Browse
Submit Data
Databases
API
Help

Dataset Information

20 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Hollow ZnxCd1-xS nanospheres with enhanced photocatalytic activity under visible light.

ABSTRACT: Formation of solid solutions is a good strategy to acquire materials with special properties and bring forth new type of applications or enhance the performance of currently existing devices. In this study, hollow ZnxCd1-xS nanospheres with different molar ratios were synthesized via a facile hydrothermal process. The products were fully characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and UV-vis absorption spectroscopy. It was found that the photocatalysis performance of the as-prepared samples could be enhanced by formation of ZnxCd1-xS solid solutions. In addition, their photocatalytic activities are dependent on the Zn/Cd molar ratios and nanostructures of ZnxCd1-xS solid solutions. Hollow Zn0.2Cd0.8S spheres exhibit extremely high photocatalytic activity and good re-usability, and the photocatalytic conversion of RhB reaches as high as 96% after 50 min of irradiation.

SUBMITTER: Jin Y

PROVIDER: S-EPMC4957231 | biostudies-literature | 2016 Jul

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Hollow ZnxCd1-xS nanospheres with enhanced photocatalytic activity under visible light.

Jin Ying Y Zhang Haoyun H Song Chuang C Wang Lanfang L Lu Qingyi Q Gao Feng F

Scientific reports 20160722

Formation of solid solutions is a good strategy to acquire materials with special properties and bring forth new type of applications or enhance the performance of currently existing devices. In this study, hollow ZnxCd1-xS nanospheres with different molar ratios were synthesized via a facile hydrothermal process. The products were fully characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and UV-vis absorption ...[more]

PMID: 27444737

Similar Datasets

Hydrothermal Synthesis of Bismuth Ferrite Hollow Spheres with Enhanced Visible-Light Photocatalytic Activity.

Project description:In recent years, semiconductor hollow spheres have gained much attention due to their unique combination of morphological, chemical, and physico-chemical properties. In this work, we report for the first time the synthesis of BiFeO3 hollow spheres by a facile hydrothermal treatment method. The mechanism of formation of pure phase BiFeO3 hollow spheres is investigated systematically by variation of synthetic parameters such as temperature and time, ratio and amount of precursors, pressure, and calcination procedures. The samples were characterized by X-ray powder diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, and UV-vis diffuse reflectance spectroscopy. We observe that the purity and morphology of the synthesized materials are very sensitive to synthesis parameters. In general, the chemically and morphologically very robust hollow spheres have diameters in the range of 200 nm to 2 μm and a wall thickness of 50-200 nm. The synthesized BiFeO3 hollow spheres were applied as catalysts in the photodegradation of the model pollutant Rhodamine B under visible-light irradiation. Notably, the photocatalyst demonstrated exceptionally high removal efficiencies leading to complete degradation of the dye in less than 150 min at neutral pH. The superior efficiencies of the synthesized material are attributed to the unique features of hollow spheres. The active species in the photocatalytic process have been identified by trapping experiments.

| S-EPMC10343919 | biostudies-literature

Biofabricated BiOI with enhanced photocatalytic activity under visible light irradiation.

Project description:In the recent past, there has been a large-scale utilization of plant extracts for the synthesis of various photocatalysts. The biofabrication technology eliminates the usage of harmful chemicals and serves as an eco-friendly approach for environmental remediation. Herein, a comparative analysis between bismuth oxyiodide synthesized via Azadirachta indica (neem) leaf extract (BiOI-G) and without leaf extract (BiOI-C) has been envisaged. The BiOI-G and BiOI-C samples were characterized by spectral and microscopic techniques, which revealed that the Azadirachta indica assisted BiOI-G attained enhanced features over BiOI-C such as narrower band gap, large surface area, porosity, increased absorption range of visible light and effectual splitting of the photogenerated e--h+ pairs. Benefiting from these enhanced features, BiOI-G degraded methyl orange (MO), rhodamine B (RhB), and benzotriazole (BT) at a significantly higher rate in comparison to BiOI-C. The degradation rate of MO, RhB and BT by BiOI-G was observed to be 1.3, 1.25 and 1.29 times higher in comparison to BiOI-C. Moreover, BiOI-G displayed high stability upto five cycles of the photocatalytic activity, which endow its effectiveness as a highly-efficient green photocatalyst.

| S-EPMC9084558 | biostudies-literature

Non-Stacked γ-Fe2O3/C@TiO2 Double-Layer Hollow Nanoparticles for Enhanced Photocatalytic Applications under Visible Light.

