Synthesis and photophysical properties of barium indium oxides

2002 ◽  
Vol 17 (9) ◽  
pp. 2201-2204 ◽  
Author(s):  
J. Yin ◽  
Z. Zou ◽  
J. Ye

Barium indium oxides (BaIn2O4, Ba4In6O13, Ba2In2O5, Ba3In2O6, and Ba5In2O8) were synthesized by the citric process and characterized by powder x-ray diffraction. The optical absorption properties of these compounds were investigated by UV–visible diffuse reflectance spectroscopy. It was found that with the increase of the mole ratio of In2O3 in the formula the optical absorption edges of these oxides shift to the longer wavelength side monotonically. The photocatalytic H2 and O2 evolutions under visible light irradiation (λ > 420 nm) from aqueous CH3OH/H2O and AgNO3/H2O solutions were performed. Among these oxides, BaIn2O4 was the most stable compound, and other compounds were not stable chemically in the case of water and visible light irradiation.

2014 ◽  
Vol 787 ◽  
pp. 35-40 ◽  
Author(s):  
Xiao Yan Zhou ◽  
Peng Wei Zhou ◽  
Hao Guo ◽  
Bo Yang ◽  
Ru Fei Ren

The p-n junction photocatalysts, p-CuO (at. 0-25%)/n-ZnO nanocomposite were prepared through hydrothermal method without using any organic solvent or surfactant. The as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-Ray spectroscopy, and UV-vis spectroscopy. The results demonstrated that the CuO/ZnO nanocomposite presented a two-dimensional morphology composed of sheet-like ZnO nanostructures adorned with CuO nanoparticles. The photocatalytic activity of CuO/ZnO with different Cu/Zn molar rations and pure ZnO synthesized by the identical synthetic route were evaluated by degrading methylene blue (MB) dye under UV-visible light irradiation. The CuO/ZnO with Cu/Zn molar ratio of 4% exhibits the highest photocatalytic activity compared that of the other photocatalysts under the identical conditions. It is mainly attributed to the increased charge separation rate in the nanocomposite and the extended photo-responding range.


2011 ◽  
Vol 364 ◽  
pp. 238-242 ◽  
Author(s):  
Kimi Melody ◽  
Yuliati Leny ◽  
Mustaffa Shamsuddin

A series of In0.1SnxZn0.85-2xS solid solutions was synthesized by hydrothermal method and employed as photocatalyst for photocatalytic hydrogen evolution under visible light irradiation. The structures, optical properties and morphologies of the solid solutions were studied by X-ray diffraction, diffuse reflectance UV–visible spectroscopy and field emission scanning electron microscopy. From the characterizations, it was confirmed that In0.1SnxZn0.85-2xS solid solution can be obtained and they have nanosized particles. The highest photocatalytic activity was observed on In0.1Sn0.03Zn0.79S photocatalyst, with average rate of hydrogen production 3.05 mmol/h, which was 1.2 times higher than the In0.1Zn0.85S photocatalyst.


2019 ◽  
Vol 12 (06) ◽  
pp. 1950085 ◽  
Author(s):  
Di Zhao ◽  
Xuezheng An ◽  
Yaxian Sun ◽  
Guihua Li ◽  
Hongyan Liu ◽  
...  

p-n heterojunction Ag2CO3/Ag3PO4/Ni thin films were prepared by electrochemical co-deposition. The surface morphology and structural properties of the thin films were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS). The photocatalytic (PC) properties of the Ag2CO3/Ag3PO4/Ni composite thin films were investigated by their ability to degrade rhodamine B (RhB) and Congo red (CR) under visible light irradiation. The results showed that the photodegradation efficiency of RhB by an Ag2CO3/Ag3PO4/Ni thin film under visible-light irradiation for 30[Formula: see text]min (98.84%) was 2.64 times higher than that of an Ag3PO4/Ni thin film and 3.44 times higher than of an Ag2CO3/Ni thin film. The presence of a [Formula: see text]-[Formula: see text] heterojunction greatly increased the charge conductivity of the film and its ability to photocatalytically reduce dissolved oxygen, which are the main reasons for the improved PC performance of the Ag2CO3/Ag3PO4/Ni films.


