scholarly journals Preparation and Characterization of Highly Efficient and Stable Visible-Light-Responsive Photocatalyst AgBr/Ag3PO4

2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
Zhang Jinfeng ◽  
Zhang Tao

AgBr/Ag3PO4photocatalyst was synthesized using a facile coprecipitation method. The photocatalyst was characterized by X-ray powder diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) surface areas, and photoluminescence (PL) technique. The activity of the photocatalyst was evaluated by the degradation of methyl orange (MO) and rhodamine B (RhB). The results showed that the prepared AgBr/Ag3PO4exhibited excellent performance and much higher photocatalytic activity than the single one under visible-light irradiation. The optimum mole ratio of Br/P in AgBr/Ag3PO4samples is 0.3. The prepared AgBr/Ag3PO4photocatalyst was transformed to Ag/AgBr/Ag3PO4system with excellent property and good stability in the photocatalytic process. The possible mechanisms of the enhanced photocatalytic activity for the AgBr/Ag3PO4were also discussed in detail.

2015 ◽  
Vol 2015 ◽  
pp. 1-6
Author(s):  
Liqin Qin ◽  
Pingfang Tao ◽  
Xiaosong Zhou ◽  
Qi Pang ◽  
Chunjie Liang ◽  
...  

A facile method for the synthesis of Ag3PO4visible light photocatalyst has been developed to improve the photocatalytic activity and stability. The as-prepared samples are investigated by X-ray powder diffraction, scanning electron microscopy, infrared spectroscopy, photoluminescence (PL) spectroscopy, and UV-Vis diffuse reflectance spectroscopy techniques. The results reveal that the prepared Ag3PO4has cube structure with a band gap of 2.26 eV. The as-prepared samples show higher photocatalytic activity for methylene blue (MB) degradation than that of N-TiO2under visible light irradiation.


2014 ◽  
Vol 809-810 ◽  
pp. 890-894
Author(s):  
Dan Li ◽  
Lian Wei Shan ◽  
Gui Lin Wang ◽  
Li Min Dong ◽  
Wei Li ◽  
...  

Boron-BiVO4 samples were synthesized by sol-gel method. They were characterized by UV-vis diffuse reflectance spectroscopy, X-ray diffraction. Photocatalytic activity of the obtained BiVO4 samples was investigated through degrading methylene blue (MB). The results reveal that boron-BiVO4 catalysts have monoclinic scheelite structure. The BiVO4 and Co-BiVO4 photocatalysts were responsive to visible light. Co-BiVO4 photocatalyst showed higher photocatalytic activity than pure BiVO4, resulting in the significantly improved efficiency of degradation of MB.


2011 ◽  
Vol 287-290 ◽  
pp. 1640-1645 ◽  
Author(s):  
Min Guang Fan ◽  
Zu Zeng Qin ◽  
Zi Li Liu ◽  
Tong Ming Su

A series of BixY(2-x)O3photocatalysts were successfully prepared by a solid-state reaction and were subsequently characterized by powder X-ray diffraction, UV-vis diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy (XPS). The UV-vis diffuse reflectance spectra revealed that the BixY(2-x)O3samples absorbed light in the visible-light range (400-800 nm). The XPS results indicated that active oxygen species were generated on the Bi1.8Y0.2O3surface, which displayed a higher photocatalytic activity. When using photocatalytic degradation molasses fermentation wastewater as a model reaction, the Bi1.8Y0.2O3showed higher photocatalytic activity in comparison to Bi0.2Y1.8O3under visible-light irradiation.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Yunling Zou ◽  
Xianshou Huang ◽  
Tao Yu ◽  
Xiaoqiang Tong ◽  
Yan Li ◽  
...  

Abstract Cu-doped TiO2 having a brookite phase and showing enhanced visible light photocatalytic activity was synthesized using a mild solvothermal method. The as-prepared samples were characterized by various techniques, such as X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy. Photocatalytic activity of Cu-doped brookite TiO2 nanoparticles was evaluated by photodegradation of methylene blue under visible light irradiation. The X-ray diffraction analysis showed that the crystallite size of Cu-doped brookite TiO2 samples decreased with the increase of Cu concentration in the samples. The UV-Vis diffuse reflectance spectroscopy analysis of the Cu-doped TiO2 samples showed a shift to lower energy levels in the band gap compared with that of bare phase brookite TiO2. Cu doped brookite TiO2 can obviously improve its visible light photocatalytic activity because of Cu ions acting as electron acceptors and inhibiting electron-hole recombination. The brookite TiO2 sample with 7.0 wt.% Cu showed the highest photocatalytic activity and the corresponding degradation rate of MB (10 mg/L) reached to 87 % after visible light illumination for 120 min, much higher than that of bare brookite TiO2 prepared under the same conditions (78 %).


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Quan Gu ◽  
Huaqiang Zhuang ◽  
Jinlin Long ◽  
Xiaohan An ◽  
Huan Lin ◽  
...  