Project description:Herein, a non-stacked γ-Fe2O3/C@TiO2 double-layer hollow nano photocatalyst has been developed with ultrathin nanosheets-assembled double shells for photodegradation phenol. High catalytic performance was found that the phenol could be completely degraded in 135 min under visible light, due to the moderate band edge position (VB at 0.59 eV and CB at -0.66 eV) of the non-stacked γ-Fe2O3/C@TiO2, which can expand the excitation wavelength range into the visible light region and produce a high concentration of free radicals (such as ·OH, ·O2-, holes). Furthermore, the interior of the hollow composite γ-Fe2O3 is responsible for charge generation, and the carbon matrix facilitates charge transfer to the external TiO2 shell. This overlap improved the selection/utilization efficiency, while the unique non-stacked double-layered structure inhibited initial charge recombination over the photocatalysts. This work provides new approaches for photocatalytic applications with γ-Fe2O3/C-based materials.

| S-EPMC8779976 | biostudies-literature

Enhanced Visible-Light Photocatalytic Activity of Bismuth Ferrite Hollow Spheres Synthesized via Evaporation-Induced Self-Assembly.

Project description:Semiconductor hollow spheres have garnered significant attention in recent years due to their unique structural properties and enhanced surface area, which are advantageous for various applications in catalysis, energy storage, and sensing. The present study explores the surfactant-assisted synthesis of bismuth ferrite (BiFeO3) hollow spheres, emphasizing their enhanced visible-light photocatalytic activity. Utilizing a novel, facile, two-step evaporation-induced self-assembly (EISA) approach, monodisperse BiFeO3 hollow spheres were synthesized with a narrow particle size distribution. The synthesis involved Bi/Fe citrate complexes as precursors and the triblock copolymer Pluronic P123 as a soft template. The BiFeO3 hollow spheres demonstrated outstanding photocatalytic performance in degrading the emerging pollutants Rhodamine B and metronidazole under visible-light irradiation (100% degradation of Rhodamine B in <140 min and of metronidazole in 240 min). The active species in the photocatalytic process were identified through trapping experiments, providing crucial insights into the mechanisms and efficiency of semiconductor hollow spheres. The findings suggest that the unique structural features of BiFeO3 hollow spheres, combined with their excellent optical properties, make them promising candidates for photocatalytic applications.

| S-EPMC11314036 | biostudies-literature

Enhanced photocatalytic activity of Se-doped TiO2 under visible light irradiation.

Project description:Anatase TiO2 is a typical photocatalyst, and its excellent performance is limited in ultraviolet light range due to its wide band gap of 3.2?eV. A series of Se-doped TiO2 nanoparticles in anatase structure with various Se concentrations up to 17.1?at.% were prepared using sol-gel method. The doped Se ions are confirmed to be mainly in the valence state of?+?4, which provides extra electronic states in the band gap of TiO2. The band gap is effectively narrowed with the smallest gap energy of 2.17?eV, and the photocatalytic activity is effectively improved due to the extended absorption range. The photocatalytic activity was evaluated by the degradation of Rhodamine B (RhB) in aqueous solution under visible light irradiation. The results show that Se doping significantly improves the photocatalytic activity of TiO2 and 13.63?at.% Se-doped TiO2 has the best performance.

| S-EPMC5993730 | biostudies-literature

Au nanoparticle-decorated TiO2 hollow fibers with enhanced visible-light photocatalytic activity toward dye degradation.

Project description:TiO2 hollow fibers (THF) were prepared by a template method using kapok as a biotemplate and subsequently decorated by plasmonic Au nanoparticles using a solution plasma process. The THF exhibited an anatase phase and a hollow structure with a mesoporous wall. Au nanoparticles with a diameter of about 5-10 nm were uniformly distributed on the THF surface. Au nanoparticles-decorated TiO2 hollow fibers (Au/THF) have enhanced photocatalytic activity toward methylene blue degradation under visible light-emitting diode (Vis-LED) as compared to pristine THF and P25. This could be attributed to combined effects including effective light-harvesting by a hollow structure, large surface area due to a mesoporous wall of THF, and visible-light absorption and efficient charge separation induced by Au nanoparticles. The Au/THF also showed good recyclability and separation ability.

| S-EPMC8978662 | biostudies-literature

Facile Synthesis of SrCO₃-Sr(OH)₂/PPy Nanocomposite with Enhanced Photocatalytic Activity under Visible Light.

