Gotowa bibliografia na temat „TiO2-NTs”

Highly dispersed TiO2 nanotubes (TiO2-NTs) were synthesized via the reaction of anatase TiO2 powder with NaOH solution. Au nanoparticles of about 5 nm were deposited on the surface of TiO2-NTs with hydrothermal reduction method. The prepared nanocomposites were well characterized with TEM and XRD. Their photocatalytic properties and reducing ability were investigated by UV-Vis absorption and photocatalytic reduction of Cd2+ ions with different amount of TiO2-NTs and TiO2-NTs (Au) varying from 0.1g to 0.001g. The results from absorption patterns and AAS showed that the absorption intensity of TiO2-NTs (Au) was higher compared with that of TiO2-NTs. Moreover, the concentration of remanent Cd2+ (0.48mg/L) using TiO2-NTs (Au) was lower than that of Cd2+ (0.65mg/L) using TiO2-NTs.

AbstractHighly ordered TiO2 nanotube arrays (TiO2 NTs) were prepared by anodic oxidizing method on a surface of Ti substrate. Fabrication of nitrogen-doped TiO2 nanotube arrays (N-TiO2 NTs) was carried out by immersion in ammonia solution. CdS nanoparticles loaded N-doped TiO2 nanotube arrays (CdS/N-TiO2 NTs) were obtained by successive ionic layer adsorption and reaction (SILAR) technique. The samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), photoluminescence (PL) emission spectra and ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy (DRS). The results indicate that the TiO2 nanotube diameter and wall thickness are 100 nm to 120 nm and 20 nm to 30 nm, respectively. Moreover, the morphology and structure of the highly ordered TiO2 NTs are not affected by N-doping. Furthermore, CdS nanoparticles are evenly distributed on the surface of TiO2 NTs. Finally, the photocatalytic activity of CdS/N-TiO2 NTs was evaluated by degradation of MO under visible-light irradiation. Compared with TiO2 NTs, N-TiO2 NTs, CdS/N-TiO2 NTs exhibited enhanced photocatalytic properties, and the highest degradation rate of CdS/N-TiO2NTs could reach 97.6 % after 90 min of irradiation.

Novel Ag/TiO2-NTs composites have been synthesized using titanium dioxide nanotubes (TiO2-NTs) modified by (3-aminopropyl)trimethoxysilane (APS) as supports. The composites have been characterized by TEM and XRD. The better dispersion of Ag on TiO2-NTs modified by APS can be observed than that of TiO2-NTs without being modified by APS, which implies that APS is helpful for uniform nanoparticles. The electrocatalytic properties of Ag/TiO2-NTs for hydrazine oxidation were investigated in details. Excellent electrocatalytic activity was observed. The results showed that TiO2-NTs have a very good application potential as supporting materials for noble catalysts.

As a major indoor air pollutant, formaldehyde released from building and furnishing materials is one of the main volatile organic compounds (VOCs). Hierarchical TiO2 nanotube arrays (TiO2 NTs) prepared via a facile two-step anodization showed excellent photocatalytic (PC) degradation of formaldehyde at room temperature. Modification with noble metal nanoparticles (NMNs) could further improve the PC activity of TiO2 NTs. The final products of formaldehyde degradation were detected to be CO2 and H2O, which indicated that the mineralization of formaldehyde was the major process in this PC reaction. The reaction rate constants (k) determined for the three catalysts were in the order kTiO2 NTs < kAu/TiO2 NTs < kPt/TiO2 NTs (Pt/TiO2 NTs had the highest PC ability). The significant enhancement of PC performance can be ascribed to the formation of a Schottky junction between the NMNs and TiO2 NTs.

Photoelectrocatalytic degradation performance of hexachlorobenzene (HCB) was assessed with a newly designed continuous photocatalytic reactor. CdS/TiO2 NTs were successfully prepared by depositing CdS particles on the surface of TiO2 nanotube arrays.The morphology, phase structure and photoelectric properties of CdS/TiO2 NTs were characterized by field emission scanning electron microscope, X-ray diffraction and diffuse reflectance spectroscopy. The photoelectrocatalytic activity of CdS/TiO2 NTs was evaluated in degradation of HCB in aqueous solution. The experimental results show that CdS/TiO2 NTs exhibited higher photoabsorption rate under visible light, bigger photocurrent (value) and improved photocatalytic activity than TiO2 NTs.

