Browse
Submit Data
Databases
API
Help

Dataset Information

43 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

CTAB-Assisted Fabrication of Bi₂WO₆ Thin Nanoplates with High Adsorption and Enhanced Visible Light-Driven Photocatalytic Performance.

ABSTRACT: Two-dimensional thin Bi₂WO₆ nanoplates have been fabricated using a cetyltrimethylammonium bromide (CTAB)-assisted hydrothermal method. We investigated the proposed formation mechanism based on the crystalline structures of the thin Bi₂WO₆ nanoplates. The high adsorption ability and excellent visible-light driven photocatalytic activities of the Bi₂WO₆ nanoplates were illustrated, in view of exposed (001) facets of nanoplates possessing faster separation of photo-generated charge carriers and increased catalytically active sites. Such a cost-effective way to obtain Bi₂WO₆ nanoplates offers new possibilities for the design of adsorptive semiconductor photocatalysts with strengthened photocatalytic activities.

SUBMITTER: Zhou Y

PROVIDER: S-EPMC6153929 | biostudies-literature | 2017 May

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

CTAB-Assisted Fabrication of Bi₂WO₆ Thin Nanoplates with High Adsorption and Enhanced Visible Light-Driven Photocatalytic Performance.

Zhou Yuxue Y Lv Pengfei P Meng Xiangdong X Tang Yanping Y Huang Pingping P Chen Xiaobing X Shen Xiaoshuang X Zeng Xianghua X

Molecules (Basel, Switzerland) 20170522 5

Two-dimensional thin Bi₂WO₆ nanoplates have been fabricated using a cetyltrimethylammonium bromide (CTAB)-assisted hydrothermal method. We investigated the proposed formation mechanism based on the crystalline structures of the thin Bi₂WO₆ nanoplates. The high adsorption ability and excellent visible-light driven photocatalytic activities of the Bi₂WO₆ nanoplates were illustrated, in view of exposed (001) facets of nanoplates possessing faster separation of photo-generated charge carriers and in ...[more]

PMID: 28531162

Similar Datasets

Insights on the Use of Carbon Additives as Promoters of the Visible-Light Photocatalytic Activity of Bi₂WO₆.

Project description:We have explored the impact of the incorporation of various amounts of carbons from varied physicochemical features as additives to Bi₂WO₆ for the photocatalytic degradation of a dye using simulated solar light. Data has revealed that the composition and acidic character of the carbon additive are important parameters in the performance of the Bi₂WO₆/carbon catalysts. The presence of a carbon additive improved the conversion of the dye, evidencing the occurrence of charge transfer reactions that involve radical mediated reactions. The catalysts prepared with 2 and 5 wt.% of carbon additive outperformed the bare semiconductor, despite the shielding effect of the carbon matrix. The acidic nature of the Bi₂WO₆/carbon catalysts governs the degradation pathway (due to the preferential adsorption of the dye), that proceeds via the deethylation of the auxochrome groups of the dye at short irradiation times, followed by the cleavage of the chromophore at long irradiation times. Regarding the characteristics of the carbons, the photocatalytic degradation rate is accelerated by carbons of acidic character and high oxygen content, whereas the porosity seems to play a minor role. The presence of the carbon additives also affects the toxicity of the treated solutions, rendering lower values after shorter irradiation periods.

| S-EPMC6384959 | biostudies-literature

Fabrication of Wide-Range-Visible Photocatalyst Bi2WO6-x nanoplates via Surface Oxygen Vacancies.

Project description:Bi2WO6 as a high visible-light-driven catalyst has been aroused broad interest. However, it can only be excitated by the light with λ < 450 nm and the solar energy utilization need to be improved. Here, the wide-range-visible photoresponse Bi2WO6-x nanoplates were fabricated by introducing surface oxygen vacancies through the controllable hydrogen reduction method. The visible photoresponse wavelength range is extended from 450 nm to more than 600 nm. In addition, the photocatalytic activity of Bi2WO6-x is also increased and is 2.1 times as high as that of pristine Bi2WO6. The extending of the photoresponse range and the enhancement of the photoactivity both can be attributed to the surface-oxygen-vacancy states. This is because surface-oxygen-vacancy states generated above and partly overlapping of with the valence band (VB) will result in the rising of valence band maximum (VBM), thus broadening the VB width. This approach is proposed to develop many types of wide-range-visible optical materials and to be applicable to many narrow and wide bandgap materials.

| S-EPMC4726091 | biostudies-literature

Synthesis and application of Bi2WO6 for the photocatalytic degradation of two typical fluoroquinolones under visible light irradiation.

