Browse
Submit Data
Databases
API
Help

Dataset Information

15 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Elucidating the Photocatalytic Behavior of TiO₂-SnS₂ Composites Based on Their Energy Band Structure.

ABSTRACT: TiO₂-SnS₂ composite semiconducting photocatalysts with different building component ratios were prepared by hydrothermal synthesis (TiO₂-SnS₂-HT) and by immobilization of commercial TiO₂ and SnS₂ particles (TiO₂-SnS₂-COMM). The band gap values, which determine the catalysts’ photoactivity, were examined by diffuse reflectance spectroscopy and Kubelka⁻Munk transformations. The catalysts’ surface properties: specific surface area, charge and adsorption capacitance at the solid⁻solution interface were characterized using BET analysis, potentiometric titration and electrochemical impedance spectroscopy, respectively. The electronic band structure of TiO₂-SnS₂ photocatalyst, as the key property for the solar-driven photocatalysis, was deduced from the thermodynamic data and the semiconducting parameters (type of semiconductivity, concentration of the charge carriers, flat band potential) obtained by Mott⁻Schottky analysis. The photoactivity of both composites was studied in photocatalytic treatment of diclofenac (DCF) under simulated solar irradiation and was compared to the benchmark photocatalyst (TiO₂ P25) activity. The influence of process parameters, such as pH, H₂O₂, and composite formulation on the effectiveness of DCF removal and conversion was investigated and discussed by employing response surface modeling (RSM) approach. The photocatalytic efficiency of both composite materials was discussed on the basis of the hetereojunction formation that facilitated the photoelectron transfer, promoting more efficient photocatalytic degradation of DCF.

SUBMITTER: Kovacic M

PROVIDER: S-EPMC6024962 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Structure and Photocatalytic Properties of Mn-Doped TiO₂ Loaded on Wood-Based Activated Carbon Fiber Composites.

Project description:Mn-doped TiO₂ loaded on wood-based activated carbon fiber (Mn/TiO₂-WACF) was prepared by sol-gel and impregnation method using MnSO₄·H₂O as manganese source. The structure of Mn/TiO₂-WACF was characterized by SEM, XRD, FTIR, N₂ adsorption and UV-Vis, and its photocatalytic activity for methylene blue degradation was investigated. Results show that Mn-doped TiO₂ were loaded on the surface of wood-based activated carbon fiber with high-development pore structures. The crystallite sizes of Mn-doped TiO₂ in composites were smaller than that of the undoped samples. With an increase of Mn doping content, Ti-O bending vibration intensity of Mn/TiO₂-WACF increased and then decreased. Moreover, Ti-O-Ti and Ti-O-Mn absorption peaks increased upon doping of Mn. Mn/TiO₂-WACF with low specific surface area, and pore volume was improved at 3.5-6.0 nm of mesopore distributions due to the Mn-doped TiO₂ load. In addition, the UV-Vis showed that Mn/TiO₂-WACF (photodegradation rate of 96%) has higher photocatalytic activity than the undoped samples for methylene blue degradation under visible light irradiation.

| S-EPMC5554012 | biostudies-other

Preparation and Characterization of Zeolite/TiO? Cement-Based Composites with Excellent Photocatalytic Performance.

Project description:A zeolite/TiO? composite (ZTC) was applied to prepare a high-quality photocatalytic cement-based material (PCM). The acetone degradation experiment and micro measurements including XRD(X-Ray Diffractometer), SEM-EDS(Scanning Electron Microscope-Energy Dispersive Spectrometer), BET(BET Specific Surface Area Tester), FTIR(Fourier Transform Infrared Spectrometer) were conducted to characterize the photocatalytic efficiency and physicochemical properties of PCM, respectively. Results show that TiO? particles disperse on the surface of a PCM homogeneously and provide abundant active sites for photocatalytic reactions. Compared to a normal photocatalytic cement-based material (NPCM), the TiO? content of a PCM is lower and its photocatalytic efficiency is higher. The ZTC frees TiO? particles from the impacts of cement hydration products and increases the adsorption volume of acetone. The photocatalytic performance of the PCM was stable after repeated tests. Using the ZTC as a photocatalyst has a prominent effect on the photocatalytic performance of the PCM.

| S-EPMC6316990 | biostudies-other

TiO₂-Based Photocatalytic Geopolymers for Nitric Oxide Degradation.

