scholarly journals Preparation of a g-C3N4/UiO-66-NH2/CdS Photocatalyst with Enhanced Visible Light Photocatalytic Activity for Tetracycline Degradation

Nanomaterials ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1824 ◽  
Author(s):  
Hao Zhang ◽  
Jialiang Li ◽  
Xianglei He ◽  
Bo Liu

A combination of calcination and hydrothermal processing was used to prepare a g-C3N4/UiO-66-NH2/CdS photocatalyst, and the degradation of tetracycline (TC) over this material was assessed. The photocatalytic performance of this nanocomposite was approximately 4.4 and 2.3 times those of CdS and g-C3N4, respectively, and was found to be affected by the CdS loading amount, the pH of the reaction solution and the initial TC concentration. This catalyst also exhibited stable performance over four consecutive reaction cycles. The highly enhanced photoactivity of the g-C3N4/UiO-66-NH2/CdS is attributed to the introduction of CdS, which widens the range over which the material absorbs visible light and inhibits the recombination of electron–hole pairs. The results of this study suggest further applications for this material in the treatment of contaminated wastewater powered by solar energy.

2020 ◽  
Vol 10 (9) ◽  
pp. 3238
Author(s):  
Min Liu ◽  
Guangxin Wang ◽  
Panpan Xu ◽  
Yanfeng Zhu ◽  
Wuhui Li

In this study, the Ag3PO4/SnO2 heterojunction on carbon cloth (Ag3PO4/SnO2/CC) was successfully fabricated via a facile two-step process. The results showed that the Ag3PO4/SnO2/CC heterojunction exhibited a remarkable photocatalytic performance for the degradation of Rhodamine B (RhB) and methylene blue (MB), under visible light irradiation. The calculated k values for the degradation of RhB and MB over Ag3PO4/SnO2/CC are 0.04716 min−1 and 0.04916 min−1, which are higher than those calculated for the reactions over Ag3PO4/SnO2, Ag3PO4/CC and SnO2/CC, respectively. The enhanced photocatalytic activity could mainly be attributed to the improved separation efficiency of photogenerated electron-hole pairs, after the formation of the Ag3PO4/SnO2/CC heterojunction. Moreover, carbon cloth with a large specific surface area and excellent conductivity was used as the substrate, which helped to increase the contact area of dye solution with photocatalysts and the rapid transfer of photogenerated electrons. Notably, when compared with the powder catalyst, the catalysts supported on carbon cloth are easier to quickly recycle from the pollutant solution, thereby reducing the probability of recontamination.


Materials ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 3948
Author(s):  
Lingfang Qiu ◽  
Zhiwei Zhou ◽  
Mengfan Ma ◽  
Ping Li ◽  
Jinyong Lu ◽  
...  

Novel visible-light responded aluminosilicophosphate-5 (SAPO-5)/g-C3N4 composite has been easily constructed by thermal polymerization for the mixture of SAPO-5, NH4Cl, and dicyandiamide. The photocatalytic activity of SAPO-5/g-C3N4 is evaluated by degrading RhB (30 mg/L) under visible light illumination (λ > 420 nm). The effects of SAPO-5 incorporation proportion and initial RhB concentration on the photocatalytic performance have been discussed in detail. The optimized SAPO-5/g-C3N4 composite shows promising degradation efficiency which is 40.6% higher than that of pure g-C3N4. The degradation rate improves from 0.007 min−1 to 0.022 min−1, which is a comparable photocatalytic performance compared with other g-C3N4-based heterojunctions for dye degradation. The migration of photo-induced electrons from g-C3N4 to the Al site of SAPO-5 should promote the photo-induced electron-hole pairs separation rate of g-C3N4 efficiently. Furthermore, the redox reactions for RhB degradation occur on the photo-induced holes in the g-C3N4 and Al sites in SAPO-5, respectively. This achievement not only improves the photocatalytic activity of g-C3N4 efficiently, but also broadens the application of SAPOs in the photocatalytic field.


Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2206
Author(s):  
Gaoqian Yuan ◽  
Gen Zhang ◽  
Kezhuo Li ◽  
Faliang Li ◽  
Yunbo Cao ◽  
...  

Loading a noble metal on Bi4Ti3O12 could enable the formation of the Schottky barrier at the interface between the former and the latter, which causes electrons to be trapped and inhibits the recombination of photoelectrons and photoholes. In this paper, AgPt/Bi4Ti3O12 composite photocatalysts were prepared using the photoreduction method, and the effects of the type and content of noble metal on the photocatalytic performance of the catalysts were investigated. The photocatalytic degradation of rhodamine B (RhB) showed that the loading of AgPt bimetallic nanoparticles significantly improved the catalytic performance of Bi4Ti3O12. When 0.10 wt% noble metal was loaded, the degradation rate for RhB of Ag0.7Pt0.3/Bi4Ti3O12 was 0.027 min−1, which was respectively about 2, 1.7 and 3.7 times as that of Ag/Bi4Ti3O12, Pt/Bi3Ti4O12 and Bi4Ti3O12. The reasons may be attributed as follows: (i) the utilization of visible light was enhanced due to the surface plasmon resonance effect of Ag and Pt in the visible region; (ii) Ag nanoparticles mainly acted as electron acceptors to restrain the recombination of photogenerated electron-hole pairs under visible light irradiation; and (iii) Pt nanoparticles acted as electron cocatalysts to further suppress the recombination of photogenerated electron-hole pairs. The photocatalytic performance of Ag0.7Pt0.3/Bi4Ti3O12 was superior to that of Ag/Bi4Ti3O12 and Pt/Bi3Ti4O12 owing to the synergistic effect between Ag and Pt nanoparticles.