The C-doped CdO photocatalysts were simply prepared by high-temperature solid-state process. The as-prepared photocatalysts were characterized by X-ray powder diffraction (XRD), diffuse reflectance spectroscopy (UV-Vis DRS), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The results demonstrated that the carbon was doped into CdO, resulting in the red-shift of the optical absorption of CdO. The photocatalytic behavior of CdO and C-doped CdO was evaluated under the visible light irradiation by using the photocatalytic hydrogen evolution as a model reaction. The C-doped CdO photocatalysts had higher photocatalytic activity over parent CdO under visible light irradiation. The results indicated that the H2production was due to the existence of CdS and the enhancement of visible light photocatalytic activity of H2production was originated from the doping of carbon into the CdO lattice. The probably reaction mechanism was also discussed and proposed.


2011 ◽  
Vol 391-392 ◽  
pp. 1117-1122 ◽  
Author(s):  
Qi Xiao ◽  
Chi Yao

The C, N, S-tridoped TiO2nanosheets are synthesized via hydrothermal synthesis and post-treatment, and characterized by X-ray diffraction (XRD), Transmission electron microscopy (TEM), X-ray photoelectron spectra (XPS), and UV–vis diffuse reflectance spectroscopy. The UV-diffuse reflectance spectra of all the C, N, S-tridoped TiO2nanosheets greatly extends the absorption edge into the visible light region, which can be attributed to C, N, S-tridoping in the form of cation C-doping, interstitial N-doping, anionic S-doping, and adsorbed SO42-ions states. The C, N, S-tridoped TiO2nanosheets exhibits high visible light photocatalytic activity, and the xanthate concentration reduce as much as 100% in 120 min. All these indicate that C, N, S-tridoped TiO2nanosheets photocatalysts are promising visible light photocatalyst for the practical application.


2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Jin-Hua Cai ◽  
Jin-Wang Huang ◽  
Han-Cheng Yu ◽  
Liang-Nian Ji

In order to utilize visible light more efficiently in the photocatalytic reaction, microspheres sensitized by 5-(4-allyloxy)phenyl-10,15,20-tri(4-methylphenyl)porphyrin (APTMPP) were prepared and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), nitrogen physisorption, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR) and UV-vis diffuse reflectance spectroscopy, and so forth, The characterization results indicated that APTMPP-MPS- was composed of the anatase crystal phase. The morphology of the composite materials was spheriform with size of 0.3–0.7 μm and the porphyrin was chemisorbed on the surface of through a Si–O–Ti bond. The photooxidation ofα-terpinene was employed as the model reaction to evaluate the photocatalytic activity of APTMPP-MPS- microspheres under visible light. The results indicated that the photodegradation ofα-terpinene was significantly enhanced in the presence of the APTMPP-MPS- compared with the nonmodified under visible light.


2014 ◽  
Vol 809-810 ◽  
pp. 140-143 ◽  
Author(s):  
Chao Wan Tang ◽  
Jia Ni Ying ◽  
Dong Jing Ni ◽  
Qian Yang ◽  
Li Mei Wu ◽  
...  

Using Er (NO3)3·5H2O and Fe (NO3)3·9H2O as major materials, the ErFeO3 nanoparticles were prepared by successive microwave processing and high temperature calcination. The samples were characterized by thermogravimetric and differential thermal analysis (TG-DTA), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-visible diffuse reflectance spectroscopy (DRS). It was found that the single phase ErFeO3 can be obtained through the calcination of microwave processed ErFeO3 precursors at 800°C, and the resulting product was approximation flake of 20-80 nm. The visible-light photocatalytic activity of ErFeO3 nanoparticles was investigated in experimental simulation wastewater containing 10 mg/L methyl orange (MO). The results show that ErFeO3 nanoparticles appear high photocatalytic activity for the decomposition of MO 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.


2018 ◽  
Vol 32 (17) ◽  
pp. 1850185 ◽  
Author(s):  
Yun-Hui Si ◽  
Yu Xia ◽  
Ya-Yun Li ◽  
Shao-Ke Shang ◽  
Xin-Bo Xiong ◽  
...  

A series of BiFeO3 and BiFe[Formula: see text]Mn[Formula: see text]O3 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.10) were synthesized by a hydrothermal method. The samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy (EDS) and UV–Vis diffuse reflectance spectroscopy, and their photocatalytic activity was studied by photocatalytic degradation of methylene blue in aqueous solution under visible light irradiation. The band gap of BiFeO3 was significantly decreased from 2.26 eV to 1.90 eV with the doping of Mn. Furthermore, the 6% Mn-doped BiFeO3 photocatalyst exhibited the best activity with a degradation rate of 94% after irradiation for 100 min. The enhanced photocatalytic activity with Mn doping could be attributed to the enhanced optical absorption, increment of surface reactive sites and reduction of electron–hole recombination. Our results may be conducive to design more efficient photocatalysts responsive to visible light among narrow band gap semiconductors.


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