Photocatalytic Performance of BiOCl Nanosheets Composite with Graphene

2014 ◽  
Vol 496-500 ◽  
pp. 297-300 ◽  
Author(s):  
Bi Tao Liu ◽  
Liang Liang Tian ◽  
Ling Ling Peng
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
One Step ◽  
High Migration

A series of composites of the high photoactivity of {001} facets exposed BiOCl and grapheme sheets (GS) were synthesized via a one-step hydrothermal reaction. The obtained BiOCl/GS photocatalysts were characterized by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy, transmission electron microscopy (TEM), Ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy. The as-prepared BiOCl/GS photocatalyst showed enhanced photocatalytic activity for the degradation of methyl orange (MO) under UV and visible light (λ > 400 nm). The enhanced photocatalytic activity could be attributed to oxygen vacancies of the {001} facets of BiOCl/GS and the high migration efficiency of photo-induced electrons, which could suppress the charge recombination effectively.

scholarly journals AgBr/(Sr0.6Bi0.305)2Bi2O7 Heterostructured Composites: Fabrication, Characterization, and Significantly Enhanced Photocatalytic Activity

Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 394 ◽  
Author(s):  
Xinling Wang ◽  
Di Zhu ◽  
Yan Zhong ◽  
Dianhui Wang ◽  
Chaohao Hu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Precipitation Method ◽  
Light Illumination ◽  
X Ray ◽  
Transmission Electron ◽  
Pyrochlore Type

The pyrochlore-type (Sr0.6Bi0.305)2Bi2O7 (SBO) containing Bi3+ and Bi5+ mixed valent states was first investigated as a photocatalyst in our very recent work. To further improve the photocatalytic performance, AgBr/SBO heterostructured composites were synthesized by using a deposition-precipitation method. The characterization of phase structure, morphology, microstructure, elemental composition, and optical properties of the obtained products were performed using X-ray diffractometer (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM)TEM, X-ray photoelectron spectroscopy (XPS), UV-visible diffuse reflectance spectroscopy (UV-vis DRS). The photocatalytic activity of samples was evaluated by degrading methylene blue under visible light illumination. AgBr/SBO composites possess high stability and significantly enhanced photocatalytic performance. The improvement of photocatalytic activity is due to the enhanced light absorption and the separation of photoinduced electrons and holes on the interface of AgBr/SBO heterostructured composites.

In situ Synthesis of p–n LaFeO3/ZnIn2S4 Heterojunctions for Enhanced Photocatalytic Activity

NANO ◽  
2019 ◽  
Vol 14 (08) ◽  
pp. 1950096 ◽  
Author(s):  
Wen Gao ◽  
Chengjia Zhang ◽  
Sainan Cui ◽  
Qian Liang ◽  
Song Xu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
In Situ Synthesis ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Ft Ir ◽  
Composition Structure

In this study, LaFeO3/ZnIn2S4 composites were synthesized via in situ synthesis. The composition, structure and optical absorption properties of LaFeO3/ZnIn2S4 were characterized by X-ray diffraction (XRD), ultraviolet-visible diffuse reflectance spectroscopy, fluorescence spectroscopy (PL), Fourier Transform infrared spectroscopy (FT-IR) and field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM). The photocatalytic activity of the LaFeO3/ZnIn2S4 photocatalyst was determined based on the degradation of methyl orange (MO). LaFeO3/ZnIn2S4 composites showed much better photocatalytic performance compared with pure LaFeO3 and ZnIn2S4. The enhanced photocatalytic performance was attributed to intimately contacted interfaces and charge transfer channels which can effectively transfer and separate the photogenerated charge carriers.

Synthesis and Characterization of Titanium Dioxide Nanotubes for Photocatalytic Degradation of Aqueous Nitrobenzene in the Presence of Sunlight

2010 ◽  
Vol 657 ◽  
pp. 62-74 ◽  
Author(s):  
Rajesh J. Tayade ◽  
D.L. Key
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Tio2 Nanotubes ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
Titanium Dioxide Nanotubes ◽  
X Ray ◽  
Tio2 Anatase ◽  
Transmission Electron