Project description:Bismuth tungstate (Bi2WO6) was successfully synthesized by a method combining ultrasonic solvothermal treatment and high-temperature calcination. The products were affirmed by X-ray diffraction, scanning electron microscopy, UV-vis diffuse reflection spectroscopy, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy. The characterization results indicated that calcination could improve the crystallinity and visible light utilization capacity of Bi2WO6. The photodegradation experiments showed that Bi2WO6 calcined at 450 °C for 3 h exhibited better photocatalytic activity for the degradation of norfloxacin and enrofloxacin under visible light irradiation than the catalyst prepared without calcination or calcined at other temperatures. Meanwhile, the effects of the amount of 450-Bi2WO6, the initial concentration of targets, and the pH of the solutions on the degradation were studied. Under the optimal conditions, the removal ratios reached to 92.95% (for norfloxacin) and 94.58% (for enrofloxacin) within 75 min. Furthermore, h+ and ·O2 - were identified to affect the photodegradation process significantly, and the possible photocatalytic mechanism was proposed. The as-prepared sample was verified to possess good stability and reusability, suggesting its potential application prospect in the treatment of fluoroquinolone antibiotics.

| S-EPMC9070762 | biostudies-literature

A facile ultrasonic-assisted fabrication of nitrogen-doped carbon dots/BiOBr up-conversion nanocomposites for visible light photocatalytic enhancements.

Project description:A highly efficient novel photocatalyst consisting of nitrogen-carbon dots (N-CDs) and three-dimensional (3D) hierarchical BiOBr was synthesized via a simple ultrasonic-assisted method and used for the degradation of hazardous dyes. Deposition of N-CDs onto the surface of BiOBr was confirmed through structure and composition characterizations. The N-CDs/BiOBr composites exhibited superior activity for organic contaminant degradation under visible light and the 1 wt% N-CDs/BiOBr composite showed the highest degradation rate, indicating that N-CDs/BiOBr composites have great potential for application in mitigating hazardous contaminants. The N-CDs played an important role in improving the photocatalytic performance, owing to the enhancement of up-converted photoluminescence behavior as well as the efficient separation of photogenerated charge carriers originating from the intimately contacted interface. A possible photocatalytic mechanism was proposed based on the experimental results.

| S-EPMC5361154 | biostudies-literature

Hierarchical Bi2WO6/TiO2-nanotube composites derived from natural cellulose for visible-light photocatalytic treatment of pollutants.

Project description:A series of Bi2WO6/TiO2-nanotube (Bi2WO6/TiO2-NT) heterostructured composites were prepared by utilizing natural cellulose (e.g., laboratory filter paper) as the structural template. The obtained nanoarchitectonics, namely Bi2WO6/TiO2-NT nanocomposites, displayed three-dimensionally interwoven structures which replicated the initial cellulose template. The composite Bi2WO6/TiO2-NT nanotubes were formed by TiO2 nanotubes that uniformly anchored with Bi2WO6 nanoparticles of various densities on the surface. The composites exhibited improved photocatalytic activities toward the reduction of Cr(VI) and degradation of rhodamine B under visible light (λ > 420 nm), which were attributed to the uniform anchoring of Bi2WO6 nanoparticles on TiO2 nanotubes, as well as strong mutual effects and well-proportioned formation of heterostructures in between the Bi2WO6 and TiO2 phases. These improvements arose from the cellulose-derived unique structures, leading to an enhanced absorption of visible light together with an accelerated separation and transfer of the photogenerated electron-hole pairs of the nanocomposites, which resulted in increased effective amounts of photogenerated carriers for the photocatalytic reactions. It was demonstrated that the photoinduced electrons dominated the photocatalytic reduction of Cr(VI), while hydroxyl radicals and reactive holes contributed to the photocatalytic degradation of rhodamine B.

| S-EPMC9359189 | biostudies-literature

The three-dimensional flower-like Bi2WO6 assisted by ethanolamine through a microwave method for efficient photocatalytic activity.

