scholarly journals Composite Magnetic Photocatalyst Bi5O7I/MnxZn1−xFe2O4: Hydrothermal-Roasting Preparation and Excellent Photocatalytic Activity

Nanomaterials ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 118 ◽  
Author(s):  
Hailong Wang ◽  
Longjun Xu ◽  
Chenglun Liu ◽  
Yuan Lu ◽  
Qi Feng ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Energy Gap ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
Magnetic Photocatalyst ◽  
Transmission Electron ◽  
Excellent Photocatalytic Activity ◽  
Average Recovery Rate

A new composite magnetic photocatalyst, Bi5O7I/MnxZn1−xFe2O4, prepared by a hydrothermal-roasting method was studied. The photocatalytic properties of Bi5O7I/MnxZn1−xFe2O4 were evaluated by degradation of Rhodamine B (RhB) under simulated sunlight irradiation, and the structures and properties were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet-visible light (UV-Vis) diffuse reflectance spectra (DRS), and a vibrating sample magnetometer (VSM). The results indicated that Bi5O7I/MnxZn1−xFe2O4 was an orthorhombic crystal, which was similar to that observed for Bi5O7I. Bi5O7I/MnxZn1−xFe2O4 consisted of irregularly shaped nanosheets that were 40–60 nm thick. The most probable pore size was 24.1 nm and the specific surface area was 7.07 m2/g. Bi5O7I/MnxZn1−xFe2O4 could absorb both ultraviolet and visible light, and the energy gap value was 3.22 eV. The saturation magnetization, coercivity and residual magnetization of Bi5O7I/MnxZn1−xFe2O4 were 3.9 emu/g, 126.6 Oe, and 0.7 emu/g respectively, which could help Bi5O7I/MnxZn1−xFe2O4 be separated and recycled from wastewater under the action of an external magnetic field. The recycling experiments revealed that the average recovery rate of the photocatalyst was 90.1%, and the photocatalytic activity was still more than 81.1% after five cycles.

Few-Layered MoS2 Nanostructures for Highly Efficient Visible Light Photocatalysis

NANO ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. 1650114 ◽  
Author(s):  
Dan Li ◽  
Jianwei Li ◽  
Caiqin Han ◽  
Xinsheng Zhao ◽  
Haipeng Chu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Electrochemical Impedance ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
Electrochemical Impedance Spectra ◽  
X Ray ◽  
Transmission Electron ◽  
Electron Hole Pair

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.

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
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Diffuse Reflectance ◽  
Photocatalytic Property ◽  
Deionized Water ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Chloride Pentahydrate

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.

scholarly journals Preparation of g-C3N4/MoS2 Composite Material and Its Visible Light Catalytic Performance

2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Photogenerated Electron ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Calcination Method

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.

Novel p–n junction UiO-66/BiOI photocatalysts with efficient visible-light-induced photocatalytic activity

2018 ◽  
Vol 77 (5) ◽  
pp. 1441-1448 ◽  
Author(s):  
Yuejin Li ◽  
Xili Shang ◽  
Changhai Li ◽  
Xiaoming Huang ◽  
Jingjing Zheng
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Salicylic Acid ◽  
Visible Light ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Uv Visible ◽  
Adsorption Desorption ◽  
Junction Structure ◽  
First Time

Abstract Novel visible-light-induced UiO-66/BiOI photocatalysts with a p–n junction structure have been prepared for the first time through a facile hydrothermal method. The prepared photocatalysts were characterized using the powder X-ray diffraction, high resolution transmission electron microscopy, scanning electron microscopy, UV–visible diffuse reflectance spectra, and N2 adsorption–desorption (Brunauer–Emmett–Teller) techniques respectively. The photodegradation performances of UiO-66/BiOI photocatalysts were evaluated by photodegrading salicylic acid under visible-light irradiation. The UiO-66/BiOI composites displayed much higher photocatalytic efficiencies than pure BiOI under visible light. When the content of UiO-66 was 5.2 wt%, the composite (UiO-66/BiOI-2) has the best photocatalytic activity. Most of the salicylic acid molecules can be degraded in 100 min. The degradation rate of UiO-66/BiOI-2 samples is higher than single BiOI and UiO-66. The enhanced photocatalytic performance of UiO-66/BiOI may be ascribed to the formation of p–n heterojunctions between BiOI and UiO-66, which facilitates the transfer and separation of the photogenerated charge carriers. After recycling of the photocatalyst for five times for the photodegradation of salicylic acid, more than 85% of salicylic acid could still be degraded in the fifth cycle, implying that the as-prepared photocatalysts are highly stable.

Synthesis of LaMnO3–Diamond Composites and Their Photocatalytic Activity in the Degradation of Weak Acid Red C-3GN

NANO ◽  
2018 ◽  
Vol 13 (10) ◽  
pp. 1850121 ◽  
Author(s):  
Hao Huang ◽  
Benqian Lu ◽  
Yuanyuan Liu ◽  
Xeuqian Wang ◽  
Jie Hu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Active Sites ◽  
Sol Gel ◽  
Peak Position ◽  
Weak Acid ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Excellent Photocatalytic Activity ◽  
The Fourier Transform