2014 ◽  
Vol 955-959 ◽  
pp. 2267-2275 ◽  
Author(s):  
Rong Liu ◽  
Shi Duo Zhao ◽  
Xue Lin

Ba0.6Mg0.4TiO3 (BMT) particles with different morphologies were synthesized through hydrothermal method and their optical and photocatalytic properties were investigated. Their crystal structure and microstructures were characterized using X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). XRD patterns demonstrate that the as-prepared samples are tetragonal structure. FESEM shows that BMT crystals can be fabricated in different morphologies by simply manipulating the reaction parameters of hydrothermal process. The UV-visible diffuse reflectance spectra (UV-vis DRS) reveal that the band gaps of BMT photocatalysts are about 2.37 - 2.51 eV. The as-prepared BMT photocatalysts exhibite higher photocatalytic activities in the degradation of methyl orange (MO) under visible light irradiation (λ > 420 nm) compared with traditional N-doped TiO2 (N-TiO2) and pure BaTiO3 (BTO). The high photocatalytic performance of BMT photocatalysts could be attributed to the recombination restraint of the e-/h+ pairs resulting from doping of Mg2+ ions. The influence of morphologies upon the photocatalytic properties of BMT was studied. Furthermore, BMT nanowires reveal the highest photocatalytic activity. Up to 94.0% MO is decolorized after visible light irradiation for 360 min.


NANO ◽  
2017 ◽  
Vol 12 (05) ◽  
pp. 1750059 ◽  
Author(s):  
Zhiyuan Yang ◽  
Junjie Wang ◽  
Lu Chen ◽  
Mengjun Liang ◽  
Yulin Xu ◽  
...  

In this work, we developed a simple hydrothermal method toward the fabrication of TiO2/Bi[Formula: see text]Mo[Formula: see text]O[Formula: see text] heterostructure, which had superior photocatalytic performance for degrading of RhB under visible light irradiation. The as-prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), high-resolution transmission electron microscopy (HRTEM), UV-Vis diffuse reflectance spectroscopy (DRS) and photoelectrochemical measurements. The optimal composite with 15[Formula: see text]wt.% TiO2/Bi[Formula: see text]Mo[Formula: see text]O[Formula: see text] (TBMO3) exhibits a much higher photocatalytic activity than that of Bi[Formula: see text]Mo[Formula: see text]O[Formula: see text] and P25 by degradation of RhB under visible light irradiation within 20[Formula: see text]min. The enhanced performance of TBMO3 is predominantly attributed to the synergistic effect both in the higher surface area and the improved separation of photogenerated charge carriers between the two semiconductors. Recycling experiments indicated that TiO2/Bi[Formula: see text]Mo[Formula: see text]O[Formula: see text] photocatalysts had excellent cycle performance and stability. The photocatalytic mechanism of nanocomposite photocatalysts was proposed, which is confirmed by the active species trapping experiments and photoluminescence tests.


2011 ◽  
Vol 183-185 ◽  
pp. 1767-1771
Author(s):  
Gang Xin ◽  
Ju Shen ◽  
Ya Li Meng

The photodegradation of reactive green KE-4BD solution is investigated using N-doped titania (N-TiO2) under visible light irradiation. N-TiO2 is prepared using ammonia or urea as a nitrogen source and characterized by X-ray diffraction, Brunauer-Emmett-Teller methods, and UV-visible diffuse reflectance spectra. The effects of the initial dye concentration and pH on photocatalytic degradation are studied, and the direct correlation between pH, dye concentration, and the rate of degradation are determined. Experimental results show that aqueous solutions of KE-4BD degrade easily in weakly acidic conditions in the presence of N-doped TiO2 (1 g/L) as a photocatalyst. The optimized dye concentration for photolysis is 150 mg/L. The complete degradation of KE-4BD could be achieved under visible light irradiation, and the dye molecules could be partly decomposed into inorganic substances.


