scholarly journals Facile Green Synthesis of BiOBr Nanostructures with Superior Visible-Light-Driven Photocatalytic Activity

Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1273 ◽  
Author(s):  
Seema Garg ◽  
Mohit Yadav ◽  
Amrish Chandra ◽  
Sameer Sapra ◽  
Soniya Gahlawat ◽  
...  

Novel green bismuth oxybromide (BiOBr-G) nanoflowers were successfully synthesized via facile hydrolysis route using an Azadirachta indica (Neem plant) leaf extract and concurrently, without the leaf extract (BiOBr-C). The Azadirachta indica leaf extract was employed as a sensitizer and stabilizer for BiOBr-G, which significantly expanded the optical window and boosted the formation of photogenerated charge carriers and transfer over the BiOBr-G surface. The photocatalytic performance of both samples was investigated for the degradation of methyl orange (MO) and phenol (Ph) under the irradiation of visible light. The leaf extract mediated BiOBr-G photocatalyst displayed significantly higher photocatalytic activity when compared to BiOBr-C for the degradation of both pollutants. The degradation rate of MO and Ph by BiOBr-G was found to be nearly 23% and 16% more when compared to BiOBr-C under visible light irradiation, respectively. The substantial increase in the photocatalytic performance of BiOBr-G was ascribed to the multiple synergistic effects between the efficient solar energy harvesting, narrower band gap, high specific surface area, porosity, and effective charge separation. Furthermore, BiOBr-G displayed high stability for five cycles of photocatalytic activity, which endows its practical application as a green photocatalyst in the long run.

RSC Advances ◽  
2015 ◽  
Vol 5 (69) ◽  
pp. 56136-56144 ◽  
Author(s):  
Mengqiao Zang ◽  
Lei Shi ◽  
Lin Liang ◽  
Defeng Li ◽  
Jianmin Sun

The heterostructured g-C3N4/Ag–TiO2 composites exhibited high photocatalytic activity, which was attributed to the synergistic effects of the enhanced absorption of visible light and the efficient separation rates for photogenerated electrons-holes.


2019 ◽  
Vol 19 (6) ◽  
pp. 3343-3355 ◽  
Author(s):  
Ge Li ◽  
Bao-Dong Wang ◽  
Qi Sun ◽  
Wayne-Qiang Xu ◽  
Yi-Fan Han

Pure TiO2 nanoparticles and ones doped with Fe and/or Ni were successfully prepared by a co-precipitation method from ilmenite. The samples were structurally characterized by XRD, XPS, FT-IR, UV-vis, SEM, EDX, AAS and BET measurement. The XRD results showed that all samples were anatase TiO2, and no characteristic peaks of dopants were observed. The crystallite sizes of all doped TiO2 nanoparticles were less than 20 nm and doping TiO2 with metal ions can suppress the crystal growth of the particles. The XRD and XPS results indicated that TiO2 was uniformly doped and its crystalline phase was not changed by doping. The specific surface area of Fe–Ni/TiO2 is bigger than that of the un-doped TiO2. The pore size and pore volume of Fe–Ni/TiO2 is smaller than that of the un-doped. UV-vis spectra of the samples showed that the absorption edge red shifted with increasing doped metal content. The photocatalytic activity was evaluated in oxidative degradation of methylene blue (MB) with H2O2 under visible light irradiation. When doped with a single type of transition metal, the photocatalytic performance of Ni-doped samples was lower than that of Fe-doped ones. For the co-doped catalysts, the catalytic efficiency of 0.5%Fe4%Ni/TiO2 was the highest, reaching 93.34% after 250 min. Metal doping enhanced the photocatalytic decomposition of methylene blue compared with that of pure TiO2 by up to 1.5 times. The synergistic effects of the two metal ions improved the photocatalytic performance. The particles exhibited pronounced activity in degradation of MB as well as efficient recyclability. The photocatalytic degradation mechanism of methylene blue was analyzed.


2019 ◽  
Vol 8 (1) ◽  
pp. 56-61
Author(s):  
Aneeya K. Samantara ◽  
Debasrita Dash ◽  
Dipti L. Bhuyan ◽  
Namita Dalai ◽  
Bijayalaxmi Jena

