scholarly journals Tunable Synthesis of Ultrathin BiOCl 2D Nanosheets for Efficient Photocatalytic Degradation of Carbamazepine upon Visible-Light Irradiation

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Shuo Xu ◽  
Xiaoya Gao ◽  
Wenfeng Xu ◽  
Pengfei Jin ◽  
Yongmei Kuang
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Separation Efficiency ◽  
Photogenerated Electron ◽  
Light Irradiation ◽  
Electron Hole ◽  
Magnetic Stirring ◽  
Degradation Activity

A series of ultrathin BiOCl 2D nanosheet photocatalysts were prepared by the TBAOH-assisted hydrolysis method in water. The effects of tetrabutylammonium hydroxide (TBAOH) dosages, chlorine source, preparation pH value, ultrasonic treatment, and magnetic stirring on the photocatalytic degradation dynamics of carbamazepine were examined under visible-light irradiation to optimize the preparation parameters. It was found that ultrathin BiOCl prepared with TBAOH dosages of 1 mmol and chlorine source of NaCl in the pH of 2 upon magnetic stirring of 6 h displayed the highest photocatalytic degradation rate constant (0.0038 min−1) of carbamazepine, which is 7.6 times higher than that with the ordinary BiOCl (without TBAOH). To clarify the mechanism on the outstanding photocatalytic activity of ultrathin BiOCl, the elemental composition/state, micromorphology, and separation efficiency of photogenerated electron-hole pairs were investigated by X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and photoluminescence (PL). Results showed that the presence of oxygen vacancy, ultrathin nanosheet structure, and improved separation efficiency of photogenerated electron-hole pairs contributed to the excellent photocatalytic degradation activity of ultrathin BiOCl. The obtained result provides a novel method to fabricate ultrathin BiOCl with excellent photocatalytic degradation activity of carbamazepine under visible-light irradiation.

Synthesis of g-C3N4/CuS Heterojunction with Enhanced Photocatalytic Activity Under Visible-Light

2020 ◽  
Vol 20 (9) ◽  
pp. 5896-5905
Author(s):  
Fan Wang ◽  
Qingru Zeng ◽  
Jinping Tang ◽  
Liang Peng ◽  
Jihai Shao ◽  
...  
Keyword(s):  
Visible Light ◽  
Visible Light Irradiation ◽  
Separation Efficiency ◽  
Photocatalytic Property ◽  
Photogenerated Electron ◽  
Light Irradiation ◽  
Electron Hole ◽  
Photocatalytic System ◽  
Composite Photocatalysts ◽  
The Stability

Novel g-C3N4/CuS hybrid photocatalysts were synthesized successfully via a facile hydrothermal method. Characterization results of the photocatalysts showed that especial heterostructure had formed between g-C3N4 and CuS, and possess suitable matched band potential. The composite photocatalysts displayed strong UV-visible light absorption ability in the range from 200 to 800 nm. Photocatalytic performance of the photocatalysts were evaluated via photooxidation of methyl orange (MO) under visible-light irradiation. Hybrid photocatalysts showed better photocatalytic properties than that of pure g-C3N4 or CuS. The 60% g-C3N4/CuS sample proved the supreme photocatalytic property. The integrated g-C3N4 and CuS heterojunction elevated the separation efficiency of photogenerated electron–hole pairs, and increased the photo-decoloration efficiency of MO under visible-light irradiation. A four-cycle repeatability experiment was carried out to investigate the stability of hybrid photocatalysts in the photocatalyst reaction. Radical capture experiments proved that photogenerated e−, h+ and .OH were responsible for MO photo-decoloration. In addition, the potential mechanism of the photocatalytic system g-C3N4/CuS+H2O2+vis are presented.

scholarly journals Photocatalytic degradation of deoxynivalenol over dendritic-like α-Fe2O3 under visible light irradiation