2019 ◽  
Vol 23 (04n05) ◽  
pp. 561-568 ◽  
Author(s):  
Gizem Başaran Dindaş ◽  
Zeynel Şahin ◽  
H. Cengiz Yatmaz ◽  
Ümit İşci

CoPc(COOH)[Formula: see text]-TiO[Formula: see text] nanocomposites to be used as efficient visible light photocatalysts were obtained by modifying TiO2 nanoparticles with cobalt(II) tetracarboxyphthalocyanine (CoPc(COOH)[Formula: see text]). The photocatalyst was then characterized by ultra-violet diffuse reflectance spectroscopy (UV-DRS), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). The UV-DRS spectra showed that the absorbance spectrum of the modified catalyst was shifted to the visible region. Different textile dye solutions of Reactive Red 180, Acid Red 88 and Direct Orange 46 were efficiently degraded under visible light. Color removal rates were established to be 30%, 53% and 47% after 180 min for RR180, AR88 and DO46 dyes, respectively. The optimum catalyst concentration was determined to be 1 g/L of CoPc(COOH)[Formula: see text]-TiO[Formula: see text]. Development of the CoPc(COOH)[Formula: see text]-TiO[Formula: see text] nanocomposite photocatalyst enabled the utilization of visible light irradiation for efficient photodegradation of organic textile dye solutions.


2013 ◽  
Vol 864-867 ◽  
pp. 601-604
Author(s):  
Jin Zhang ◽  
Yu Xin Sun

A novel attapulgite clay-based composite (BiVO4/attapulgite) was successfully prepared as a heterogeneous photocatalyst for degradation of rhodamine B (RhB) dye solution under visible light irradiation. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and microanalysis by energy dispersive spectrometry (EDS), and UV-visible diffuse reflectance spectra (DRS). The results showed that monoclinic BiVO4particles were loaded successfully on to the surface of attapulgite fibers and were widely dispersed. The DRS spectrum reveals that the BiVO4/attapulgite composite had much stronger absorption in the visible light range of 420-800 nm. Correspondingly, the BiVO4/attapulgite composite showed significantly higher activity in degrading RhB solution under visible-light irradiation compared to that of pure BiVO4.


2011 ◽  
Vol 383-390 ◽  
pp. 3183-3187 ◽  
Author(s):  
Han Jie Huang ◽  
Wen Long She ◽  
Hai Peng Huang

A visible-light-driven CeVO4/TiO2 photocatalyst with nanostructured heterojunction has been successfully prepared by a simple coupled method. The catalyst was characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS) and spin-trapping electron paramagnetic resonance (EPR). The visible light-induced photocatalytic activities were evaluated by decomposing benzene in gas phase. The result showed that the prepared catalyst exhibited efficient photocatalytic activities with high photochemical stability under visible light irradiation.


2011 ◽  
Vol 335-336 ◽  
pp. 1385-1390 ◽  
Author(s):  
Shuo Wiei Zhao ◽  
Hui Xu ◽  
Hua Ming Li ◽  
Yuan Guo Xu

In order to improve the photocatalytic activity, Co was successfully loaded into Ag3VO4 by using impregnation process. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS) and diffuse reflectance spectroscopy (DRS). The XRD and SEM–EDS analyses revealed that Co ion was dispersed on Ag3VO4. The DRS results indicated that the absorption edge of the Co–Ag3VO4 catalyst shifted to longer wavelength. The enhanced photocatalytic activity of Co–Ag3VO4 for Methylene Blue(MB) dye degradation under visible light irradiation was due to its wider absorption edge and higher separation rate of photo-generated electron and holes. In the experimental conditions, it is demonstrated that the MB was effectively degraded by more than 95% within 40 min when the Co–Ag3VO4 catalyst was calcined at 300°C with 1 wt.% Co content.


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