scholarly journals Fabrication and Photocatalytic Property of One-Dimensional SrTiO3/TiO2-xNxNanostructures

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Huarong Zhang ◽  
Miao Guashuai ◽  
Ma Xingping ◽  
Wang Bei
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Photocatalytic Property ◽  
Titanate Nanotubes ◽  
Mixed Solution ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Transmission Electron ◽  
Property Changes

One-dimensional SrTiO3/TiO2−xNxnanostructures were prepared by the hydrothermal method and investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS) measurements. The photocatalytic activities of the prepared samples were evaluated by photodegrading the methylene blue (MB) solution. According to the characterizations, the intermediate product of SrTiO3/titanate nanotubes was presented after hydrothermal processing of the TiO2−xNxnanoparticles with the mixed solution of NaOH and Sr(NO3)2. The final product of SrTiO3/TiO2−xNxnanorods was obtained after calcining the intermediate. As compared to the TiO2−xNxnanoparticles, the absorption performance of SrTiO3/titanate nanotubes or SrTiO3/TiO2−xNxnanorods was depressed, instead of improving it. The mechanisms of the absorption property changes were discussed. The SrTiO3/TiO2−xNxnanorods presented better photocatalytic activity than the TiO2−xNxnanoparticles or nanorods. However, due to overmuch adsorption, the SrTiO3/titanate nanotubes gave ordinary photocatalytic performances.

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.

scholarly journals Improved Visible Light Photocatalytic Activity for TiO2Nanomaterials by Codoping with Zinc and Sulfur

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Qianzhi Xu ◽  
Xiuying Wang ◽  
Xiaoli Dong ◽  
Chun Ma ◽  
Xiufang Zhang ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Sunlight Irradiation ◽  
X Ray ◽  
Transmission Electron ◽  
Photoinduced Charge

S/Zn codoped TiO2nanomaterials were synthesized by a sol-gel method. X-ray diffraction, UV-vis diffuse reflectance spectroscopy, transmission electron microscopy, photoluminescence spectroscopy, and X-ray photoelectron spectroscopy were used to characterize the morphology, structure, and optical properties of the prepared samples. The introduction of Zn and S resulted in significant red shift of absorption edge for TiO2-based nanomaterials. The photocatalytic activity was evaluated by degrading reactive brilliant red X-3B solution under simulated sunlight irradiation. The results showed S/Zn codoped TiO2exhibited higher photocatalytic activity than pure TiO2and commercial P25, due to the photosynergistic effect of obvious visible light absorption, efficient separation of photoinduced charge carriers, and large surface area. Moreover, the content of Zn and S in the composites played important roles in photocatalytic activity of TiO2-based nanomaterials.

scholarly journals Au/TiO2Reusable Photocatalysts for Dye Degradation

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Silija Padikkaparambil ◽  
Binitha Narayanan ◽  
Zahira Yaakob ◽  
Suraja Viswanathan ◽  
Siti Masrinda Tasirin
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Diffuse Reflectance Spectroscopy ◽  
Dye Degradation ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron ◽  
Uv Visible

Nanogold doped TiO2catalysts are synthesized, and their application in the photodegradation of dye pollutants is studied. The materials are characterized using different analytical techniques such as X-ray diffraction, transmission electron microscopy, UV-visible diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy. The results revealed the strong interaction between the metallic gold nanoparticles and the anatase TiO2support. Au doped systems showed very good photoactivity in the degradation of dye pollutants under UV irradiation as well as in sunlight. A simple mechanism is proposed for explaining the excellent photoactivity of the systems. The reusability studies of the photocatalysts exhibited more than 98% degradation of the dye even after 10 repeated cycles.

A Facile Synthesis of CuInS2 Nanoparticles from Molecular Single Source Precursors

2007 ◽  
Vol 7 (12) ◽  
pp. 4353-4364 ◽  
Author(s):  
Dimple P. Dutta ◽  
Garima Sharma ◽  
A. K. Tyagi
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Optical Band Gap ◽  
Diffuse Reflectance Spectroscopy ◽  
Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron

CuInS2 nanoparticles have been synthesized via solvent thermolysis of novel bimetallic complexes of the general formula [(Ph3P)2 CuIn(S2COR)4] (where R = CH3; C2H5; C(CH3)2; and [(Ph3P)2 CuIn(SCH2CH2S)2]. These complexes have been prepared by the reactions of Na/KS2 COR and NaSCH2 CH2 SNa with InCl3 and [(Ph3 P)2 CuNO3] in methanol, respectively. Solvent thermolyses of these complexes were carried out in ethylene glycol at 196 °C for different time periods. The nanoparticles obtained were characterized extensively by techniques like powder X-ray diffraction, transmission electron microscopy, selected area electron diffraction, and X-ray photoelectron spectroscopy. The optical band gap of the nanoparticles was determined by diffuse reflectance spectroscopy (DRS).

scholarly journals Comparative Study of the Photocatalytic Hydrogen Evolution over Cd1−xMnxS and CdS-β-Mn3O4-MnOOH Photocatalysts under Visible Light

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 355
Author(s):  
Ksenia O. Potapenko ◽  
Anna Yu. Kurenkova ◽  
Andrey V. Bukhtiyarov ◽  
Evgeny Yu. Gerasimov ◽  
Svetlana V. Cherepanova ◽  
...  
Keyword(s):  
Solid Solution ◽  
Visible Light ◽  
Hydrogen Evolution ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Diffraction Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Manganese Salts

A series of solid solutions of cadmium and manganese sulfides, Cd1−xMnxS (x = 0–0.35), and composite photocatalysts, CdS-β-Mn3O4-MnOOH, were synthesized by precipitation with sodium sulfide from soluble cadmium and manganese salts with further hydrothermal treatment at 120 °C. The obtained photocatalysts were studied by the X-ray diffraction method (XRD), UV-vis diffuse reflectance spectroscopy, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and N2 low temperature adsorption. The photocatalysts were tested in hydrogen production using a Na2S/Na2SO3 aqueous solution under visible light (λ = 450 nm). It was shown for the first time that both kinds of photocatalysts possess high activity in hydrogen evolution under visible light. The solid solution Cd0.65Mn0.35S has an enhanced photocatalytic activity due to its valence and conduction band position tuning, whereas the CdS-β-Mn3O4-MnOOH (40–60 at% Mn) samples were active due to ternary heterojunction formation. Further, the composite CdS-β-Mn3O4-MnOOH photocatalyst had much higher stability in comparison to the Cd0.65Mn0.35S solid solution. The highest activity was 600 mmol g−1 h−1, and apparent quantum efficiency of 2.9% (λ = 450 nm) was possessed by the sample of CdS-β-Mn3O4-MnOOH (40 at% Mn).

Dye-Sensitized-Assisted, Enhanced Photocatalytic Activity of TiO2/Bi4V2O11

NANO ◽  
2018 ◽  
Vol 13 (03) ◽  
pp. 1850028 ◽  
Author(s):  
Mengjun Liang ◽  
Zhiyuan Yang ◽  
Ying Mei ◽  
Haoran Zhou ◽  
Shuijin Yang
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Sensitized ◽  
Transmission Electron ◽  
Efficient Charge ◽  
Degradation Activity ◽  
Adsorption Desorption

In this study, the TiO2/Bi4V2O[Formula: see text] nanocomposite photocatalysts were prepared by loading different amount of TiO2 nanoparticles onto the surface of Bi4V2O[Formula: see text] nanospheres via a facile hydrothermal method. Afterwards, the as-synthesized samples were characterized by high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), N2 adsorption–desorption isotherms, X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS) and photocurrent techniques. The optimal TiO2/Bi4V2O[Formula: see text] composite with 20[Formula: see text]wt.% TiO2 loading (TB2) exhibited the best photocatalytic activity, which could degrade almost RhB completely within 30[Formula: see text]min under visible light irradiation. The enhanced photocatalytic activity of TiO2/Bi4V2O[Formula: see text] composites for RhB degradation could be mainly ascribed to the efficient charge separation over dye-induced sensitized and the increased specific surface area. Also, the photocatalytic activities of TiO2/Bi4V2O[Formula: see text] for CIP degradation were tested. After five consecutive recycling experiments, the photocatalytic degradation activity of TB2 could still reach 99% which indicated that the catalysts had superior stability. Based on the experimental and bandgap calculations, a possible photocatalytic mechanism of TiO2/Bi4V2O[Formula: see text] for RhB degradation was proposed.

scholarly journals A Facile Synthesis of Graphene-WO3Nanowire Clusters with High Photocatalytic Activity for O2Evolution

2014 ◽  
Vol 2014 ◽  
pp. 1-6
Author(s):  
M.-J. Zhou ◽  
N. Zhang ◽  
Z. H. Hou
Keyword(s):  
Photocatalytic Activity ◽  
Water Splitting ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Charge Transfer Rate ◽  
Ft Ir