γ-Fe2O3/N-doped TiO2 nanotubes (N-TiO2 NTs) photocatalyst was successfully prepared by a wet chemical method. Visible light responses of this novel catalyst for decomposing methyl orange (MO) in air were also evaluated. It was found that the photocatalytic activity of γ-Fe2O3/N-TiO2 NTs was higher than those of N-doped TiO2 NTs, TiO2 NTs and P25. The characterizations including TEM, EDX and UV/Vis DRS revealed that iron oxide nanoparticles were decorated in/around N-TiO2 NTs and the spectral response was enhanced in visible region. Meanwhile, the catalyst recycled by external magnetic field showed that its photocatalytic efficiency did not decrease obviously.

An electrochemical anodization is a simple and low cost technique, to electrochemically synthesize self-organized titanium dioxide (TiO2) nanotubes (NTs) from 1M Na2SO4 electrolyte with anodization of Ti foil. The FESEM results showed that the average diameter size and length of TiO2 NTs was found between 50 to 60 nm and 2.5 μm, respectively. The surface morphology of arrays TiO2 NTs is uniformly deposited on Ti substrate. While, the cross-sectional of TiO2 NTs revealed that, the TiO2 NTs is arrays alignment and close each other deposited. From current-anodisation time analysis (I-t) indicates that TiO2 nanotubes were start formed at anodisation time 429.03 sec with current flows is 51.69 mA in electrochemical system.

In this paper, reduced graphene oxide (RGO) was prepared by a modified Hummers method and chemical reduction method, and an RGO/TiO2 NTs (RGO/TiO2 nanotubes) photoelectrode was prepared by the electrochemical deposition method. The as-prepared RGO/TiO2 NTs were analyzed by scanning electron microscopy (SEM) and X-ray diffraction (XRD), and their photocatalytic activities were investigated by measuring the degradation of methylene blue (MB) under simulated solar light irradiation. The SEM and XRD results indicated that the original tubular structure of TiO2-NTs was not changed after RGO modification. The surface of the TiO2 NTs photoelectrode was covered with a non-uniform, flake-shaped reduced graphene oxide film. The thickness of the RGO/TiO2 NTs was increased to about 22.60 nm. The impedance of the RGO/TiO2 NTs was smaller than that of the TiO2 NT photoelectrode. The optimal preparation conditions of RGO/TiO2 NT photoelectrodes were investigated by using a single factor method and response surface method. The best preparation conditions were as follows: deposition potential at 1.19 V, deposition time of 10.27 min, and deposition temperature at 24.94 °C.

In this work, the calculated electron density difference, Bader charge analysis and the density of states (DOS) of SnO2–TiO2-nanotubes (NTs) indicate that the electrons are transferred from the Ti atoms of TiO2into the O atoms of (SnO[Formula: see text] in SnO2–TiO2-NTs and the supported (SnO[Formula: see text] cluster acts as the role of storage for photogenerated electrons excited from TiO2-NTs, which is in good agreement with experimental results that the SnO2–TiO2-NTs composite films have higher photocurrent density for photocathodic protection of 304 stainless steel (304SS). The theoretical investigations provide a plausible explanation for the photoelectrochemical anticorrosion mechanism of SnO2–TiO2-NTs using periodic density functional theory (DFT).

A novel type of TiO2 nanotubes (NTs)/Ag/MoS2 meshy photoelectrode was fabricated with highly oriented TiO2 nanotube arrays grown from a Ti mesh supporting Ag nanoparticles and three-dimensional MoS2 nanosheets. In this structure, Ag nanoparticles act as bridges to connect MoS2 and TiO2 and pathways for electron transfer, ensuring the abundant production of active electrons, which are the source of •O2−. The TiO2 NTs/Ag/MoS2 mesh can be used as both photocatalyst and electrode, exhibiting enhanced photoelectrocatalytic efficiency in degrading tetracycline hydrochloride under visible light irradiation (λ ≥ 420 nm). Compared to unmodified TiO2 NTs, the improved photoelectrocatalytic activity of the TiO2 NTs/Ag/MoS2 arise from the formation of Z-scheme heterojunctions, which facilitate the efficient separation of photogenerated electron-hole pairs through the Schottky barriers at the interfaces of TiO2 NTs–Ag and Ag–MoS2.

