Hydrothermal Synthesis and Photocatalytic Properties of TiO2/SnS2 Nanocomposite

2014 ◽  
Vol 898 ◽  
pp. 23-26
Author(s):  
Jing Li ◽  
Wei Sun ◽  
Wei Min Dai ◽  
Yong Cai Zhang

TiO2/SnS2 nanocomposite was synthesized via hydrothermal treatment of tin (IV) chloride pentahydrate, thioacetamide and TiO2 nanotubes in deionized water at 150 °C for 3 h. The structure, composition and optical property of the as-synthesized nanocomposite were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy and UV-vis diffuse reflectance spectra, and its photocatalytic property was tested in the reduction of aqueous Cr6+ under visible-light (λ > 420 nm) irradiation. It was observed that TiO2 nanotubes exhibited no photocatalytic activity, whereas TiO2/SnS2 nanocomposite exhibited photocatalytic activity in the reduction of aqueous Cr6+ under visible-light (λ > 420 nm) irradiation.

NANO ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. 1650114 ◽  
Author(s):  
Dan Li ◽  
Jianwei Li ◽  
Caiqin Han ◽  
Xinsheng Zhao ◽  
Haipeng Chu ◽  
...  

Few-layered MoS2 nanostructures were successfully synthesized by a simple hydrothermal method without the addition of any catalysts or surfactants. Their morphology, structure and photocatalytic activity were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, electrochemical impedance spectra and UV-Vis absorption spectroscopy, respectively. These results show that the MoS2 nanostructures synthesized at 180[Formula: see text]C exhibit an optimal visible light photocatalytic activity (99%) in the degradation of Rhodamine B owing to the relatively easier adsorption of pollutants, higher visible light absorption and lower electron–hole pair recombination.


2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding

Abstract The g-C3N4 nanosheet was prepared by calcination method, the MoS2 nanosheet was prepared by hydrothermal method. The g-C3N4/MoS2 composites were prepared by ultrasonic composite in anhydrous ethanol. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), and photoluminescence (PL) techniques were used to characterize the materials. The photocatalytic degradation of Rhodamine B (Rh B) by g-C3N4/MoS2 composites with different mass ratios was investigated under visible light. The results show that a small amount of MoS2 combined with g-C3N4 can significantly improve photocatalytic activity. The g-C3N4/MoS2 composite with a mass ratio of 1:8 has the highest photocatalytic activity, and the degradation rate of Rh B increases from 50% to 99.6%. The main reason is that MoS2 and g-C3N4 have a matching band structure. The separation rate of photogenerated electron-hole pairs is enhanced. So the g-C3N4/MoS2 composite can improve the photocatalytic activity. The photocatalytic mechanism was proposed through the active matter capture experiment.


Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2303 ◽  
Author(s):  
Yinxia Chen ◽  
Xianbing Ji ◽  
Vadivel Sethumathavan ◽  
Bappi Paul

In this present work, we synthesized a yolk-shell shaped CuCo2S4 by a simple anion exchange method. The morphological and structural properties of the as-synthesized sample were characterized using X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (UV-vis DRS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The SEM and TEM results confirmed that the uniform yolk-shell structure was formed during the solvothermal process. The band gap was about 1.41 eV, which have been confirmed by UV–vis DRS analysis. The photocatalytic property was evaluated by the photocatalytic degradation of methylene blue (MB) dye as a target pollutant under the visible-light irradiation. The experimental results confirmed the potential application of yolk-shell shape CuCo2S4 in visible-light photocatalytic applications.


RSC Advances ◽  
2015 ◽  
Vol 5 (54) ◽  
pp. 43473-43479 ◽  
Author(s):  
Yanli Xu ◽  
Mengmeng Lv ◽  
Hanbiao Yang ◽  
Qi Chen ◽  
Xueting Liu ◽  
...  

The BiVO4/MIL-101 composite and pure materials were characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, UV-vis diffuse reflectance absorption spectra and photoluminescence emission spectra.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Yunling Zou ◽  
Xianshou Huang ◽  
Tao Yu ◽  
Xiaoqiang Tong ◽  
Yan Li ◽  
...  

Abstract Cu-doped TiO2 having a brookite phase and showing enhanced visible light photocatalytic activity was synthesized using a mild solvothermal method. The as-prepared samples were characterized by various techniques, such as X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy. Photocatalytic activity of Cu-doped brookite TiO2 nanoparticles was evaluated by photodegradation of methylene blue under visible light irradiation. The X-ray diffraction analysis showed that the crystallite size of Cu-doped brookite TiO2 samples decreased with the increase of Cu concentration in the samples. The UV-Vis diffuse reflectance spectroscopy analysis of the Cu-doped TiO2 samples showed a shift to lower energy levels in the band gap compared with that of bare phase brookite TiO2. Cu doped brookite TiO2 can obviously improve its visible light photocatalytic activity because of Cu ions acting as electron acceptors and inhibiting electron-hole recombination. The brookite TiO2 sample with 7.0 wt.% Cu showed the highest photocatalytic activity and the corresponding degradation rate of MB (10 mg/L) reached to 87 % after visible light illumination for 120 min, much higher than that of bare brookite TiO2 prepared under the same conditions (78 %).