Toxins ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 105 ◽  
Author(s):  
Huiting Wang ◽  
Jin Mao ◽  
Zhaowei Zhang ◽  
Qi Zhang ◽  
Liangxiao Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Synthesis Method ◽  
Light Irradiation ◽  
Trichothecene Mycotoxin ◽  
X Ray

Deoxynivalenol (DON) is a secondary metabolite produced by Fusarium, which is a trichothecene mycotoxin. As the main mycotoxin with high toxicity, wheat, barley, corn and their products are susceptible to contamination of DON. Due to the stability of this mycotoxin, traditional methods for DON reduction often require a strong oxidant, high temperature and high pressure with more energy consumption. Therefore, exploring green, efficient and environmentally friendly ways to degrade or reduce DON is a meaningful and challenging issue. Herein, a dendritic-like α-Fe2O3 was successfully prepared using a facile hydrothermal synthesis method at 160 °C, which was systematically characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). It was found that dendritic-like α-Fe2O3 showed superior activity for the photocatalytic degradation of DON in aqueous solution under visible light irradiation (λ > 420 nm) and 90.3% DON (initial concentration of 4.0 μg/mL) could be reduced in 2 h. Most of all, the main possible intermediate products were proposed through high performance liquid chromatography-mass spectrometry (HPLC-MS) after the photocatalytic treatment. This work not only provides a green and promising way to mitigate mycotoxin contamination but also may present useful information for future studies.

Plasmon-Induced Photodegradation of Toxic Pollutants with Ag/AgI/Bi2WO6 under Visible-Light Irradiation

2013 ◽  
Vol 807-809 ◽  
pp. 1534-1542 ◽  
Author(s):  
Ming Sheng Gui ◽  
Peng Fei Wang ◽  
Miao Miao Tang ◽  
Dong Yuan
Keyword(s):  
Surface Plasmon Resonance ◽  
Visible Light ◽  
Surface Plasmon ◽  
Visible Light Irradiation ◽  
Plasmon Resonance ◽  
Photogenerated Electron ◽  
Light Irradiation ◽  
Ag Nps ◽  
Electron Hole ◽  
Band Position

The Ag/AgI/Bi2WO6photocatalysts were successfully synthesized by deposition-precipitation and photoreduction methods. The catalyst showed high and stable photocatalytic activity for the degradation of the RhB under visible light irradiation (λ>400 nm). On the basis of a new plasmonic photocatalytic mechanism, the photogenerated electron-hole pairs are formed in Ag nanoparticles (NPs) due to surface plasmon resonance under visible-light irradiation. Then, the photoexcited electrons at the Ag NPs are injected into AgI. On the other hand, the band position shows that AgI and Bi2WO6have the matching band potentials in the AgI/Bi2WO6heterostructure composites. So the photoexcited electrons is ultimately transfer to the Bi2WO6conduction band (CB), photo-induced holes (hVB+) is transfer to the AgI valence band (VB) and the simultaneous transfer to compensative electrons from I-to the Ag NPS. This the result indicates that the high photosensitivity of noble metal Ag NPs due to surface plasmon resonance, which is not only improve the photocatalytic performance, but also offer a new idea for preparation of new photocatalysts .

scholarly journals Enhanced Activation of Persulfate by Co-Doped Bismuth Ferrite Nanocomposites for Degradation of Levofloxacin Under Visible Light Irradiation

Materials ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 3952 ◽  
Author(s):  
Xin Zhong ◽  
Zheng-Shuo Zou ◽  
Hu-Lin Wang ◽  
Wei Huang ◽  
Bin-Xue Zhou
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Degradation Mechanism ◽  
Bismuth Ferrite ◽  
Light Condition ◽  
Photogenerated Electron ◽  
Active Species ◽  
Light Irradiation ◽  
Co Doped

