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

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.

2020 ◽  
Vol 10 ◽  
pp. 184798042090542 ◽  
Author(s):  
R Trejo-Tzab ◽  
JA Aguilar-Jiménez ◽  
P Quintana-Owen ◽  
Alejandro Ávila-Ortega ◽  
MA Alvarez-Lemus ◽  
...  

The main motivation of this work is to deposit two different metals (gold and silver) on titanium oxide nanoparticles surface in a one-step simple and fast physical process by applying a nitrogen plasma as the main source of nitrogen atoms to obtain nanostructured N-TiO2 − X/Au/Ag materials. The obtained nanomaterials were characterized by X-ray photoelectron spectroscopy, X-ray diffraction, diffuse reflectance spectroscopy, scanning electron microscopy–energy dispersive X-ray spectroscopy, and high-resolution transmission electron microscopy. Based on the characterization results, we found that gold and silver nanoparticles were uniformly loaded on the titanium oxide nanocomposite surface, showing a surface plasmon absorption band due to the loading of the metal nanoparticles over titania samples. The results of this work have shown that nitrogen plasma technique is a more feasible and simple alternative to obtain the N-TiO2 − X/Au/Ag nanocomposite. Moreover, this plasma technique could be used to impregnate with other kind of metals over the surface of diverse nanomaterials.


2012 ◽  
Vol 2012 ◽  
pp. 1-12 ◽  
Author(s):  
Jiang Zhang ◽  
Zheng-Hong Huang ◽  
Yong Xu ◽  
Feiyu Kang

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.


2020 ◽  
Vol 98 (12) ◽  
pp. 771-778
Author(s):  
Xin Chang ◽  
Xiangyang Xu ◽  
Zhifeng Gao ◽  
Yingrui Tao ◽  
Yixuan Yin ◽  
...  

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.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Qianzhi Xu ◽  
Xiuying Wang ◽  
Xiaoli Dong ◽  
Chun Ma ◽  
Xiufang Zhang ◽  
...  

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.


2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Silija Padikkaparambil ◽  
Binitha Narayanan ◽  
Zahira Yaakob ◽  
Suraja Viswanathan ◽  
Siti Masrinda Tasirin

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.


2014 ◽  
Vol 496-500 ◽  
pp. 297-300 ◽  
Author(s):  
Bi Tao Liu ◽  
Liang Liang Tian ◽  
Ling Ling Peng

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.


2007 ◽  
Vol 7 (12) ◽  
pp. 4353-4364 ◽  
Author(s):  
Dimple P. Dutta ◽  
Garima Sharma ◽  
A. K. Tyagi

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).


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 355
Author(s):  
Ksenia O. Potapenko ◽  
Anna Yu. Kurenkova ◽  
Andrey V. Bukhtiyarov ◽  
Evgeny Yu. Gerasimov ◽  
Svetlana V. Cherepanova ◽  
...  

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).


NANO ◽  
2018 ◽  
Vol 13 (03) ◽  
pp. 1850028 ◽  
Author(s):  
Mengjun Liang ◽  
Zhiyuan Yang ◽  
Ying Mei ◽  
Haoran Zhou ◽  
Shuijin Yang

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.


2020 ◽  
Vol 11 ◽  
pp. 1546-1555
Author(s):  
Juan Rizo ◽  
David Díaz ◽  
Benito Reyes-Trejo ◽  
M Josefina Arellano-Jiménez

Methyl parathion (MP) is one of the most neurotoxic pesticides. An inexpensive and reliable one-step degradation method of MP was achieved through an aqueous suspension of copper(I) oxide nanoparticles (NPs). Three different NPs sizes (16, 29 and 45 nm), determined with X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM), were synthesized using a modified Benedict’s reagent. 1H nuclear magnetic resonance (NMR) results show that the hydrolytic degradation of MP leads to the formation of 4-nitrophenol (4-NPh) as the main product. While the P=S bond of MP becomes P=O, confirmed by 31P NMR. Although Cu2O is a widely known photocatalyst, the degradation of methyl parathion was associated to the surface basicity of Cu2O NPs. Indirect evidence for the basicity of Cu2O NPs was achieved through UV–vis absorption of 4-NPh. Likewise, it was shown that the surface basicity increases with decreasing nanoparticle size. The presence of CuCO3 on the surface of Cu2O, identified using X-ray photoelectron spectroscopy (XPS), passivates its surface and consequently diminishes the degradation of MP.


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