scholarly journals Preparation and Photocatalytic Property of Ag Modified Titanium Dioxide Exposed High Energy Crystal Plane (001)

Coatings ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 27 ◽  
Author(s):  
Li-Yuan Zhang ◽  
Jia You ◽  
Qian-Wen Li ◽  
Zhi-Hong Dong ◽  
Ya-Jie Zhong ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Absorption Band ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Photocatalytic Property ◽  
High Energy ◽  
Metal Halide ◽  
Crystal Plane ◽  
X Ray ◽  
Metal Halide Lamp

TiO2 exposed high energy crystal plane (001) was prepared by the sol-gel process using butyl titanate as the titanium source and hydrofluoric acid as the surface control agent. Ag-TiO2 was prepared by depositing Ag on the crystal plane of TiO2 (101) with a metal halide lamp. The surface morphology, interplanar spacing, crystal phase composition, ultraviolet absorption band, element composition, and valence state of the samples were characterized by using field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), X-ray diffraction (XRD), ultraviolet-visible absorption spectrum (UV-Vis-Abs), and X-ray photoelectron spectroscopy (XPS), respectively. The formation mechanism of high energy crystal plane (001) was discussed, and the photocatalytic activities were evaluated by following degradation of methyl orange. The results show that TiO2 exposed the (001) crystal plane with a ratio of 41.8%, and Ag can be uniformly deposited on the crystal plane of TiO2 (101) by means of metal halide lamp deposition. Under the same conditions, the degradation rate of methyl orange by deposited Ag-TiO2 reaches as much as 93.63% after 60 min using the metal halide lamp (300 W) as an illuminant, 81.89% by non-deposited samples and 75.20% by nano-TiO2, causing a certain blue shift in the light absorption band edge of TiO2. Ag-TiO2 has the best photocatalytic performance at a pH value of 2.

scholarly journals Preparation and Photocatalytic Properties of CdS/F–TiO2 Composites

Coatings ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 824
Author(s):  
Li-Yuan Zhang ◽  
Jia You ◽  
Qian-Wen Li ◽  
Zhi-Hong Dong ◽  
Ya-Jie Zhong ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Absorption Band ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Methyl Orange Solution ◽  
Precipitation Method ◽  
Order Kinetic ◽  
Visible Absorption ◽  
X Ray ◽  
Titanium Sulfate

F–TiO2 was prepared by a simple precipitation method using titanium sulfate as the titanium source, hydrogen fluoride as the fluorine source and ammonia as the precipitant. CdS/F–TiO2 composites were prepared by hydrothermal synthesis of CdS and F–TiO2. The surface morphology, crystal phase composition, ultraviolet absorption band, fluorescence intensity, element composition, valence state, specific surface and pore structure of the samples were characterized by using field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), ultraviolet visible absorption spectrum (UV-Vis-Abs), Molecular fluorescence spectrophotometer (PL) and X-Ray photoelectron spectroscopy (XPS) and Surface area analyzer (BET), respectively. The effects of the dosage of the photocatalyst, pH value, the concentration of methyl orange and the addition of H2O2 on the photocatalytic performance were investigated with methyl orange solution as the target degradation product. The results showed the optimum condition for photodegradation of methyl orange by 1% CdS/F–TiO2 is that the pH value, the solid-liquid ratio, the concentration of methyl orange and the dosage of H2O2 is 2, 2 g/L, 10 mg/L and 3%, respectively. Under the same conditions, the degradation rate of methyl orange by 1% CdS/F–TiO2 was 93.36% when 300 W metal halide lamp was irradiated for 20 minutes, which was significantly higher than that of F–TiO2. CdS has a significant effect on the morphology, crystallinity, grain size and the compound probability of electrons and holes after the F–TiO2 modification. The composite causes a significant red shift at the edge of the F–TiO2 light absorption band. The photocatalytic degradation of methyl orange by 1% CdS/F–TiO2 follows the Langmuir-Hinshelwood first-order kinetic model.