: In this article, we explored the possibility of controlling the reactivity of ZnO nanostructures by modifying its surface with gold nanoparticles (Au NPs). By varying the concentration of Au with different wt% (x = 0.01, 0.05, 0.08, 1 and 2), we have synthesized a series of (ZnO/Aux) nanocomposites (NCs). A thorough investigation of the photocatalytic performance of different wt% of Au NPs on ZnO nanosurface has been carried out. It was observed that ZnO/Au0.08 nanocomposite showed the highest photocatalytic activity among all concentrations of Au on the ZnO surface, which degrades the dye concentration within 2 minutes of visible light exposure. It was further revealed that with an increase in the size of plasmonic nanoparticles beyond 0.08%, the accessible surface area of the Au nanoparticle decreases. The photon absorption capacity of Au nanoparticle decreases beyond 0.08% resulting in a decrease in electron transfer rate from Au to ZnO and a decrease of photocatalytic activity. Background: Due to the industrialization process, most of the toxic materials go into the water bodies, affecting the water and our ecological system. The conventional techniques to remove dyes are expensive and inefficient. Recently, heterogeneous semiconductor materials like TiO2 and ZnO have been regarded as potential candidates for the removal of dye from the water system. Objective: To investigate the photocatalytic performance of different wt% of Au NPs on ZnO nanosurface and the effect of the size of Au NPs for photocatalytic performance in the degradation process. Methods: A facile microwave method has been adopted for the synthesis of ZnO nanostructure followed by a reduction of gold salt in the presence of ZnO nanostructure to form the composite. Results: ZnO/Au0.08 nanocomposite showed the highest photocatalytic activity which degrades the dye concentration within 2 minutes of visible light exposure. The schematic mechanism of electron transfer rate was discussed. Conclusion: Raspberry shaped ZnO nanoparticles modified with different percentages of Au NPs showed good photocatalytic behavior in the degradation of dye molecules. The synergetic effect of unique morphology of ZnO and well anchored Au nanostructures plays a crucial role.


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.


2021 ◽  
Vol 50 (9) ◽  
pp. 3253-3260 ◽  
Author(s):  
Shan Zhao ◽  
Junbiao Wu ◽  
Yan Xu ◽  
Xia Zhang ◽  
Yide Han ◽  
...  

CdS/Ag2S/g-C3N4 ternary composites showed excellent photocatalytic performance toward H2 evolution. Their improved photocatalytic activity could be attributed not only to the synergic effect, but also to the introduction of Ag2S.


Minerals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 437 ◽  
Author(s):  
Zhiming Sun ◽  
Fang Yuan ◽  
Xue Li ◽  
Chunquan Li ◽  
Jie Xu ◽  
...  

A novel kind of cyanuric-acid-modified graphitic carbon nitride (g-C3N4)/kaolinite (m-CN/KA) composite with enhanced visible light-driven photocatalytic performance was fabricated through a facile two-step process. Rhodamine B (RhB) was taken as the target pollutant to study the photocatalytic performance of the synthesized catalysts. It is indicated that the cyanuric acid modification significantly enhanced photocatalytic activity under visible light illumination in comparison with the other reference samples. The apparent rate constant of m-CN/KA is almost 1.9 times and 4.0 times those of g-C3N4/kaolinite and bare g-C3N4, respectively. The superior photocatalytic performance of m-CN/KA could be ascribed, not only to the generation of abundant pore structure and reactive sites, but also to the efficient separation of the photogenerated electron-hole pairs. Furthermore, the possible photocatalytic degradation mechanism of m-CN/KA was also presented in this paper. It could be anticipated that this novel and efficient, metal-free, mineral-based photocatalytic composite has great application prospects in organic pollutant degradation.


2016 ◽  
Vol 45 (43) ◽  
pp. 17521-17529 ◽  
Author(s):  
Shuai-Ru Zhu ◽  
Peng-Fei Liu ◽  
Meng-Ke Wu ◽  
Wen-Na Zhao ◽  
Guo-Chang Li ◽  
...  

BiOBr/NH2-MIL-125(Ti) composite photocatalysts have been prepared by incorporating NH2-MIL-125(Ti) with BiOBr and exhibited improved photocatalytic activity under visible light compared to pristine BiOBr and NH2-MIL-125(Ti).


RSC Advances ◽  
2016 ◽  
Vol 6 (8) ◽  
pp. 6643-6650 ◽  
Author(s):  
Lijuan Han ◽  
Zheng Ma ◽  
Zhihe Luo ◽  
Gang Liu ◽  
Jiantai Ma ◽  
...  

The precursor with nanotubes structure can be hydrogenated easily in lower temperature comparing with nanobelts. The light absorption and photocatalytic activity of hydrogenated TiO2 nanotubes were enhanced drastically.


2017 ◽  
Vol 19 (36) ◽  
pp. 24915-24927 ◽  
Author(s):  
A. H. Reshak

The amalgamation of a wide optical band gap photocatalyst with visible-light-active CdO quantum dots (QDs) as sensitizers is one of the most efficient ways to improve photocatalytic performance under visible light irradiation.


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