TiO2 derived nanotubes were prepared by hydrothermal treatment of TiO2 (anatase) powder in 10 M NaOH aqueous solution. The crystalline structure, band gap, and morphology of the TiO2 nanotubes were determined by X-ray diffraction (XRD), diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), Transmission Electron microscopy (TEM) and N2 adsorption (BET) at 77 K, respectively. It was observed that the surface area of the nanotubes was increased twelve times compared with TiO2 (anatase) powder. The results demonstrated that the photocatalytic activity of TiO2 nanotubes was higher than that of TiO2 (anatase) powder. The photocatalytic activity of the nanotubes was evaluated in presence of sunlight by degradation of aqueous nitrobenzene. Complete degradation of nitrobenzene was obtained in 4 hours using TiO2 nanotubes whereas 85% degradation was observed in case of TiO2 (anatase).

scholarly journals One-Step Synthesis of b-N-TiO2/C Nanocomposites with High Visible Light Photocatalytic Activity to Degrade Microcystis aeruginosa

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 579
Author(s):  
Xu Zhang ◽  
Min Cai ◽  
Naxin Cui ◽  
Guifa Chen ◽  
Guoyan Zou ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Chlorophyll A ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Transmission Electron ◽  
One Step

Black TiO2 with doped nitrogen and modified carbon (b-N-TiO2/C) were successfully prepared by sol-gel method in the presence of urea as a source of nitrogen and carbon. The photocatalysts were characterized by field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman, electron paramagnetic resonance (EPR), and UV-vis diffuse reflectance spectra (DRS). The doped nitrogen, introduced defects, and modified carbon played a synergistic role in enhancing photocatalytic activity of b-N-TiO2/C for the degradation of chlorophyll-a in algae cells. The sample, with a proper amount of phase composition and oxygen vacancies, showed the highest efficiency to degrade chlorophyll-a, and the addition of H2O2 promoted this photocatalysis degradation. Based on the trapping experiments and electron spin resonance (ESR) signals, a photocatalytic mechanism of b-N-TiO2/C was proposed. In the photocatalytic degradation of chlorophyll-a, the major reactive species were identified as OH and O2−. This research may provide new insights into the photocatalytic inactivation of algae cells by composite photocatalysts.

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.

scholarly journals Hydrothermal Synthesis of Iodine-Doped Nanoplates with Enhanced Visible and Ultraviolet-Induced Photocatalytic Activities

2012 ◽  
Vol 2012 ◽  
pp. 1-12 ◽  
Author(s):  
Jiang Zhang ◽  
Zheng-Hong Huang ◽  
Yong Xu ◽  
Feiyu Kang
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Oxygen Vacancies ◽  
Diffuse Reflectance Spectroscopy ◽  
Synergetic Effect ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Photocatalytic Activities

The iodine-doped Bi2WO6(I-BWO) photocatalyst was prepared via a hydrothermal method using potassium iodide as the source of iodine. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of I-BWO for the degradation of rhodamine B (RhB) was higher than that of pure BWO and I2-BWO regardless of visible light (>420 nm) or ultraviolet light (<400 nm) irradiation. The results of DRS analysis showed that the I-BWO and I2-BWO catalysts had narrower band gaps. XPS analysis proved that the multivalent iodine species including I0and were coadsorbed on the defect surface of Bi2WO6in I-BWO. The enhanced PL intensity revealed that a large number of defects of oxygen vacancies were formed by the doping of iodine. The enhanced photocatalytic activity of I-BWO for degradation of RhB was caused by the synergetic effect of a small crystalline size, a narrow band gap, and plenty of oxygen vacancies.

Evolution of Crystalline Phase and Morphology of the Products Formed during the Hydrothermal Synthesis of Y2O3 Powders

2011 ◽  
Vol 189-193 ◽  
pp. 1275-1279
Author(s):  
Ying Wang ◽  
Gao Yang Zhao ◽  
Li Yuan
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Treatment ◽  
Crystalline Phase ◽  
Hydrothermal Reaction ◽  
Yttrium Nitrate ◽  
Temperature Reaction ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron

The crystalline phase and morphology of the products formed during the synthesis of yttrium oxide via the hydrothermal treatment yttrium nitrate were characterized by X-ray diffraction, transmission electron microscopy and scanning electron microscopy. Products with high OH/NO3ratios are formed with the increasing of hydrothermal treatment. The crystalline phases are evolved from Y2(OH)5.14(NO3)0.86•H2O toY4O(OH)9(NO3) and finally Y(OH)3. The hydrothermal reaction conditions play an important role in the synthesis of the microstructures. Results show the particle size and final morphology of samples could be controlled by reaction temperature, reaction time, and OH-concentration. Sheets, hexagonal and needle-like Y2O3powders are obtained with the hydrothermal treatment of yittrium nitrate at 180 oC to 200oC for 2-8 hours at pH 9-13.

scholarly journals A facile synthesis of a carbon-encapsulated Fe3O4 nanocomposite and its performance as anode in lithium-ion batteries

2013 ◽  
Vol 4 ◽  
pp. 699-704 ◽  
Author(s):  
Raju Prakash ◽  
Katharina Fanselau ◽  
Shuhua Ren ◽  
Tapan Kumar Mandal ◽  
Christian Kübel ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Lithium Ion ◽  
Iron Pentacarbonyl ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Lithium Ion Cell ◽  
Carbon Framework ◽  
One Step

A carbon-encapsulated Fe3O4 nanocomposite was prepared by a simple one-step pyrolysis of iron pentacarbonyl without using any templates, solvents or surfactants. The structure and morphology of the nanocomposite was investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer–Emmett–Teller analysis and Raman spectroscopy. Fe3O4 nanoparticles are dispersed intimately in a carbon framework. The nanocomposite exhibits well constructed core–shell and nanotube structures, with Fe3O4 cores and graphitic shells/tubes. The as-synthesized material could be used directly as anode in a lithium-ion cell and demonstrated a stable capacity, and good cyclic and rate performances.

Activation of persulfate by heterogeneous catalyst ZnCo2O4–RGO for efficient degradation of bisphenol A

2020 ◽  
Vol 98 (12) ◽  
pp. 771-778
Author(s):  
Xin Chang ◽  
Xiangyang Xu ◽  
Zhifeng Gao ◽  
Yingrui Tao ◽  
Yixuan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Bisphenol A ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Nucleation Sites ◽  
One Step ◽  
Application Potential

A nanocomposite, reduced graphene oxide (RGO) modified ZnCo2O4 (ZnCo2O4–RGO) was synthesized via one-step solvothermal method for activating persulfate (PS) to degrade bisphenol A (BPA). The morphology and structure of the nanocomposite were identified by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. RGO provides nucleation sites for ZnCo2O4 to grow and inhibits the agglomeration of the nanoparticles. The influence of different reaction conditions on the oxidation of BPA catalyzed by ZnCo2O4–RGO was investigated, including the content of RGO, the dosage of catalyst, the concentration of humic acid (HA), anions in the environment, the reaction temperature, and pH. BPA can be totally degraded within 20 min under optimized reaction conditions. The presence of HA, Cl−, and NO3− only has a slight effect on the oxidation of BPA, whereas the presence of either H2PO4− or HCO3− can greatly inhibit the reaction. ZnCo2O4–RGO shows good cycling stability and practical application potential. A reaction mechanism of the degradation of BPA was also explored.

scholarly journals Hydrothermal Synthesis of rGO/PbTiO3 Photocatalyst and Its Photocatalytic H2 Evolution Activity

2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Chunyan Wang ◽  
Lianwei Shan ◽  
Dongyuan Song ◽  
Yanwei Xiao ◽  
Jagadeesh Suriyaprakash
Keyword(s):  
Photocatalytic Performance ◽  
H2 Evolution ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Efficient Charge ◽  
One Step ◽  
Photocatalytic H2 Evolution

In this letter, we investigated the photocatalytic activity of the newly formed rGO/PbTiO3 composites, which are synthesized by a one-step hydrothermal route. By adjusting the amount of reduced graphene oxide (rGO) (0, 0.15, 0.30, 0.60, and 1.20 wt%) with the PbTiO3, we constructed various photocatalysts for this investigation. The crystal structure and morphology of the various composites were studied by powder X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Photoelectron spectroscopic study revealed that the band structure of the newly formed composites and efficient charge separation can be obtained by the interfaces of various rGO content. In addition, the photocatalytic performance of the synthesized composites was explored by H2 evolution and rhodamine blue (RhB) degradation. The obtained results indicated that the addition of the appropriate amount of rGO could improve the activity of pure PbTiO3, significantly.

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