Project description:This study presents an experimental overview for the development of photocatalytic materials based on geopolymer binders as catalyst support matrices. Particularly, geopolymer matrices obtained from different solid precursors (fly ash and metakaolin), composite systems (siloxane-hybrid, foamed hybrid), and curing temperatures (room temperature and 60 °C) were investigated for the same photocatalyst content (i.e., 3% TiO₂ by weight of paste). The geopolymer matrices were previously designed for different applications, ranging from insulating (foam) to structural materials. The photocatalytic activity was evaluated as NO degradation in air, and the results were compared with an ordinary Portland cement reference. The studied matrices demonstrated highly variable photocatalytic performance depending on both matrix constituents and the curing temperature, with promising activity revealed by the geopolymers based on fly ash and metakaolin. Furthermore, microstructural features and titania dispersion in the matrices were assessed by scanning electron microscopy (SEM) and energy dispersive X-ray (EDS) analyses. Particularly, EDS analyses of sample sections indicated segregation effects of titania in the surface layer, with consequent enhancement or depletion of the catalyst concentration in the active sample region, suggesting non-negligible transport phenomena during the curing process. The described results demonstrated that geopolymer binders can be interesting catalyst support matrices for the development of photocatalytic materials and indicated a large potential for the exploitation of their peculiar features.

| S-EPMC5456889 | biostudies-other

Continuously Improved Photocatalytic Performance of Zn2SnO4/SnO2/Cu2O Composites by Structural Modulation and Band Alignment Modification.

Project description:Improving the photocatalytic performance of multi-component photocatalysts through structural modulation and band alignment engineering has attracted great interest in the context of solar energy utilization and conversion. In our work, Zn2SnO4/SnO2 hierarchical architectures comprising nanorod building block assemblies were first achieved via a facile solvothermal synthesis route with lysine and ethylenediamine (EDA) as directing agents, and then chemically etched in NaOH solution to enlarge the surface area and augment active sites. The etched Zn2SnO4/SnO2 hierarchical architectures were further decorated by Cu2O nanoparticles though an in situ chemical deposition method based on band alignment engineering. In comparison with unetched Zn2SnO4/SnO2, the specific surface area of Zn2SnO4/SnO2/Cu2O hierarchical architectures became larger, and the responsive region and absorbance intensity became wider and higher in the whole visible-light range. Zn2SnO4/SnO2/Cu2O hybrid photocatalysts presented enormously improved visible-light photocatalytic behaviour for Rhodamine B (RhB) decomposition. The enhancement of photocatalytic behaviour was dominantly attributed to the synergy effect of the larger specific surface area, higher light absorption capacity, and more effective photo-induced charge carrier separation and migration. A proposed mechanism for the enormously promoted photocatalytic behaviour is brought forth on the basis of the energy-band structure combined with experimental results.

| S-EPMC6835881 | biostudies-literature

Synthesis of Shape-Tailored WO₃ Micro-/Nanocrystals and the Photocatalytic Activity of WO₃/TiO₂ Composites.

Project description:A traditional semiconductor (WO₃) was synthesized from different precursors via hydrothermal crystallization targeting the achievement of three different crystal shapes (nanoplates, nanorods and nanostars). The obtained WO₃ microcrystals were analyzed by the means of X-ray diffraction (XRD), scanning electron microscopy (SEM) and diffuse reflectance spectroscopy (DRS). These methods contributed to the detailed analysis of the crystal morphology and structural features. The synthesized bare WO₃ photocatalysts were totally inactive, while the P25/WO₃ composites were efficient under UV light radiation. Furthermore, the maximum achieved activity was even higher than the bare P25's photocatalytic performance. A correlation was established between the shape of the WO₃ crystallites and the observed photocatalytic activity registered during the degradation of different substrates by using P25/WO₃ composites.

| S-EPMC5502922 | biostudies-other

Structure sensitive photocatalytic reduction of nitroarenes over TiO 2.

Project description:It is a subject of exploration whether the phase pure anatase or rutile TiO2 or the band alignment due to the heterojunctions in the two polymorphs of TiO2 plays the determining role in efficacy of a photocatalytic reaction. In this work, the phase pure anatase and rutile TiO2 have been explored for photocatalytic nitroarenes reduction to understand the role of surface structures and band alignment towards the reduction mechanism. The conduction band of synthesized anatase TiO2 has been found to be more populated with electrons of higher energy than that of synthesized rutile. This has given the anatase an edge towards photocatalytic reduction of nitroarenes over rutile TiO2. The other factors like adsorption of the reactants and the proton generation did not play any decisive role in catalytic efficacy.

| S-EPMC5562743 | biostudies-literature

Origin of Charge Trapping in TiO2/Reduced Graphene Oxide Photocatalytic Composites: Insights from Theory.