The present thesis discusses the beneficial effects of confining biologically relevant molecules inside porous structures of varying morphology and dimensions. Confinement of a biomolecule such as protein, enzymes drugs leads alteration in structural features and to a significant improvement in its biophysical properties. These properties include electrochemical redox behavior (for electroactive biomolecules) and thermal stability (denaturation temperature) of the concerned biomolecule. Silica (SiO2) based materials were primarily used as substrates for confining proteins and drugs. The confinement effects were probed in depth using various electrochemical, spectroscopic, and scattering techniques. The outcomes of confinement were utilized for developing electrochemical biosensors for the protein detection. Confinement of drugs effects their structural properties which gets reflected in their release kinetics studies. Electrochemical sensing was carried out using porous structure modified electrodes. These were used not only for detection of biological analytes but also extended to environmental pollutants. In the thesis, Chapters 2-4 deal with discussions related to electrochemical, spectroscopic, and scattering studies of protein confined inside SiO2 as well as polymer capsules. In Chapter 5A and 5B, Titania (TiO2) based nanotubes were utilized for demonstration of realistic electrochemical biosensors for the detection of myoglobin and a penicillin binding protein. In Chapters 6 and 7, enzyme and inhibitors, drug release kinetics from mesoporous oxides and TiO2 tubes have been discussed. Using the same approach as in chapter 5, electrochemical sensing of model environmental pollutants using TiO2 microwires have been discussed in chapters 8A and B. The use of TiO2 microwires for photocatalytic applications have also been considered in detail. A brief discussion of the contents and highlights of the individual chapters are described below: Chapter 1 discusses in detail about the porous substrates extensively used for biomolecular (proteins and drugs) confinement and structural features of these substrates. These substrates include the mesoporous materials of varying pore dimensions and pore arrangement. The alteration in the biophysical properties of the molecules because of confinement within these mesoporous substrates and its effects on related applications such as bio catalysis, drug release rates, electrochemical biosensing have been considered. A brief discussion on the present state of art in the field of drug delivery, enzyme catalysis and electrochemical biosensing have been included. The principles related to electrochemical, spectroscopic and the scattering techniques used to characterize the properties have been discussed in detail in this chapter. Chapter 2 include discussions on the investigations on the structure and function of hemoglobin (Hb) confined inside sol-gel template synthesized silica tubes (SiO2-tubes) Immobilization of hemoglobin inside SiO2-tubes resulted in the facile electron transfer to electroactive heme center leading to an enhanced electrochemical response. The consequences of confinement on protein structures and activity were further probed via ligand binding and thermal stability studies. Reversible binding of n-donor liquid ligands such as pyridine and its derivatives and predictive variation in their redox potentials were obtained from detailed electrochemical investigations. The results suggested absence of adverse effect on structure and function of Hb confined inside the channels of SiO2-tubes. Additionally, the thermal stability of confined Hb was compared to that of free Hb in solution. The melting or denaturation temperature of Hb immobilized inside SiO2-tubes increased by approximately 4 oC compared to that of free Hb. In Chapter 3A, the configuration of hemoglobin (Hb) in solution and confined inside silica tubes (SiO2-tubes) have been studied using synchrotron small angle x-ray scattering (SAXS) and the consequences were correlated to its electrochemical activity. Confinement inside silica tubes aided in preventing protein aggregation compared to that observed for unconfined protein in solution. In case of confined Hb, the radius of gyration (Rg) and size polydispersity (p) was considerably lower than in solution. The difference in configuration between the confined and unconfined protein were reflected in their electrochemical response. Reversible electrochemical response (from cyclic voltammograms) were obtained in case of the confined hemoglobin in contrary to only cathodic response for the unconfined protein in solution. This led to the conclusion of difference in orientation of the electroactive heme center. The electron transfer coefficient () and electron transfer rate constant (ks) were also calculated to further support the structural differences between the unconfined and confined states of the hemoglobin. Thus, absence of any adverse effects on confinement of proteins inside the inorganic matrices such as silica nanotubes opens new prospects for utilizing inorganic matrices as protein “encapsulators” as well as sensors at varying temperatures. Chapter 3B discusses the implications of host dimensions on the protein structure. This is a very important parameter as it considerably