Project description:The three-dimensional flower-like Bi2WO6 was synthesized through a one-step microwave method (the reaction temperature was 434 K and the reaction took 10 min) with the assistance of ethanolamine (EA). The prepared samples were characterized by X-ray diffraction, scanning electron microscopy, Fourier-transform infrared spectroscopy, ultraviolet-visible spectroscopy, PL, X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller analysis. Methyl orange was used as target pollutant to evaluate the photocatalysis property of samples. Furthermore, the influence of the mechanism of EA on the structure and catalytic performance of Bi2WO6 was discussed. The detailed characterizations revealed that the three-dimensional flower-like Bi2WO6 was successfully synthesized with the assistance of EA. The results confirmed that EA significantly influenced the morphology of Bi2WO6 products. The addition of EA can effectively alter the pressure of the reaction and improve the crystal phase and structure of Bi2WO6 photocatalysts, enhancing the photocatalytic activity of samples and improving the photocatalytic efficiency. EA can serve as an assembling agent and structure-directing agent resulting in the formation of flower-like architectures. With the increase of the amount of EA, the as-prepared Bi2WO6 sample gradually forms a flower-like structure, leading to a shorter time of light holes migrating to the surface of the catalyst. It makes the compound rate significantly decreased, and improves the photocatalytic efficiency of the sample.

| S-EPMC6458385 | biostudies-literature

The Structural, Photocatalytic Property Characterization and Enhanced Photocatalytic Activities of Novel Photocatalysts Bi₂GaSbO₇ and Bi₂InSbO₇ during Visible Light Irradiation.

Project description:In order to develop original and efficient visible light response photocatalysts for degrading organic pollutants in wastewater, new photocatalysts Bi₂GaSbO₇ and Bi₂InSbO₇ were firstly synthesized by a solid-state reaction method and their chemical, physical and structural properties were characterized. Bi₂GaSbO₇ and Bi₂InSbO₇ were crystallized with a pyrochlore-type structure and the lattice parameter of Bi₂GaSbO₇ or Bi₂InSbO₇ was 10.356497 Å or 10.666031 Å. The band gap of Bi₂GaSbO₇ or Bi₂InSbO₇ was estimated to be 2.59 eV or 2.54 eV. Compared with nitrogen doped TiO₂, Bi₂GaSbO₇ and Bi₂InSbO₇, both showed excellent photocatalytic activities for degrading methylene blue during visible light irradiation due to their narrower band gaps and higher crystallization perfection. Bi₂GaSbO₇ showed higher catalytic activity compared with Bi₂InSbO₇. The photocatalytic degradation of methylene blue followed by the first-order reaction kinetics and the first-order rate constant was 0.01470 min-1, 0.00967 min-1 or 0.00259 min-1 with Bi₂GaSbO₇, Bi₂InSbO₇ or nitrogen doped TiO₂ as a catalyst. The evolution of CO₂ and the removal of total organic carbon were successfully measured and these results indicated continuous mineralization of methylene blue during the photocatalytic process. The possible degradation scheme and pathway of methylene blue was also analyzed. Bi₂GaSbO₇ and Bi₂InSbO₇ photocatalysts both had great potential to purify textile industry wastewater.

| S-EPMC5456611 | biostudies-other

Tunable and sustainable photocatalytic activity of photochromic Y-WO3 under visible light irradiation.