In this study, magnetic visible light driven photocatalysts (bismuth ferrite, Bi2Fe4O9, BFO and Co-doped bismuth ferrite, Co-BFO) were successfully prepared by the facile hydrothermal method. The catalyst was used in the application of heterogeneous persulfate (PS) system under visible LED light irradiation for the degradation of levofloxacin (LFX), proving to be an excellent photocatalyst when evaluated by various characterization methods. The effect of Co-doping in the BFO structure was investigated that the decrease of band gap width and the generated photoelectrons and holes would effectively reduce the recombination of photogenerated electron-hole pairs, leading to the enhancement photocatalytic activity. The results demonstrated that Co-BFO catalyst had a high photodegradation efficiency over a wide pH range of 3.0–9.0 and the Co-BFO-2 composite displayed the optimal catalytic performance. It was found that the degradation rate of LFX by Co-BFO-2 catalyst was 3.52 times higher than that of pure BFO catalyst under visible light condition. The free radical trapping experiments and EPR tests demonstrated that superoxide, photogenerated holes and sulfate radicals were the main active species in the photocatalytic degradation of LFX. And a possible photocatalytic degradation mechanism of LFX was proposed in the Vis/Co-BFO/PS process. These findings provided new insight of the mechanism of heterogeneous activation of persulfate by Co-BFO under visible light irradiation.

pH-Controlled photocatalytic abatement of RhB by an FeWO4/BiPO4 p–n heterojunction under visible light irradiation

2019 ◽  
Vol 43 (44) ◽  
pp. 17241-17250
Author(s):  
Nithya Mahendran ◽  
Sathya Udayakumar ◽  
Keerthi Praveen
Keyword(s):  
Electric Field ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Separation Efficiency ◽  
Light Irradiation ◽  
The Novel ◽  
Electron Hole ◽  
Ph Controlled

The novel FeWO4/BiPO4 heterojunction generates an inner electric field to promote electron–hole separation efficiency and is a proficient photocatalyst.

Preparation of BiXY(2-X)O3 and its Photocatalytic Degradation of Molasses Fermentation Wastewater under Visible-Light Irradiation

2011 ◽  
Vol 287-290 ◽  
pp. 1640-1645 ◽  
Author(s):  
Min Guang Fan ◽  
Zu Zeng Qin ◽  
Zi Li Liu ◽  
Tong Ming Su
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Diffuse Reflectance Spectroscopy ◽  
Active Oxygen Species ◽  
Light Irradiation ◽  
X Ray

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.

A simple method to synthesise Ag-doped TiO2 photocatalysts with different Ag0:Ag2O atomic ratios for enhancing visible-light photocatalytic activity

2017 ◽  
Vol 41 (8) ◽  
pp. 475-483 ◽  
Author(s):  
C. Chen ◽  
X. F. Lei ◽  
M. Z. Xue
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Absorption ◽  
Separation Efficiency ◽  
Visible Region ◽  
Light Irradiation ◽  
Electron Hole ◽  
X Ray

Pure anatase TiO2 photocatalysts with different Ag contents were prepared via a simple sol-gel method. The as-prepared anatase Ag-doped TiO2 photocatalysts were characterised by X-ray diffraction, transmission electron microscopy, UV-Vis diffuse reflectance spectra, photoluminescence spectroscopy, X-ray photoelectron spectroscopy, thermal gravity and differential thermal analysis, scanning electron microscopy and N2 adsorption–desorption measurements (BET). Compared with pure TiO2, Ag-doped anatase TiO2 photocatalysts exhibited not only increases in light absorption in the visible region, the separation efficiency of electron–hole pairs and surface area, but also inhibition of the titania phase transition from anatase to rutile. Photoreduction results showed that Ag-doped anatase TiO2 photocatalysts have greatly improved photocatalytic activity, compared with pure TiO2, and the reduction of Cr(VI) under visible light irradiation was much higher than that of pure TiO2. The optimum Ag content was 1.0 mol%, which led to the complete reduction of Cr(VI) under visible light irradiation (λ > 420 nm) for 4 h. The enhanced photocatalytic activity was attributed to the synergic effect of the pure anatase structure, and the increased light absorption in the visible region, separation efficiency of electron–hole pairs and atomic ratio of Ag0:Ag2O.

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