influences the protein properties under confinement. This study probes the structure of same Hb molecules, confined inside silica tubes of pore diameters varying by one order in magnitude: ~ 20-200 nm. The confinement effect on structure was probed vis-à-vis the protein in solution. Small angle neutron scattering (SANS), which provides information on the protein tertiary and quaternary structures, was employed to study the influence of tube pore diameter on confined protein structure and configuration. Depending on the SiO2-tubes pore diameter, confinement significantly influenced the structural stability of Hb. High radius of gyration (Rg) and polydispersity (p) of Hb in case of the 20 nm diameter SiO2-tubes indicated that Hb undergoes significant amount of aggregation. However, for SiO2-tubes with pore diameters > 100 nm, Rg of Hb was found to be in very close proximity to that obtained from the protein data bank (PDB) reported structure. This strongly indicated that the protein has a preference for the more native like non-aggregated state when confined inside tubes of diameter ~ 100 nm. Further insight in to the Hb structure was obtained from distance distribution function, p(R) and ab-initio models calculated from the SANS patterns. These also suggest that the size of SiO2-tubes is a key parameter for the protein stability and structure. In Chapter 4 we have introduced an organic substrate to investigate the effect of confinement on structure of hemoglobin (Hb). Like as discussed in chapters 3(A and B), Hb transformed from an aggregated state in solution to non-aggregated state when confined inside the polymer capsules. Synchrotron small angle x-ray scattering (SAXS) studies directly confirmed this fact. The radius of gyration (Rg) and polydispersity (p) of the proteins in the confined state were smaller compared to that in solution. In fact, the Rg value was very similar to theoretical values obtained using protein structures generated from protein databank. The Rg value was almost constant in the temperature range (25-85 °C, Tm = 59 °C), for the confined Hb. This observation is in contrary to the increasing Rg values obtained for the free Hb in solution suggesting higher thermal stability of confined Hb inside the polymer capsule. Protein functions gets significantly altered as a result this. It resulted in an enhancement of the electroactivity of confined Hb. While Hb in solution showed dominance of the cathodic process (Fe3+→ Fe2+), efficient reversible Fe3+/Fe2+ redox response is observed in case of the confined Hb. This again gave an indication of the difference in orientation of electroactive heme group resulting it to reside in a chemically different environment compared to when it is in solution. This has important implications on protein functional properties and related applications. Thus, in this chapter we get a detailed overview of how confinement orients different groups’ viz., electroactive heme center to take up positions that makes it favorable to participate in biochemical activities such as sensing of analytes from small to macromolecules and controlled delivery of drugs. The conclusions derived from the studies in previous chapters have been utilized in chapters 5A and 5B for developing a realistic electrochemical biosensor. Since the sensing based on electrochemical response largely depends on the location of heme group, the location of the heme center was altered in a controlled manner using chemical treatment. Chapter 5A deals with an alternate antibody-free strategy for the rapid electrochemical detection of cardiac myoglobin (having heme center) using hydrothermally synthesized TiO2 nanotubes (TiO2-NT). In this strategy, myoglobin was unfolded using denaturants to expose deeply buried electroactive heme center into the solution very close to the electrode. This leads to an efficient reversible electron transfer from protein to electrode surface. The sensing performance of the TiO2-NT modified electrodes were compared vis á vis commercially available titania and GCE electrodes. The tubular morphology of the TiO2-NT led to facile transfer of electrons to the electrode surface which eventually provided linear current response (obtained from cyclic voltammetry) over a wide range of Mb concentration. The sensitivity of the TiO2-NT based sensor was remarkable and was equal to 18 A/ mg ml-1 (detection limit= 50 nM). This coupled with the rapid analysis time of few tens of minutes (compared to few days for ELISA) demonstrates its potential usefulness for the early detection of the acute myocardial infarction (AMI). Chapter 5B comprises of a discussion of employing a rapid electrochemical detection method of proteins without any electroactive center. The protein was transformed to an electrochemically active protein via metal tagging (Fe3+ in this case). This biosensor was also based on titania (TiO2-NT) nanotubes which was used to modify the working electrode. To reduce the detection volumes drastically, screen printed carbon electrodes (SPCE) was introduced in this detection. It was possible to detect as low as 1 ng l-1 of protein in very small sample volumes (as low as 30 l). The feasibility of this method for the detection of PBP2a, a marker for methicillin resistant Staphylococcus aureus (MRSA) was