Project description:Composites of titanium dioxide (TiO2) and reduced graphene oxide (RGO) have proven to be much more effective photocatalysts than TiO2 alone. However, little attention has been paid so far to the chemical structure of TiO2/RGO interfaces and to the role that the unavoidable residual oxygen functional groups of RGO play in the photocatalytic mechanism. In this work, we develop models of TiO2 rutile (110)/RGO interfaces by including a variety of oxygen functional groups known to be present in RGO. Using hybrid density functional theory calculations, we demonstrate that the presence of oxygen functional groups and the formation of interfacial cross-links (Ti-O-C covalent bonds and strong hydrogen bonds between TiO2 and RGO) have a major effect on the electronic properties of RGO and RGO-based composites. The electronic structure changes from semimetallic to semiconducting with an indirect band gap, with the lowest unoccupied band positioned below the TiO2 conduction band and largely localized on RGO oxygen and carbon orbitals, with some contributions of RGO-bonded Ti atoms. We suggest that this RGO-based lowest unoccupied band acts as a photoelectron trap and the indirect nature of the band gap hinders electron-hole recombination. These results can explain the experimentally observed extended lifetimes of photoexcited charge carriers in TiO2/RGO composites and the enhancement of photocatalytic efficiency of these composites.

| S-EPMC7007046 | biostudies-literature

Preparation and Characterization of Surface Photocatalytic Activity with NiO/TiO₂ Nanocomposite Structure.

Project description:This study achieved a nanocomposite structure of nickel oxide (NiO)/titanium dioxide (TiO₂) heterojunction on a TiO₂ film surface. The photocatalytic activity of this structure evaluated by decomposing methylene blue (MB) solution was strongly correlated to the conductive behavior of the NiO film. A p-type NiO film of high concentration in contact with the native n-type TiO₂ film, which resulted in a strong inner electrical field to effectively separate the photogenerated electron-hole pairs, exhibited a much better photocatalytic activity than the controlled TiO₂ film. In addition, the photocatalytic activity of the NiO/TiO₂ nanocomposite structure was enhanced as the thickness of the p-NiO film decreased, which was beneficial for the migration of the photogenerated carriers to the structural surface.

| S-EPMC5455623 | biostudies-other

Improved Photocatalytic Activity of Polysiloxane TiO2 Composites by Thermally Induced Nanoparticle Bulk Clustering and Dye Adsorption.

Project description:Fine control of nanoparticle clustering within polymeric matrices can be tuned to enhance the physicochemical properties of the resulting composites, which are governed by the interplay of nanoparticle surface segregation and bulk clustering. To this aim, out-of-equilibrium strategies can be leveraged to program the multiscale organization of such systems. Here, we present experimental results indicating that bulk assembly of highly photoactive clusters of titanium dioxide nanoparticles within an in situ synthesized polysiloxane matrix can be thermally tuned. Remarkably, the controlled nanoparticle clustering results in improved degradation photocatalytic performances of the material under 1 sun toward methylene blue. The resulting coatings, in particular the 35 wt % TiO2-loaded composites, show a photocatalytic degradation of about 80%, which was comparable to the equivalent amount of bare TiO2 and two-fold higher with respect to the corresponding composites not subjected to thermal treatment. These findings highlight the role of thermally induced bulk clustering in enhancing photoactive nanoparticle/polymer composite properties.

| S-EPMC8413002 | biostudies-literature

BiOCl/TiO2/diatomite composites with enhanced visible-light photocatalytic activity for the degradation of rhodamine B.

Project description:A BiOCl/TiO2/diatomite (BTD) composite was synthesized via a modified sol-gel method and precipitation/calcination method for application as a photocatalyst and shows promise for degradation of organic pollutants in wastewater upon visible-light irradiation. In the composite, diatomite was used as a carrier to support a layer of titanium dioxide (TiO2) nanoparticles and bismuth oxychloride (BiOCl) nanosheets. The results show that TiO2 nanoparticles and BiOCl nanosheets uniformly cover the surface of diatomite and bring TiO2 and BiOCl into close proximity. Rhodamine B was used as the target degradation product and visible light (λ > 400 nm) was used as the light source for the evaluation of the photocatalytic properties of the prepared BTD composite. The results show that the catalytic performance of the BTD composite under visible-light irradiation is much higher than that of TiO2 or BiOCl alone. When the molar ratio of BiOCl to TiO2 is 1:1 and the calcination temperature is 400 °C, the composite was found to exhibit the best catalytic effect. Through the study of the photocatalytic mechanism, it is shown that the strong visible-light photocatalytic activity of the BTD composite results mainly from the quick migration of photoelectrons from the conduction band of TiO2/diatomite to the surface of BiOCl, which promotes the separation effect and reduces the recombination rate of the photoelectron-hole pair. Due to the excellent catalytic performance, the BTD composite shows great potential for wide application in the field of sewage treatment driven by solar energy.

| S-EPMC6664401 | 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