Effects of Precursor pH Value and Calcination Temperature on Photocatalytic Properties of Ni-Fe Codoped ZnO Nanoparticles

2014 ◽  
Vol 1053 ◽  
pp. 165-172
Author(s):  
Qin Zhang ◽  
Jing Quan Zhang ◽  
Ming Xu ◽  
Chun Lai Zhang ◽  
Cheng Jun Dong ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Photocatalytic Degradation ◽  
Calcination Temperature ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Degradation Mechanism ◽  
Sol Gel ◽  
Precursor Solution ◽  
X Ray ◽  
Zno Powder

(Ni, Fe)-codoped ZnO powder was synthesized by a sol-gel process, using oxalic acid zinc as the zinc source. Effects of the pH value of the precursor solution and the calcination temperature on the photocatalytic degradation efficiency of (Ni, Fe)-codoped ZnO powder were studied by using methyl orange as the degradation object. The structures, morphology and ingredients were characterized by X-ray diffraction, scanning electron microscopy and X-ray photoelectron spectroscopy. The results show that all the samples are polycrystalline with a nanocrystal size of about 20~30nm. The methyl orange solution (8 mg/L) was degraded by more than 50% in 12 hours under the irradiation of natural light in the presence of the (Fe, Ni)-codoped ZnO sample synthesized under these conditions: the doping concentrations of both Ni, Fe are 1%, the pH of the precursor solution is 7.5, and the calcination temperature is 375°C. The photocatalytic degradation mechanism of (Ni, Fe)-codoped ZnO powder is discussed qualitatively, based on the microstructure analysis.

scholarly journals Photocatalytic activity of Cu2O/ZnO nanocomposite for the decomposition of methyl orange under visible light irradiation

2019 ◽  
Vol 26 (1) ◽  
pp. 104-113 ◽  
Author(s):  
Xian-sheng Wang ◽  
Yu-duo Zhang ◽  
Qiao-chu Wang ◽  
Bo Dong ◽  
Yan-jia Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Methyl Orange ◽  
Photoelectron Spectroscopy ◽  
Visible Region ◽  
Methyl Orange Solution ◽  
Degradation Efficiency ◽  
X Ray ◽  
Transmission Electron ◽  
Consistent Performance ◽  
Two Phases

AbstractZnO is modified by Cu2O by the process of precipitation and calcination. X-ray diffraction has shown that Cu2O/ZnO catalysts are made of highly purified cubic Cu2O and hexagonal ZnO. Scanning electron microscopy and transmission electron microscopy have shown that ZnO adhered to the surface of Cu2O. Due to the doping of Cu2O, the absorption range of the Cu2O/ZnO catalyst is shifted from the ultraviolet to the visible region due to diffuse reflection. X-ray photoelectron spectroscopy and photoluminescence spectra have confirmed that there is a substantial interaction between the two phases of the resultant catalyst. The degradation efficiency of Cu2O/ZnO on methyl orange solution is obviously enhanced compared to Cu2O and ZnO. The maximum degradation efficiency is 98%. The degradation efficiency is affected by the pH of the solution and initial concentration. After three rounds of recycling, the degradation rate is almost same. This shows a consistent performance of Cu2O/ZnO. The increase in catalytic ability is related to the lattice interaction caused by the doping of Cu2O.

Characterization of X-ray irradiated graphene oxide coatings using X-ray diffraction, X-ray photoelectron spectroscopy, and atomic force microscopy

2013 ◽  
Vol 28 (2) ◽  
pp. 68-71 ◽  
Author(s):  
Thomas N. Blanton ◽  
Debasis Majumdar
Keyword(s):  
Atomic Force Microscopy ◽  
Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
High Energy ◽  
X Ray Diffraction ◽  
Carbon Phase ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Before And After

In an effort to study an alternative approach to make graphene from graphene oxide (GO), exposure of GO to high-energy X-ray radiation has been performed. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) have been used to characterize GO before and after irradiation. Results indicate that GO exposed to high-energy radiation is converted to an amorphous carbon phase that is conductive.

scholarly journals Aqueous poly(N-Vinylformamide-co-Vinylamine) as a suitable adhesion promoter for wood veneer/biopolyethylene composite materials

BioResources ◽  
2017 ◽  
Vol 12 (4) ◽  
pp. 8134-8159
Author(s):  
Rico John ◽  
Katja Trommler ◽  
Katja Schreiter ◽  
Carolin Siegel ◽  
Frank Simon ◽  
...  
Keyword(s):  
Composite Materials ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Structural Parameters ◽  
Degree Of Hydrolysis ◽  
Adhesion Promoter ◽  
Wood Veneer ◽  
X Ray ◽  
Young’S Moduli ◽  
Veneer Surface