demonstrated here. This biosensor could effectively detect PBP2a in whole cell lysate samples. To mimic the practical detection conditions, the selectivity and efficiency was also validated using other non-selective proteins such as PTP10D, a protein tyrosine phosphatase, and bovine serum albumin (BSA). As already mentioned, this electrochemical detection strategy could reproducibly detect protein samples within minutes compared to standard ELISA methods (3-4 h) or a modified ELISA protocols (FAST-ELISA; 30 mins) excluding the time taken for sample preparation. These observations suggest the potential of the titania nanotube based electrochemical biosensor in both clinical and community settings for the detection of infectious pathogen In Chapter 6, the feasibility of utilizing mesoporous matrices of alumina and silica for inhibition of enzymatic activity have been presented. These studies were performed on a protein tyrosine phosphatase by the name chick retinal tyrosine phosphotase-2 (CRYP- 2), a protein that is identical in sequence to the human glomerular epithelial protein-1 and involved in hepatic carcinoma. The inhibition of CRYP-2 is of tremendous therapeutic importance. Inhibition of catalytic activity was examined using the sustained delivery of para nitrocatechol sulfate (pNCS) from bare and amine functionalized mesoporous silica (MCM-48) and mesoporous alumina (Al2O3). Amine functionalized MCM-48 was found to exhibit the best release of pNCS among the various mesoporous matrices studied and hence inhibition of CRYP-2 was maximum in this case. The maximum speed of reaction, vmax (= 160 ± 10 μmols min-1mg-1) and inhibition constant, Ki (= 85.0 ± 5.0 μmols) estimated using a competitive inhibition model were found to be very similar to inhibition activities of protein tyrosine phosphatases using other methods. In Chapter 7, we have demonstrated another very attractive application of the TiO2-NT which have been already used for protein sensing application. Due to the porous nature of the surface and its other attractive features, TiO2-NT has a great potential in drug delivery applications. The TiO2-NT mimicked the pore channels of the mesoporous substrates that have been used in the previous chapter. The drug release from these TiO2- NT exhibited a completely different sigmoidal release profile compared to our previous reports from the group. Additionally, the effect of surface functionalization and solution pH on drug release profile have also been considered during our studies. The release profiles were modelled with theoretical Hill equation to extract several physical parameters to explain the extent of drug substrate interactions. These results further supplemented the unique nature of the release profile. In Chapter 8A we have again demonstrated an electrochemical detection strategy but this time for chemical pollutants. Commercial textile industry effluents such as dyes were chosen for the model studies. Mesoporous anatase titania microwires synthesized via an optimized polyol method were used for sensing and photocatalysis of these dyes. Using spectroscopic investigations, we have showed that these titania microwires preferentially sense cationic (e.g. methylene blue, Rhodamine B) over anionic (e.g. Orange G, Remazol Brilliant Blue R) dyes. It was observed that variation in microwire dimensions and pH of dye solution, led to an increase in the concentration of the adsorbed dye. These findings were later corroborated with much faster electrochemical sensing. The effect of microwire length on electrochemical detection sensitivity have also been accounted in these studies. The photochemical performance of these titania microwires have been compared with the commercial P25-TiO2 nano powders. The photochemical performance was also studied as a function of exposure times and pH of dye solution. Excellent sensing ability and photocatalytic activity of the titania microwires was attributed to increased effective reaction area of the controlled nanostructured morphology. This makes them an attractive substrate for commercial sensing applications In Chapter 8B, anatase TiO2 microwires used in previous chapter were chemically modified to silver (Ag) decorated TiO2 microwires (Ag-TiO2). This was done with an aim to improve the detection sensitivity and photodegradation performance. The Ag-TiO2 microwires were synthesized via polyol synthesis route followed by a simple surface modification and chemical reduction approach for attachment of silver. The electrochemical sensing performance of Ag-TiO2 microwires have been subsequently compared with the base TiO2 microwires in the detection of cationic dye such as methylene blue. The superior performance of the Ag-TiO2 composite microwires was attributed to improved surface reactivity, mass transport and catalytic property because of decorating the TiO2 surface with Ag nanoparticles. Further studies were also carried out to compare its photocatalytic activity with TiO2 microwires at constant illumination protocols and observation times. As demonstrated the improved photocatalytic performance of Ag-TiO2 composite microwires was attributed to the formation of a Schottky barrier between TiO2 and Ag nanoparticles leading to a fast transport of photogenerated electrons to the Ag nanoparticles.