scholarly journals Synergistic Effect on Photocatalytic Activity of Co-Doped NiTiO3/g-C3N4 Composites under Visible Light Irradiation

Catalysts ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1332
Author(s):  
Duc Quang Dao ◽  
Thi Kim Anh Nguyen ◽  
Thanh-Truc Pham ◽  
Eun Woo Shin

Co-doped NiTiO3/g-C3N4 composite photocatalysts were prepared by a modified Pechini method to improve their photocatalytic activity toward methylene blue photodegradation under visible light irradiation. The combination of Co-doped NiTiO3 and g-C3N4 and Co-doping into the NiTiO3 lattice synergistically enhanced the photocatalytic performance of the composite photocatalysts. X-ray photoelectron spectroscopy results for the Co-doped NiTiO3/g-C3N4 composite photocatalysts confirmed Ti-N linkages between the Co-doped NiTiO3 and g-C3N4. In addition, characteristic X-ray diffraction peaks for the NiTiO3 lattice structure clearly indicated substitution of Co into the NiTiO3 lattice structure. The composite structure and Co-doping of the C-x composite photocatalysts (x wt % Co-doped NiTiO3/g-C3N4) not only decreased the emission intensity of the photoluminescence spectra but also the semicircle radius of the Nyquist plot in electrochemical impedance spectroscopy, giving the highest kapp value (7.15 × 10−3 min−1) for the C-1 composite photocatalyst.

2011 ◽  
Vol 179-180 ◽  
pp. 192-196
Author(s):  
Ye Cong ◽  
Peng Qin ◽  
Xuan Ke Li ◽  
Zhi Jun Dong ◽  
Guan Ming Yuan

Nitrogen and lanthanum co-doped nanocsystalline titania photocatalysts were prepared by a homogeneous precipitation-hydrothermal process. The photocatalytic activity of the prepared samples on photodegradation of rhodamine B in visible light irradiation was studied. The nitrogen and lanthanum co-doping could greatly improve the photocatalytic activity of titania in visible light irradiation, probablely due to a synergistic effect of co-doping. The nitrogen doping could narrow the band gap of titania and enhance the utilization efficiency of visible light, while the lanthanum doping could accelerate the separation of photo-generated electrons and holes. Furthermore, the lanthanum doping could increase the adsorption of organic pollutants on the surface of photocatalyst.


NANO ◽  
2016 ◽  
Vol 11 (09) ◽  
pp. 1650105 ◽  
Author(s):  
Xiaoting Meng ◽  
Xiaofang Cheng ◽  
Dongrong Zhuang ◽  
Shaogui Yang ◽  
Cheng Sun

A series of Ag3PO4/BiOCOOH composite photocatalysts have been successfully synthesized by a simple in situ ion precipitation method. The crystallinity, morphology, microstructure, composition and optical property were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), energy dispersive spectrum (EDS), Fourier transform infrared spectrometer (FT-IR), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectrophotometer (DRS). The as-prepared catalysts exhibited excellent photocatalytic activity for the degradation of RhB and MB under visible light irradiation, the 2:1 Ag3PO4/BiOCOOH exhibited the best photocatalytic activity. By adding different free radical scavengers, the catalytic mechanism was discussed. In the process of degradation of RhB, holes (h[Formula: see text] is the main active species, [Formula: see text]O[Formula: see text] played a certain active role, [Formula: see text]OH played a small role. In the process of degradation MB, holes (h[Formula: see text] is the main active species too, [Formula: see text]O[Formula: see text] also played a certain active role, [Formula: see text]OH almost does not work.


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.


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.


2020 ◽  
Vol 35 (3) ◽  
pp. 312-320
Author(s):  
Zuowei Zhang ◽  
Hongshun Hao ◽  
Shanshan Jin ◽  
Yunxia Hou ◽  
Hongman Hou ◽  
...  

Abstract


2020 ◽  
Vol 46 (15) ◽  
pp. 24744-24752 ◽  
Author(s):  
Weichao Li ◽  
Linkun Xie ◽  
Liexing Zhou ◽  
Josias Ochoa-Lozano ◽  
Chen Li ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 342 ◽  
Author(s):  
Mohammed Ismael ◽  
Michael Wark

Perovskite-type oxides lanthanum ferrite (LaFeO3) photocatalysts were successfully prepared by a facile and cost-effective sol-gel method using La(NO)3 and Fe(NO)3 as metal ion precursors and citric acid as a complexing agent at different calcination temperatures. The properties of the resulting LaFeO3 samples were characterized by powder X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDXS), UV-Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectra (IR), transmission electron microscopy (TEM), N2 adsorption/desorption and photoelectrochemical tests. The photoactivity of the LaFeO3 samples was tested by monitoring the photocatalytic degradation of Rhodamine B (RhB) and 4-chlorophenol (4-CP) under visible light irradiation, the highest photocatalytic activity was found for LaFeO3 calcined at 700 °C, which attributed to the relatively highest surface area (10.6 m2/g). In addition, it was found from trapping experiments that the reactive species for degradation were superoxide radical ions (O2−) and holes (h+). Photocurrent measurements and electrochemical impedance spectroscopy (EIS) proved the higher photo-induced charge carrier transfer and separation efficiency of the LaFeO3 sample calcined at 700 °C compared to that that calcined at 900 °C. Band positions of LaFeO3 were estimated using the Mott-Schottky plots, which showed that H2 evolution was not likely.


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