Wood veneer/biopolyethylene (bio-PE) biocomposite materials were produced by using poly(N-vinylformamide-co-vinylamine) (PVFA-co-PVAm) copolymers as a phase-mediating reagent. In a preliminary step, PVFA-co-PVAm was adsorbed onto the wood veneer component from aqueous solution. In its adsorbed form, it served as an adhesion promoter and improved the compatibility between both the highly polar wood veneer and weakly polar bio-PE surface. Structural parameters and their effect on the adsorption process, such as the degree of hydrolysis (DH) of poly(N-vinylformamide) (PVFA) (30, 50, and > 90%), the molecular weight of PVFA-co-PVAm (Mw 10,000, 45,000, or 340,000 g/mol), and the pH value (4, 7, and 11) influenced the resulting wetting behavior of the PVFA-co-PVAm-modified wood veneer surface. Thus, the hydrophobizing effect of the PVFA-co-PVAm was clearly detectable because the contact angle with water was considerably increased up to 116° by adsorption of PVFA-co-PVAm 9095 at pH 11. The adsorbed amount of PVFA-co-PVAm was determined by energy-dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS). The PVFA-co-PVAm-coated wood veneers were consolidated with bio-PE in a hot press process. The modified composite materials showed remarkably improved Young’s moduli (552 MPa) and tensile strengths (4.5 MPa) compared to former composite materials produced without PVFA-co-PVAm modification.

Influence of Ag Doping on the Crystal Structure and Photocatalytic Activity of FeVO4

2011 ◽  
Vol 197-198 ◽  
pp. 919-925 ◽  
Author(s):  
Min Wang ◽  
Qiong Liu
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Photoelectron Spectroscopy ◽  
Methyl Orange Solution ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
X Ray ◽  
Orange Solution ◽  
Decoloration Rate

Silver (Ag+) doped iron (III) vanadate (FeVO4) samples are prepared by the precipitation method and then characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and X-ray photoelectron spectroscopy(XPS). The photocatalytic activity under visible light is evaluated by photocatalytic degradation of methyl orange (MO) in the solution. The results show that both FeVO4 and Ag+ doped FeVO4 samples are triclinic, the later have different surface morphology, and some needle-shaped materials appear in the later. From XPS, there are more Fe2+ ions in Ag+ doped FeVO4 sample than that in FeVO4 one without Ag+. It indicates that Ag+ doping can increase the density of the surface oxygen vacancies of catalysts, which can act as electron traps promoting the electron-hole separation and then increase the photo-activity. The decoloration rate after Ag+ doping against methyl orange solution can reach about 81%, and be more about 20％ than that of pure FeVO4.

Interface Characterization of PbTe/BaSi/Si Heterostructures Grown Using MBE

1992 ◽  
Vol 281 ◽  
Author(s):  
F. Santiago ◽  
D. Woody ◽  
T. K. Chu ◽  
C. A. Huber
Keyword(s):  
Photoelectron Spectroscopy ◽  
High Energy ◽  
Substrate Material ◽  
Interfacial Region ◽  
X Ray ◽  
Interface Characterization ◽  
Spectroscopy Studies ◽  
Molecular Layers ◽  
Similar Growth

ABSTRACTA new substrate material consisting of a buffer layer of a Ba-Si compound was developed by making use of the chemical reaction between BaF2 and Si. This substrate is very promising for the integration of IV-VI semiconductor materials with silicon. PbTe films of excellent quality, as determined by X-ray and Reflected High Energy Electron Diffraction spectra, have been deposited over (111)- and (100)-oriented silicon wafers of 3 inch diameter. These PbTe films are (100)-oriented irrespective of the Si orientation. X-ray photoelectron spectroscopy studies reveal very interesting chemistry at the interface between Ba-Si and Te. They suggest that BaTe may form between PbTe and Ba-Si at their interface. This interfacial region, which is of the order of only a few molecular layers, appears to be critical in the success of the deposition. Thermal cycling showed that the PbTe/BaSi/Si system is mechanically very stable. The possibility of a similar growth mechanism for the deposition of II-VI semiconductors such as CdTe is considered.

scholarly journals Mechanochemically Synthesised Coal-Based Magnetic Carbon Composites for Removing As(V) and Cd(II) from Aqueous Solutions

