray diffraction analysis showed the deposited films were polycrystalline and having the (111) orientation. The surface morphology study revealed that the grains have cubic shape crystal. The band gap energy was decreased from 2.0 to 1.3 eV as the bath temperature was increased from 40 to 80°C. The films deposited at 80°C showed good crystallinity and uniformly distributed over the surface of substrate with larger grain sizes. Therefore, the optimum bath temperature is 80°C. Keywords: Lead selenide; X-ray diffraction; Band gap energy; Chemical bath deposition; Thin films DOI: 10.3126/kuset.v6i2.4021Kathmandu University Journal of Science, Engineering and Technology Vol.6. No II, November, 2010, pp.126-132


2014 ◽  
Vol 925 ◽  
pp. 200-204
Author(s):  
Leny Yuliati ◽  
Melody Kimi ◽  
Mustaffa Shamsuddin

Zinc sulfide (ZnS) has been reported to act as a photocatalyts to reduce water to hydrogen. However, ZnS could not work under visible light irradiation due to its large band gap energy. In order to improve the performance of ZnS, Ga and Sn were doped to ZnS. The series of Ga (0.1),Sn (x)-ZnS with various amounts of Sn (x) was prepared by hydrothermal method. XRD patterns suggested that the addition of Ga might reduce the crystallinity of ZnS, suggesting that Ga might inhibit the crystal growth or agglomeration of ZnS. On the other hand addition of Sn did not much affect the structure of the Ga (0.1)-ZnS. The DR UU-visible spectra confirmed the red shift of the absorption edge with the addition of Ga due to the reduced band gap energy, while the addition of Sn did not much shift the absorption edge of the Ga (0.1)-ZnS to longer wavelength. FESEM images showed that all the prepared samples have sphere-shaped particles and no remarkable change was observed with the addition of Ga or Sn. The photocatalytic hydrogen production from water was carried out at room temperature in the presence of sacrificial agent under visible light irradiation. While ZnS did not show activity under visible light, all the prepared Ga (0.1)-ZnS and Ga (0.1),Sn (x)-ZnS samples exhibited photocatalytic activity for hydrogen production. The highest hydrogen production was achieved on Ga (0.1),Sn (0.01)-ZnS, which activity was ca. three times higher than that of the single doped Ga (0.1)-ZnS. This study clearly showed that Sn acted as a good co-dopant to increase the photocatalytic activity of Ga (0.1)-ZnS for hydrogen production from water under visible light irradiation.


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