Preparation and Photocatalytic Properties of Visible-Light-Driven BiVO4/attapulgite Composite

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 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.


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.


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.


2009 ◽  
Vol 79-82 ◽  
pp. 2115-2118
Author(s):  
Xian Hua Zhang ◽  
Lei Ge

The novel visible-light-driven Ag/BiVO4 composite photocatalysts were successfully prepared by photo-deposition method. The as-prepared Ag/BiVO4 samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and UV–vis diffuse reflectance spectra (DRS). The photocatalytic activities of the Ag/BiVO4 powders were determined by degradation of methyl orange molecules in water under visible light irradiation (λ>400nm). The photocatalytic experiments indicated that the composite samples enhanced photo-activity under visible light irradiation.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Pengyu Dong ◽  
Yan Hao ◽  
Peiyang Gao ◽  
Entian Cui ◽  
Qinfang Zhang

Ag3PO4triangular prism was synthesized by a facile chemical precipitation approach by simply adjusting external ultrasonic condition. The as-synthesized Ag3PO4triangular prism was characterized by X-ray diffraction pattern (XRD), field emission scanning electron microscopy (SEM), fourier transform infrared (FTIR) spectra, and ultraviolet-visible diffuse reflectance (UV-vis DRS) absorption spectra. The photocatalytic activity of Ag3PO4triangular prism was evaluated by photodegradation of organic methylene blue (MB), rhodamine B (RhB), and phenol under visible light irradiation. Results showed that Ag3PO4triangular prism exhibited higher photocatalytic activity than N-doped TiO2and commercial TiO2(P25) under visible light irradiation.


2015 ◽  
Vol 2015 ◽  
pp. 1-14 ◽  
Author(s):  
Rong Ran ◽  
Joanne Gamage McEvoy ◽  
Zisheng Zhang

Monoclinic BiVO4powders were synthesized via a novel route using potassium metavanadate (KVO3) prepared by calcination of K2CO3and V2O5as a starting material and followed by hydrothermal treatment and were investigated for the degradation of Rhodamine B (RhB) under visible light irradiation. The synthesized BiVO4particles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV-Visible (UV-Vis) light diffuse reflectance spectrophotometry. The synthesis produced pure monoclinic BiVO4particles with multimorphological features containing flower-like, flake-ball, flake, cuboid-like, and plate-like shapes and exhibited strong absorption in the visible light range. The BiVO4prepared via KVO3possessed excellent photocatalytic activity for the degradation of RhB under visible light. The performance of this catalyst was found to be superior to other BiVO4photocatalysts prepared via ammonium metavanadate (NH4VO3) using coprecipitation, combustion, and calcination methods reported in literature, respectively.


2010 ◽  
Vol 75 (11) ◽  
pp. 1139-1148 ◽  
Author(s):  
Dmitry S. Perekalin ◽  
Evgeniya A. Trifonova ◽  
Ivan V. Glukhov ◽  
Josef Holub ◽  
Alexander R. Kudinov

Reaction of the tricarbollide anion [7,8,9-C3B8H11]– (1a) with the naphthalene complex [CpRu(C10H8)]+ under visible light irradiation in CH2Cl2 gives the 12-vertex closo-ruthenacarborane 1-Cp-1,2,3,5-RuC3B8H11 (2; 87% yield). This complex was also obtained by reaction of 1a with CpRu(cod)Cl (97%). Upon heating at 80 °C in toluene 2 rearranges into isomer 1-Cp-1,2,4,10-RuC3B8H11 (3; 63%). Irradiation of 1a with [CpRu(C10H8)]+ in acetone gives the 11-vertex closo-1-Cp-1,2,3,4-RuC3B7H10 (4; 32%). The latter was also prepared by reaction of 1a with [CpRu(MeCN)3]+ (59%). Compound 2 slowly undergoes cage contraction in acetone giving 4. Irradiation of 1a with [Cp*Ru(C10H8)]+ affords the isomeric 12-vertex closo-ruthenacarboranes 1-Cp*-1,2,3,5-RuC3B8H11 and 1-Cp*-1,2,4,10-RuC3B8H11 (2.2:1 ratio; 56%). Reaction of the amino-substituted tricarbollide anion [7-tBuNH-7,8,9-C3B8H10]– with [(C5R5)Ru(C10H8)]+ (R = H, Me) selectively gives 12-vertex closo-ruthenacarboranes 1-(C5R5)-12-tBuNH-1,2,4,12-RuC3B8H10 (ca. 50%). The structures of 2 and 4 were confirmed by X-ray diffraction.


2021 ◽  
Vol 1035 ◽  
pp. 1043-1049
Author(s):  
Di Xiang ◽  
Chang Long Shao

A simple route has been developed for the synthesis of Ag2O/ZnO heterostructures and the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS) and photoluminescence (PL) spectroscopy analysis. Considering the porous structure of Ag2O/ZnO, the photocatalytic degradation for the organic dyes, such as eosin red (ER), methyl orange (MO), methylene blue (MB) and rhodamine B (RhB), under visible light irradiation was investigated in detail. Noticeably, Ag2O/ZnO just took 40 min to degrade 96 % MB. The rate of degradation using the Ag2O/ZnO heterostructures was 2.3 times faster than that of the bare porous ZnO nanospheres under visible light irradiation due to that the recombination of the photogenerated charge was inhibited greatly in the p-type Ag2O and n-type ZnO semiconductor. So the Ag2O/ZnO heterostuctures showed the potential application on environmental remediation.


2014 ◽  
Vol 636 ◽  
pp. 7-10 ◽  
Author(s):  
Pei Song Tang ◽  
Chao Wan Tang ◽  
Jia Ni Ying ◽  
Dong Jing Ni ◽  
Qian Yang ◽  
...  

Using Fe (NO3)3⋅9H2O, Y(NO3)3⋅6H2O and citric acid as the main raw material, the YFeO3 nanoparticles were synthesized by ultrasonic assisted process and calcination. The YFeO3 nanoparticles were characterized by thermogravimetry and differential thermal analysis (TG-DTA), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-visible diffuse reflectance spectroscopy (DRS). The results show that the perovskite structureYFeO3 (YFeO3-800) can be obtained through the calcination of ultrasonic processed YFeO3 precursors at 800 °C, and the resulting product has a particle size of 70 nm and an optical band gap of 2.0 eV. Consequently, the YFeO3-800 nanoparticles show high photocatalytic activity for decomposition of methyl orange under visible-light irradiation.


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.


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