In this study, a series of LaMnO3–diamond composites with varied LaMnO3 mass contents supported on micro-diamond have been synthesized using a sol–gel method. The as-prepared composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy and the Fourier transform infrared spectra (FTIR). Meanwhile, the photocatalytic performances were also tested by photoluminescence (PL) spectroscopy, ultraviolet–visible diffuse reflection spectra (UV-Vis DRS) and the degradation of weak acid red C-3GN (RC-3GN). Results show that the peak position of LaMnO3 is shifted to low angle after the introduction of diamond, and perovskite particles uniformly distributed on the surface of diamond, forming a network structure, which can increase the active sites and the absorption of dye molecules. When the mass ratio of LaMnO3 and diamond is 1:2 (LMO–Dia-2), the composite shows the most excellent photocatalytic activity. This result offers a sample route to enlarge the range of the application of micro-diamond and provide a new carrier for perovskite photocatalysts.

scholarly journals Direct Exfoliation of g-C3N4 with Addition of NaOH for Enhanced Photocatalytic Cr(Ⅵ) Reduction

2018 ◽  
Author(s):  
Yaping Guo ◽  
Jianyang Sun ◽  
Hui Chang ◽  
Xu Zhao
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
Physiochemical Properties ◽  
X Ray ◽  
Transmission Electron ◽  
Ultrasonic Process

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.

scholarly journals One-Step Synthesis of MoS2/TiSi2 via an In Situ Photo-Assisted Reduction Method for Enhanced Photocatalytic H2 Evolution under Simulated Sunlight Illumination

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 299 ◽  
Author(s):  
Chunyong Zhang ◽  
Aijuan Liu ◽  
Kezhen Li ◽  
Yukou Du ◽  
Ping Yang
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Response Spectrum ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Complex Catalyst ◽  
Transmission Electron ◽  
One Step

A new MoS2/TiSi2 complex catalyst was designed and synthesized by a simple one-step in situ photo-assisted reduction procedure. The structural and morphological properties of the composites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and ultraviolet-visible diffused reflectance spectroscopy (UV-vis DRS), which proved the formation of MoS2/TiSi2. MoS2/TiSi2 with optimized composition showed obviously enhanced photocatalytic activity and superior durability for water reduction to produce H2. The H2 generation rate over the MoS2/TiSi2 photocatalyst containing 3 wt % MoS2 reached 214.1 μmol·h−1·g−1 under visible light irradiation, which was ca. 5.6 times that of the pristine TiSi2. The improved photocatalytic activity of MoS2/TiSi2 could be related to the broad response spectrum, large visible light absorption, and synergies among MoS2 and TiSi2 that enhance photoexcited charge transfer and separation.

HYDROTHERMAL SYNTHESIS AND ENHANCED VISIBLE-LIGHT PHOTOCATALYTIC ACTIVITY OF CdS QUANTUM DOTS SENSITIZED CARBON NANOTUBES (CNTs) NANOCOMPOSITE

NANO ◽  
2014 ◽  
Vol 09 (02) ◽  
pp. 1450017 ◽  
Author(s):  
XINLIN LIU ◽  
YANFENG TANG ◽  
CHANGCHANG MA ◽  
YAN YAN ◽  
PENG LV ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
X Ray Diffraction ◽  
Composite Photocatalyst ◽  
Transmission Electron ◽  
Excellent Photocatalytic Activity ◽  
New Type ◽  
Mechanism And Kinetics ◽  
Kinetics Of

A new-type photocatalyst of cadmium sulfide carbon nanotubes ( CdS /CNTs) was prepared by the hydrothermal method. This as-prepared CdS /CNTs composite photocatalyst was proved to exhibit an excellent photocatalytic activity for degradation of tetracycline (TC). Specially, the 95%- CdS –5%-CNTs composite photocatalyst played the best degradation rate (81.2%) in 60 min under the visible light irradiation. Moreover, this 95%- CdS –5%-CNTs composite photocatalyst possessed great stability and could be used at least four cycles with almost no loss of photocatalytic efficiency. Furthermore, the as-synthesized CdS /CNTs composite photocatalyst was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-Vis diffused reflectance spectra (UV-Vis), Raman and thermal gravimetry (TG). In addition, the possible mechanism and kinetics of photodegradation of TC with CdS /CNTs photocatalyst was also discussed.

SYNTHESIS OF Bi2WO6 MICROSPHERES WITH VISIBLE-LIGHT-DRIVEN PHOTOCATALYTIC PROPERTIES

2013 ◽  
Vol 12 (05) ◽  
pp. 1350035 ◽  
Author(s):  
GENGPING WAN ◽  
GUIZHEN WANG
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Large Scale ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Light Region ◽  
Visible Light Driven ◽  
Uv Visible

Bi 2 WO 6 microspheres constructed from nanosheets have been synthesized by a controllable solvothermal route in a large scale. The structure characterizations of the microspheres were investigated in detail by means of X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). On the basis of XRD analysis and SEM observation of the products at different reaction time periods, a growth mechanism of Bi 2 WO 6 microspheres was proposed. UV-Visible diffuse reflectance (DR) spectrum of the prepared Bi 2 WO 6 microspheres demonstrates that they have absorption in the visible light region. The photocatalytic activity of Bi 2 WO 6 microspheres toward Rhodamine-B ( RhB ) degradation was investigated and the as-prepared products exhibited good photocatalytic activity in degradation of RhB under 300 W Xe lamp light irradiation.

scholarly journals Controlled Synthesis of CuS and Cu9S5 and Their Application in the Photocatalytic Mineralization of Tetracycline

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 899
Author(s):  
Murendeni P. Ravele ◽  
Opeyemi A. Oyewo ◽  
Damian C. Onwudiwe
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Blue Shift ◽  
X Ray Diffraction ◽  
X Ray ◽  
Copper Sulfides ◽  
Transmission Electron ◽  
Single Source Precursor ◽  
Pure Phase ◽  
Pure Phases

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.

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