Nanomaterials ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 100 ◽  
Author(s):  
Anton Zubrik ◽  
Marek Matik ◽  
Michal Lovás ◽  
Zuzana Danková ◽  
Mária Kaňuchová ◽  
...  
Keyword(s):  
Mössbauer Spectroscopy ◽  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Mossbauer Spectroscopy ◽  
Nitrogen Adsorption ◽  
High Energy ◽  
Magnetic Composites ◽  
Responsive Materials ◽  
X Ray ◽  
Mößbauer Spectroscopy

The continued decrease in water quality requires new advances in the treatment of wastewater, including the preparation of novel, effective, environmentally friendly, and affordable sorbents of toxic pollutants. We introduce a simple non-conventional mechanochemical synthesis of magnetically responsive materials. Magnetic lignite and magnetic char were prepared by high-energy ball co-milling from either raw Slovak lignite or coal-based char together with a ferrofluid. The products were characterised by X-ray diffraction, electron microscopy, 57Fe Mössbauer spectroscopy, X-ray photoelectron spectroscopy (XPS), volumetric magnetic susceptibility, and low-temperature nitrogen adsorption, and both magnetic carbons were comparatively tested as potential sorbents of As(V) oxyanions and Cd(II) cations in aqueous solutions. The magnetic char was an excellent sorbent of As(V) oxyanions (Qm = 19.9 mg/g at pH 3.9), whereas the magnetic lignite was less effective. The different sorption properties towards arsenic anions may have been due to different oxidation states of iron on the surfaces of the two magnetic composites (determined by XPS), although the overall state of iron monitored by Mössbauer spectroscopy was similar for both samples. Both magnetic composites were effective sorbents for removing Cd(II) cations (Qm (magnetic lignite) = 70.4 mg/g at pH 6.5; Qm (magnetic char) = 58.8 mg/g at pH 6.8).

scholarly journals Efficient Flexible All-Solid Supercapacitors with Direct Sputter-Grown Needle-Like Mn/MnOx@Graphite-Foil Electrodes and PPC-Embedded Ionic Electrolytes

Nanomaterials ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1768
Author(s):  
Apurba Ray ◽  
Delale Korkut ◽  
Bilge Saruhan
Keyword(s):  
Solid State ◽  
Photoelectron Spectroscopy ◽  
Electrode Materials ◽  
High Energy ◽  
Polymer Gel ◽  
Graphite Foil ◽  
Polymer Gel Electrolyte ◽  
X Ray ◽  
Long Cycle ◽  
Capacitance Performance

Recent critical issues regarding next-generation energy storage systems concern the cost-effective production of lightweight, safe and flexible supercapacitors yielding high performances, such as high energy and power densities as well as a long cycle life. Thus, current research efforts are concentrated on the development of high-performance advance electrode materials with high capacitance and excellent stability and solid electrolytes that confer flexibility and safety features. In this work, emphasis is placed on the binder-free, needle-like nanostructured Mn/MnOx layers grown onto graphite-foil deposited by reactive sputtering technique and to the polymer gel embedded ionic electrolytes, which are to be employed as new flexible pseudocapacitive supercapacitor components. Microstructural, morphological and compositional analysis of the layers has been investigated by X-ray diffractometer (XRD), Field Emission Scanning Electron Microscope (FE–SEM) and X-ray photoelectron spectroscopy (XPS). A flexible lightweight symmetric pouch-cell solid-state supercapacitor device is fabricated by sandwiching a PPC-embedded ionic liquid ethyl-methylimidazolium bis (trifluoromethylsulfonyl) imide (EMIM)(TFSI) polymer gel electrolyte (PGE) between two Mn/MnOx@Graphite-foil electrodes and tested to exhibit promising supercapacitive behaviour with a wide stable electrochemical potential window (up to 2.2 V) and long-cycle stability. This pouch-cell supercapacitor device offers a maximum areal capacitance of 11.71 mF/cm2@ 0.03 mA/cm2 with maximum areal energy density (Ea) of 7.87 mWh/cm2 and areal power density (Pa) of 1099.64 mW/cm2, as well as low resistance, flexibility and good cycling stability. This supercapacitor device is also environmentally safe and could be operated under a relatively wide potential window without significant degradation of capacitance performance compared to other reported values. Overall, these rationally designed flexible symmetric all-solid-state supercapacitors signify a new promising and emerging candidate for component integrated storage of renewable energy harvested current.

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