scholarly journals One-Pot Synthesized Visible Light-Driven BiOCl/AgCl/BiVO4 n-p Heterojunction for Photocatalytic Degradation of Pharmaceutical Pollutants

Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2297 ◽  
Author(s):  
Rokhsareh Akbarzadeh ◽  
Anvar Asadi ◽  
Peter Ozaveshe Oviroh ◽  
Tien-Chien Jen

A novel enhanced visible light absorption BiOCl/AgCl/BiVO4 heterojunction of photocatalysts could be obtained through a one-pot hydrothermal method used with two different pH solutions. There was a relationship between synthesis pH and the ratio of BiOCl to BiVO4 in XRD planes and their photocatalytic activity. The visible light photocatalytic performances of photocatalysts were evaluated via degradation of diclofenac (DCFF) as a pharmaceutical model pollutant. Furthermore, kinetic studies showed that DCF degradation followed pseudo-first-order kinetics. The photocatalytic degradation rates of BiOCl/AgCl/BiVO4 synthesized at pH = 1.2 and pH = 4 for DCF were 72% and 47%, respectively, showing the higher activity of the photocatalyst which was synthesized at a lower pH value. It was concluded that the excellent photocatalytic activity of BiOCl/AgCl/BiVO4 is due to the enhanced visible light absorption formation of a heterostructure, which increased the lifetime of photo-produced electron–hole pairs by creating a heterojunction. The influence of pH during synthesis on photocatalytic activity in order to create different phases was investigated. This work suggests that the BiOCl/AgCl/BiVO4 p-n heterojunction is more active when the ratio of BiOCl to BiVO4 is smaller, and this could be achieved simply by the pH adjustment. This is a promising method of modifying the photocatalyst for the purpose of pollutant degradation under visible light illumination.

RSC Advances ◽  
2016 ◽  
Vol 6 (96) ◽  
pp. 93887-93893 ◽  
Author(s):  
Feng Guo ◽  
Weilong Shi ◽  
Yi Cai ◽  
Shuwen Shao ◽  
Tao Zhang ◽  
...  

Sheet-on-sphere Ag/AgBr@InVO4 displayed excellent photocatalytic degradation of RhB, which was attributed to enhanced visible-light absorption and anti-combination of electrons/holes through it's heterostructure.


Author(s):  
David Maria Tobaldi ◽  
Luc Lajaunie ◽  
ana caetano ◽  
nejc rozman ◽  
Maria Paula Seabra ◽  
...  

<div>Titanium dioxide is by far the most utilised semiconductor material for photocatalytic applications. Still, it is transparent to visible-light. Recently, it has been proved that a type-II band alignment for the rutile−anatase mixture would improve its visible-light absorption.</div><div>In this research paper we thoroughly characterised the real crystalline and amorphous phases of synthesised titanias – thermally treated at different temperatures to get distinct ratios of anatase-rutile-amorphous fraction – as well as that of three commercially available photocatalytic nano-TiO2. </div><div>The structural characterisation was done via advanced X-ray diffraction method, namely the Rietveld-RIR method, to attain a full quantitative phase analysis of the specimens. The microstructure was also investigated via an advanced X-ray method, the whole powder pattern modelling. These methods were validated combining advanced aberration-corrected scanning transmission microscopy and high-resolution electron energy-loss spectroscopy. The photocatalytic activity was assessed in the liquid- and gas-solid phase (employing rhodamine B and 4-chlorophenol, and isopropanol, respectively, as the organic substances to degrade) using a light source irradiating exclusively in the visible-range.</div><div>Optical spectroscopy showed that even a small fraction of rutile (2 wt%) is able to shift to lower energies the apparent optical band gap of an anatase-rutile mixed phase. But is this enough to attain a real photocatalytic activity promoted by merely visible-light?</div><div>We tried to give a reply to that question.</div><div>Photocatalytic activity results in the liquid-solid phase showed that a high surface hydroxylation led to specimen with superior visible light-induced catalytic activity (i.e. dye and ligand-to-metal charge transfer complexes sensitisation effects). That is: not photocatalysis <i>sensu-strictu</i>.</div><div>On the other hand, the gas-solid phase results showed that a higher amount of the rutile fraction (around 10 wt%), together with less recombination of the charge carriers, were more effective for an actual photocatalytic oxidation of isopropanol.</div>


Author(s):  
Mehala Kunnamareddy ◽  
Ranjith Rajendran ◽  
Megala Sivagnanam ◽  
Ramesh Rajendran ◽  
Barathi Diravidamani