2018 ◽  
Vol 281 ◽  
pp. 848-853
Author(s):  
Ling Fang Qiu ◽  
Xiao Bin Qiu ◽  
Zhi Wei Zhou ◽  
Shu Wang Duo

Graphitic carbon nitride is a promising photocatalyst for environmental purification, but the photocatalytic performance is limited significantly due to its narrow visible-light adsorption and high photo-reduced electron-hole recombination rate. This work developed a novel way to overcome the two defects and obtained obvious effect. CoAPO-5 was used to broaden visible-light adsorption range by conducting g-C3N4/CoAPO-5 binary composite. In further, rGO was integrated into the binary system to form novel ternary composite. rGO performs as a electron mediator, which can inhibit photo-reduced electron-hole recombination efficiently. The samples were characterized by XRD, SEM, PL, IR and DRS. The photocatalytic performances for degrading RhB (10mg/L) indicated that g-C3N4/CoAPO-5/rGO have much higher activity than g-C3N4/CoAPO-5 because of synergistic effect. When the doping content of rGO in g-C3N4/CoAPO-5 was 0.5%, the degradation efficiency was improved by 14%.


RSC Advances ◽  
2020 ◽  
Vol 10 (46) ◽  
pp. 27538-27551
Author(s):  
Qi Wang ◽  
Bihan Li ◽  
Ping Zhang ◽  
Wenming Zhang ◽  
Xiaoru Hu ◽  
...  

BPNs in the WO3–BPNs heterojunction acted as a co-catalyst to enhance photo-generated electron–hole pairs separation and improve degradation performance.


2014 ◽  
Vol 16 (33) ◽  
pp. 17748-17755 ◽  
Author(s):  
P. Sudhagar ◽  
Anitha Devadoss ◽  
Taeseup Song ◽  
P. Lakshmipathiraj ◽  
Hyungkyu Han ◽  
...  

Maximizing the Au nanoparticle decoration on TiO2nanowire through nitrogen doping for simultaneous enhancement in visible light scattering and electron–hole charge separation.


2020 ◽  
Author(s):  
Zhaoqing Li ◽  
Zhufeng Liu ◽  
Xiao Yang ◽  
Peng Chen ◽  
Lei Yang ◽  
...  

Abstract According to the composite design, a series of black TiO2/graphene composites were synthesized to improve its photocatalytic activity. TiO2 is generated in situ on the surface of graphene by a facile sol-gel method. The combination of graphene and TiO2 was beneficial for eliminating the opportunity of photogenerated electron-hole recombination due to the excellent conductivity of graphene. In the subsequent hydrogenation process, the self-doping Ti3+ was introduced accompanied by the crystallization of amorphous TiO2. The narrowed bandgap caused by self-doping Ti3+ enhanced the visible light absorption and make the composites appear black. Both of them improved the photocatalytic performance of the synthesized black TiO2/graphene composites. The band structure of the composite was analyzed by valence band XPS, revealing the reason for the high visible light catalytic performance of the composite. The results proved that the black TiO2/graphene composites synthesized show attractive potential for applications in environmental and energy issues.


Micromachines ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 66 ◽  
Author(s):  
Xinxin Zhao ◽  
Hua Yang ◽  
Ziming Cui ◽  
Xiangxian Wang ◽  
Zao Yi

Bi4Ti3O12 square plates were synthesized via a hydrothermal route, and their growth process was systematically investigated. Carbon quantum dots (CQDs) were prepared using glucose as the carbon source, which were then assembled on the surface of Bi4Ti3O12 square plates via a hydrothermal route with the aim of enhancing the photocatalytic performance. XRD (X-ray powder diffraction), SEM (scanning electron microscopy), TEM (transmission electron microscopy), UV-vis DRS (diffuse reflectance spectroscopy), XPS (X-ray photoelectron spectroscopy), FTIR (Fourier transform infrared spectroscopy), PL (photoluminescence) spectroscopy, EIS (electrochemical impedance spectroscopy) and photocurrent spectroscopy were used to systematically characterize the as-prepared samples. It is demonstrated that the decoration of CQDs on Bi4Ti3O12 plates leads to an increased visible light absorption, slightly increased bandgap, increased photocurrent density, decreased charge-transfer resistance, and decreased PL intensity. Simulated sunlight and visible light were separately used as a light source to evaluate the photocatalytic activity of the samples toward the degradation of RhB in aqueous solution. Under both simulated sunlight and visible light irradiation, CQDs@Bi4Ti3O12 composites with an appropriate amount of CQDs exhibit obviously enhanced photocatalytic performance. However, the decoration of excessive CQDs gives rise to a decrease in the photocatalytic activity. The enhanced photocatalytic activity of CQDs-modified Bi4Ti3O12 can be attributed to the following reasons: (1) The electron transfer between Bi4Ti3O12 and CQDs promotes an efficient separation of photogenerated electron/hole pairs in Bi4Ti3O12; (2) the up-conversion photoluminescence emitted from CQDs could induce the generation of additional electron/hole pairs in Bi4Ti3O12; and (3) the photoexcited electrons in CQDs could participate in the photocatalytic reactions.


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