Project description:Pyrrole monomer was chemically polymerized onto SrCO₃-Sr(OH)₂ powders to obtain SrCO₃-Sr(OH)₂/polypyrrole nanocomposite to be used as a candidate for photocatalytic degradation of methylene blue dye (MB). The material was characterized by Fourier transform infrared (FTIR) spectroscopy, UV/Vis spectroscopy, and X-ray diffraction (XRD). It was observed from transmission electronic microscopy (TEM) analysis that the reported synthesis route allows the production of SrCO₃-Sr(OH)₂ nanoparticles with particle size below 100 nm which were embedded within a semiconducting polypyrrole matrix (PPy). The SrCO₃-Sr(OH)₂ and SrCO₃-Sr(OH)₂/PPy nanocomposites were tested in the photodegradation of MB dye under visible light irradiation. Also, the effects of MB dye initial concentration and the catalyst load on photodegradation efficiency were studied and discussed. Under the same conditions, the efficiency of photodegradation of MB employing the SrCO₃-Sr(OH)₂/PPy nanocomposite increases as compared with that obtained employing the SrCO₃-Sr(OH)₂ nanocomposite.

| S-EPMC5456521 | biostudies-literature

Enhanced Photocatalytic Fuel Denitrification over TiO2/?-Fe2O3 Nanocomposites under Visible Light Irradiation.

Project description:With increasingly stringent environmental regulations, the removal of nitrogen-containing compounds (NCCs) from gasoline fuel has become a more and more important research subject. In this work, we have successfully synthesized TiO2/?-Fe2O3 heterogeneous photocatalysts with different mass ratios of TiO2 vs. ?-Fe2O3. Taking photocatalytic denitrification of typical alkali NCCs, pyridine, in gasoline fuel under visible light irradiation (????420?nm) as the model reaction, the TiO2/?-Fe2O3 hybrids have exhibited enhanced photocatalytic activity compared with pure TiO2 and ?-Fe2O3, giving a pyridine removal ratio of ?100% after irradiation for 240?min. The improved photocatalytic performance can be attributed to the integrative effect of the enhanced light absorption intensity and more efficient separation of photogenerated electron-hole pairs. Importantly, this type of heterogeneous photocatalysts can be easily separate in the reaction medium by an external magnetic field that is very important for industrial purpose. In addition, major reaction intermediates have been identified by the liquid chromatograph-mass spectrometer (HPLC-MS) and a tentative photocatalytic denitrification mechanism has been proposed.

| S-EPMC5552819 | biostudies-other

Ag3PO4/NiO Composites with Enhanced Photocatalytic Activity under Visible Light.

Project description:Black NiO powders were prepared by a hydrothermal method. Moreover, the visible light-driven Ag3PO4/NiO photocatalyst composites were successfully synthesized by in situ precipitation method. These samples were structurally characterized by X-ray diffraction and Rietveld refinement. The strong interaction between the phases and the defects in the samples was affected by the formation of the composites, as identified by Fourier transform infrared spectroscopy and Raman spectroscopy. UV-vis diffuse reflectance spectroscopy exhibited enhanced light absorption for all Ag3PO4/NiO composites, suggesting the effective interaction between the phases. Moreover, field-emission scanning electron microscopy images revealed the presence of NiO microflowers composed of nanoflakes in contact with Ag3PO4 microparticles. The composite with 5% NiO presented enhanced photocatalytic efficiency in comparison with pure Ag3PO4, degrading 96% of rhodamine B (RhB) dye in just 15 min under visible light; however, the recycling experiments confirmed that the composite with 75% NiO showed superior stability. The recombination of the electron-hole pairs was considered for the measurement of the photoluminescence of the samples. These measurements were performed to evaluate the possible causes for the difference in the photocatalytic responses of the composites. From these experimental results, possible photocatalytic mechanisms for RhB degradation over Ag3PO4/NiO composites under visible-light irradiation were proposed.

| S-EPMC7469368 | biostudies-literature

Enhanced photocatalytic activity of TiO2/UiO-67 under visible-light for aflatoxin B1 degradation.

Project description:TiO2 has great potential in photocatalytic degradation of organic pollutants, but poor visible light response and low separation efficiency of photogenerated electron-hole pairs limit its wide applications. In this study, we have successfully prepared TiO2/UiO-67 photocatalyst through an in situ solvothermal method. The degradation rate of aflatoxin B1 (AFB1) is 98.9% in only 80 min, which is superior to the commercial P25, commercial TiO2 and most of reported photocatalysts under visible light irradiation. In addition, the TiO2/UiO-67 photocatalyst showed excellent recyclability. We demonstrated that the enhanced photocatalytic mechanism was owing to the heterojunction between TiO2 and UiO-67, which enhanced effectively the separation photogenerated charge carriers and visible light response. The free radical trapping tests demonstrated that superoxide radicals (˙O2 -), holes (h+) and hydroxyl radicals (˙OH) were the main active species and then oxidized AFB1 to some small molecules.

| S-EPMC8982250 | 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