AbstractIn this work, Nickel (Ni) and sulfur (S) codoped TiO2 nanoparticles were prepared by a sol-gel technique. The as-prepared catalyst was characterized using X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), FT-Raman spectroscopy, scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectra (DRS) for investigating crystal structure, crystal phase, particle size and bandgap energy of these samples. The photocatalytic performances of all the prepared catalysts have been investigated for the degradation of methylene blue (MB) under visible light irradiation. It was noticed that Ni-S codoped TiO2(Ni-S/TiO2) nanoparticles exhibited much higher photocatalytic activity compared with pure, Ni and S doped TiO2 due to higher visible light absorption and probable decrease in the recombination of photo-generated charges. It was decided that the great visible light absorption was created for codoped TiO2 by the formation of impurity energy states near both the edges of the collection, which works as trapping sites for both the photogenerated charges to decrease the recombination process.


2015 ◽  
Vol 1806 ◽  
pp. 19-24 ◽  
Author(s):  
John E. Mathis

ABSTRACTThere is great interest in improving TiO2’s photocatalytic activity in the visible portion of electromagnetic spectrum. Recent work has shown that co-doping mesoporous TiO2 microparticles with a transition metal and nitrogen, hereby designated as (M,N) TiO2, significantly increases its visible light absorption. However, the hydrothermal method used to produce the microparticles creates a wide distribution in the size of the microparticles, which could affect the absorption properties. Recently, it has become possible to produce monodisperse, mesoporous TiO2 microparticles with engineered sizes using a hybrid sol-gel/hydrothermal technique. Further, it has also been shown that the size of monodisperse TiO2 microparticles affects the the photocatalytic activity.This study investigated whether using mondodisperse (M,N) TiO2 microparticles would further increase visible-light absorption for (M,N)TiO2. The first-row transition metals chosen for this study - Mn, Fe, Co, Ni, and Cu – have been characterized in the earlier (M,N) TiO2 UV-vis study, which was used as a baseline. The doping levels of the transition metals samples were set at the 2.5 percent level previously shown to be optimum for photocatalytic activity.


2020 ◽  
Vol 7 (12) ◽  
pp. 2343-2351
Author(s):  
Ran Wang ◽  
Guoan Lin ◽  
Xiaoxiang Xu

La/Zr co-doping preserves visible light absorption of SrTaO2N, prohibits the formation of defects, improves surface hydrophilicity and charge separation conditions, all of which contribute to an enhanced photocatalytic activity for water reduction.


2020 ◽  
pp. 174751982093867
Author(s):  
Zhen Zhang ◽  
Shao-dong Qin ◽  
Jing-yun Chen ◽  
Jing Li ◽  
Ai-hua Xing

The synthesis of surface defect TiO2-x nanobelts with excellent visible light absorption is important to reduce costs, increase stability, and improve photocatalytic activity. In this work, we report that nitrogen-doped surface defect TiO2-x nanobelts are synthesized by annealing pristine TiO2 nanobelts in Ar/H2 (95%/5%) atmosphere followed by subsequent heat treatment in NH3 at various temperatures. The aim is to study the effect of the extent of the N-doping amount in the lattice of TiO2-x nanobelts on light absorption and photocatalytic activity. Considering the increase in organic pollutants in wastewater, the photocatalytic activity is measured by degrading rhodamine B (RhB) dye in water. The results demonstrate that the calcination temperature affects the doping level of N, and the b-TiO2-N550 sample exhibits higher photocatalytic performance than that of other samples under visible-light irradiation for the degradation of rhodamine B, which is up to 96.11%. The enhancement is ascribed to the synergistic effect of N-doping and self-doping oxygen vacancy (which extend the visible light absorption) and the separation efficiency of photogenerated carriers, which improves the photocatalytic activity.


RSC Advances ◽  
2015 ◽  
Vol 5 (35) ◽  
pp. 27690-27698 ◽  
Author(s):  
Ahmad S. Alshammari ◽  
Lina Chi ◽  
Xiaoping Chen ◽  
Abdulaziz Bagabas ◽  
Denis Kramer ◽  
...  

Heavy C-doping can effectively enhance visible-light absorption yet exhibited lower visible-light-responsive photocatalytic activity due to significant recombination of photogenerated charge carriers caused by C-dopant and oxygen vacancies.


RSC Advances ◽  
2016 ◽  
Vol 6 (72) ◽  
pp. 68530-68537 ◽  
Author(s):  
Yun Liu ◽  
Yu-jie Ma ◽  
Chun-yan Liu ◽  
Zhi-ying Zhang ◽  
Wen-dong Yang ◽  
...  

A carbon dot–silica hybrid with a high dosage of CDs demonstrated significant visible light absorption, a large Cr(vi) adsorption capacity and good photocatalytic activity for the reduction of Cr(vi) in visible light.


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