Project description:Although photochromic and photocatalytic performance are the most significant features of WO3, the effects of photochromism on photocatalytic activities have not been investigated further. Herein, a novel gear-shaped WO3, with high coloration efficiency, fast reversibility, and remarkable photocatalytic performance was successfully prepared via a facile hydrothermal method. The influence of photochromic effects on its photocatalytic properties was evaluated under visible light irradiation. The results showed that the yellow WO3 sample exhibited higher photocatalytic efficiencies toward tetracycline hydrochloride (TCH), oxytetracycline (OTC), rhodamine B (RhB), and ciprofloxacin (CIP) (94.3%, 87.9%, 76%, and 68.6%, respectively, in 60 min). Further research found that the redox conversion between W6+ and W5+ played a key role in separating e-/h+ pairs. Importantly, the rapid and reversible conversion between W6+ and W5+ could be realized through light radiation or H2O2 treatment. Therefore, the gear-shaped WO3 possessed tunable and sustainable photocatalytic properties and maintained a high level of activity after recycling ten times under visible light irradiation. This work provides new insights into practical WO3 applications for environmental remediation based on photochromic regulation.

| S-EPMC8693858 | biostudies-literature

Effective Visible Light-Driven Photocatalytic Degradation of Ciprofloxacin over Flower-like Fe3O4/Bi2WO6 Composites.

Project description:Photocatalytic degradation of organic pollution is a vital path to deal with environmental problems. Here, a direct Z-scheme 2D/2D heterojunction of a Fe3O4/Bi2WO6 photocatalyst is fabricated for the degradation of ciprofloxacin by a self-assembly strategy. Furthermore, to characterize the morphology of the obtained composite photocatalysts, various kinds of characterization methods were employed like XRD, XPS, SEM, and TEM. It is indicated that the flower-like photocatalyst is composed of nanosheets. Comparable photocatalysts were prepared by controlling the hydrothermal temperature and the iron content. In the photocatalytic degradation of ciprofloxacin (CIP) in water, under visible light irradiation, FB-180 (synthesized at 180 °C with 4% iron content) presents approximately 99.7% degradation efficiency in only 15 min. Meanwhile, during photocatalytic degradation reactions, the Fe3O4/Bi2WO6 heterojunction also displayed excellent stability, which still kept above 90% degradation efficiency after five consecutive cycles. UV-Vis DRS and M-S analyses showed that the Fe3O4/Bi2WO6 catalyst has a strong visible light absorption capacity and the transfer pathway of photo-induced charge carriers. PL, EIS, and TPR showed that Fe3O4/Bi2WO6 has an efficient separation and transfer rate of the photo-generated carriers. ESR analysis proved that the superoxide radical (•O2 -) and hydroxyl radical (•OH) play a major role in the Fe3O4/Bi2WO6 photocatalytic system. This special 2D/2D heterojunction we proposed may have huge potential for marine pollution treatment by photocatalysis degradation with dramatically boosted activities.

| S-EPMC7818623 | biostudies-literature

Visible-Light-Driven AO7 Photocatalytic Degradation and Toxicity Removal at Bi-Doped SrTiO3.

Project description:In this study, Bi-doped SrTiO3 perovskites (Sr1-xBixTiO3, x = 0, 0.03, 0.05, 0.07 and 0.1) were synthesized using the solid-state method, characterized, and tested as photocatalysts in the degradation of the azo dye acid orange 7 (AO7) under visible light. The perovskites were successfully synthesized, and XRD data showed a predominant, well-crystallized phase, belonging to the cubic perovskite symmetry. For the doped samples, a minority phase, identified as bismuth titanate, was detected. All doped samples exhibited improved photocatalytic activity under visible light, on the degradation of AO7 (10 mg L-1), when compared with the undoped SrTiO3, with an increase in relative Abs484 nm decay from 3.7% to ≥67.8% after 1 h, for a powder suspension of 0.2 g L-1. The best photocatalytic activity was exhibited by the Sr0.95Bi0.05TiO3 perovskite. Reusability studies showed no significant loss in photocatalytic activity under visible light. The final solutions showed no toxicity towards D. magna, proving the efficiency of Sr0.95Bi0.05TiO3 as a visible-light-driven photocatalyst to degrade both the AO7 dye as well as its toxic by-products. A degradation mechanism is proposed.

| S-EPMC8999963 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data