Author(s):  
Yaping Guo ◽  
Jianyang Sun ◽  
Hui Chang ◽  
Xu Zhao

A simple, effective and environmental-friendly method was adopted for enhancing the photocatalytic activity of g-C3N4 in the reduction of aqueous Cr(Ⅵ) under visible-light irradiation. The enhancement was achieved via treatment of g-C3N4 in organic solvent with addition of NaOH particles by ultrasonic process for two hours. The results demonstrated that the treated g-C3N4 exhibited much higher photocatalytic activity than pristine g-C3N4 in the reduction of Cr(VI) . Under visible light irradiation for 120 min, the reduced ratios of Cr(VI) with the initial concentration of 50 mg/L in the presence of the treated g-C3N4and pristine g-C3N4 were 100% and 37.1%, respectively. With the addition of fulvic acid, Cr(VI) was efficiently removed at 40 min. Based on the characterization results of the structures and other physiochemical properties of the treated g-C3N4 and pristine g-C3N4 by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and UV Vis diffuse reflectance, the possible reasons responsible for the enhanced photocatalytic activity of the treated g-C3N4 were proposed. The yield and mechanism of different exfoliation methods were compared by semi-quantitative method.


Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 899
Author(s):  
Murendeni P. Ravele ◽  
Opeyemi A. Oyewo ◽  
Damian C. Onwudiwe

Pure-phase Cu2−xS (x = 1, 0.2) nanoparticles have been synthesized by the thermal decomposition of copper(II) dithiocarbamate as a single-source precursor in oleylamine as a capping agent. The compositions of the Cu2−xS nanocrystals varied from CuS (covellite) through the mixture of phases (CuS and Cu7.2S4) to Cu9S5 (digenite) by simply varying the temperature of synthesis. The crystallinity and morphology of the copper sulfides were studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), which showed pure phases at low (120 °C) and high (220 °C) temperatures and a mixture of phases at intermediate temperatures (150 and 180 °C). Covellite was of a spherical morphology, while digenite was rod shaped. The optical properties of these nanocrystals were characterized by UV−vis–NIR and photoluminescence spectroscopies. Both samples had very similar absorption spectra but distinguishable fluorescence properties and exhibited a blue shift in their band gap energies compared to bulk Cu2−xS. The pure phases were used as catalysts for the photocatalytic degradation of tetracycline (TC) under visible-light irradiation. The results demonstrated that the photocatalytic activity of the digenite phase exhibited higher catalytic degradation of 98.5% compared to the covellite phase, which showed 88% degradation within the 120 min reaction time using 80 mg of the catalysts. The higher degradation efficiency achieved with the digenite phase was attributed to its higher absorption of the visible light compared to covellite.


2014 ◽  
Vol 809-810 ◽  
pp. 890-894
Author(s):  
Dan Li ◽  
Lian Wei Shan ◽  
Gui Lin Wang ◽  
Li Min Dong ◽  
Wei Li ◽  
...  

Boron-BiVO4 samples were synthesized by sol-gel method. They were characterized by UV-vis diffuse reflectance spectroscopy, X-ray diffraction. Photocatalytic activity of the obtained BiVO4 samples was investigated through degrading methylene blue (MB). The results reveal that boron-BiVO4 catalysts have monoclinic scheelite structure. The BiVO4 and Co-BiVO4 photocatalysts were responsive to visible light. Co-BiVO4 photocatalyst showed higher photocatalytic activity than pure BiVO4, resulting in the significantly improved efficiency of degradation of MB.


2021 ◽  
Vol 1035 ◽  
pp. 1043-1049
Author(s):  
Di Xiang ◽  
Chang Long Shao

A simple route has been developed for the synthesis of Ag2O/ZnO heterostructures and the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS) and photoluminescence (PL) spectroscopy analysis. Considering the porous structure of Ag2O/ZnO, the photocatalytic degradation for the organic dyes, such as eosin red (ER), methyl orange (MO), methylene blue (MB) and rhodamine B (RhB), under visible light irradiation was investigated in detail. Noticeably, Ag2O/ZnO just took 40 min to degrade 96 % MB. The rate of degradation using the Ag2O/ZnO heterostructures was 2.3 times faster than that of the bare porous ZnO nanospheres under visible light irradiation due to that the recombination of the photogenerated charge was inhibited greatly in the p-type Ag2O and n-type ZnO semiconductor. So the Ag2O/ZnO heterostuctures showed the potential application on environmental remediation.


2011 ◽  
Vol 110-116 ◽  
pp. 547-552 ◽  
Author(s):  
Yu Xin Wang ◽  
Jing Xu ◽  
Xing Guo Cheng ◽  
Hong Fang Xu ◽  
Li Jun Liu

ZnO nanostructures with different morphology have been successfully fabricated by a simple relative low temperature approach at 90 °C for 5 h without surfactant assistance. These structures can be easily tailed using varied concentrations of sodium hydroxide (NaOH) and different amounts of the hydrazine hydrate (N2H4·H2O). X-ray diffraction (XRD) result proves the formation of ZnO with wurtzite structure. Microstructure as revealed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) indicates that the rod-like and chrysanthemum-like ZnO nanostructures contain many radial nanorods, which grow along the [0001] direction. Furthermore, the as-prepared ZnO nanomaterials exhibit high activity on the photo-catalytic degradation of typical persistent organic pollutants (POPs), indicating that they are promising as semiconductor photo-catalysts.


Sign in / Sign up

Export Citation Format

Share Document