In the present work, graphene-WO3nanowire clusters were synthesizedviaa facile hydrothermal method. The obtained graphene-WO3nanowire clusters were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, and ultraviolet-visible diffuse reflectance spectroscopy (DRS) techniques. The photocatalytic oxygen (O2) evolution properties of the as-synthesized samples were investigated by measuring the amount of evolved O2from water splitting. The graphene-WO3nanowire clusters exhibited enhanced performance compared to pure WO3nanowire clusters for O2evolution. The amount of evolved O2from water splitting after 8 h for the graphene-WO3nanowire clusters isca.0.345 mmol/L, which is more than 1.9 times as much as that of the pure WO3nanowire clusters (ca.0.175 mmol/L). The high photocatalytic activity of the graphene-WO3nanowire clusters was attributed to a high charge transfer rate in the presence of graphene.

Solid-Phase Synthesis and Photocatalytic Property of Cobalt-Doped TiO2 Mesoporous Materials

2011 ◽  
Vol 217-218 ◽  
pp. 1462-1468 ◽  
Author(s):  
Shao You Liu ◽  
Qing Ge Feng
Keyword(s):  
Photoelectron Spectroscopy ◽  
Solid Phase ◽  
Photocatalytic Property ◽  
Textural Properties ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
Bending Vibration ◽  
Toluene Oxidation ◽  
X Ray ◽  
Transmission Electron

Mesoporous cobalt-doped TiO2 (Co-TiO2) material has been synthesized by solid-state reaction route. The textural properties of the samples are monitored by the X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM) and energy dispersive spectroscopy(EDS), Raman spectroscopy, N2-physisorption, Fourier transform infrared spectroscopy (FT-IR), ultraviolet visible light spectroscopy (UV-Vis) and X-ray photoelectron spectroscopy(XPS). It is shown that the mesoporous Co-TiO2 is consisted of polycrystalline with some amorphous mixture and trace cobalt oxide. Cobalt has been incorporated into the framework of anatase TiO2. The bending vibration at 1124 cm-1 of Co-O-Ti bond in mesoporous Co-TiO2 material is confirmed. Interestingly, it possesses a large BET surface area (97.6 m2/g) and a narrow distribution of pore size presenting a better photocatalytic reactivity for toluene oxidation. Within 150 min irradiation, the maximum conversion (95 mol%) of toluene oxidation is obtained.

scholarly journals Platinum-Decorated TiO2: One Step Fast Monometallic Impregnation and Plasma Effect on Nanoparticles

2021 ◽  
Vol 6 (1) ◽  
pp. 4
Author(s):  
Rudy Trejo-Tzab ◽  
Alejandro Avila-Ortega ◽  
Patricia Quintana-Owen ◽  
Ricardo Rangel ◽  
Mayra Angélica Álvarez-Lemus
Keyword(s):  
Platinum Nanoparticles ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Plasma Discharge ◽  
Nitrogen Plasma ◽  
X Ray Diffraction ◽  
Discharge System ◽  
X Ray ◽  
Transmission Electron ◽  
One Step

In the present work, N-TiO2−x/Pt was synthesized using a homemade nitrogen plasma (AC) discharge system. The overall procedure use of low-power nitrogen plasma (100 watts) with 1 and 2 h of plasma discharge to successfully impregnate platinum nanoparticles on P25 titanium dioxide. The obtained samples were characterized using X-ray diffraction (XRD), UV–Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy (HRTEM). The results reveal the incorporation of metallic Pt up to 2.9% on the surface of TiO2 by increasing the duration of plasma discharge by up to two hours with a constant power of 100 watts. Likewise, the incorporation of nitrogen atoms into a lattice crystal was also favored, confirming a direct relationship between the amount of Pt and nitrogen atoms introduced in TiO2 as a function of the duration of plasma treatment. By characterizing nanoparticles loaded on a N-TiO2−x/Pt surface, we show that joined platinum nanoparticles have two different patterns, and the boundary between these two regions coalesces. The results demonstrate that the use of nitrogen plasma to impregnate platinum nanoparticles on the surface of TiO2 to obtain N-TiO2−x/Pt allows wide and relevant physics and chemistry applications.

scholarly journals α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  
Keyword(s):  
Enzyme Immobilization ◽  
Photoelectron Spectroscopy ◽  
Cellulose Fibers ◽  
Relative Activity ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Laccase Immobilization ◽  
Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

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