760 research outputs found
Influence of the sodium/proton replacement on the structural, morphological and photocatalytic properties of titanate nanotubes
Titanate nanotubes (TNT) with different sodium contents have been synthesised
using a hydrothermal approach and a swift and highly controllable post-washing
processes. The influence of the sodium/proton replacement on the structural and
morphological characteristics of the prepared materials was analysed. Different
optical behaviour was observed depending on the Na+/H+ samples' content. A band
gap energy of 3.27\pm0.03 eV was estimated for the material with higher sodium
content while a value of 2.81\pm0.02 eV was inferred for the most protonated
material, which therefore exhibits an absorption edge in the near visible
region. The point of zero charge of the materials was determined and the
influence of the sodium content on the adsorption of both cationic and anionic
organic dyes was studied. The photocatalytic performance of the TNT samples was
evaluated in the rhodamine 6G degradation process. Best photodegradation
results were obtained when using the most protonated material as catalyst,
although this material has shown the lowest R6G adsorption capability.Comment: 22 pages, 8 figures, accepted for publication in Journal of
Photochemistry and Photobiology A: Chemistr
Synthesis of titanate nanostructures using amorphous precursor material and their adsorption/photocatalytic properties
This paper reports on a new and swift hydrothermal chemical route to prepare
titanate nanostructures (TNS) avoiding the use of crystalline TiO2 as starting
material. The synthesis approach uses a commercial solution of TiCl3 as
titanium source to prepare an amorphous precursor, circumventing the use of
hazardous chemical compounds. The influence of the reaction temperature and
dwell autoclave time on the structure and morphology of the synthesised
materials was studied. Homogeneous titanate nanotubes with a high
length/diameter aspect ratio were synthesised at 160^{\circ}C and 24 h. A band
gap of 3.06\pm0.03 eV was determined for the TNS samples prepared in these
experimental conditions. This value is red shifted by 0.14 eV compared to the
band gap value usually reported for the TiO2 anatase. Moreover, such samples
show better adsorption capacity and photocatalytic performance on the dye
rhodamine 6G (R6G) photodegradation process than TiO2 nanoparticles. A 98%
reduction of the R6G concentration was achieved after 45 minutes of irradiation
of a 10 ppm dye aqueous solution and 1 g/L of TNS catalyst.Comment: 29 pages, 10 figures, accepted for publication in Journal of
Materials Scienc
Multihierarchical electrodes based on titanate nanotubes and zinc oxide nanorods for photoelectrochemical water splitting
Multihierarchical electrodes based on titanate nanotubes and zinc oxide nanorods for photoelectrochemical water splitting
Studies involving water splitting to form hydrogen and oxygen have attracted attention because H2 is considered the fuel of the future. Photoelectrocatalysts have been widely used for this application, and several metal oxides can be applied as catalysts. Among them, we highlight zinc oxide nanorods (ZnONRs) and titanate nanotubes (TiNTs); however, their individual nanostructures exhibit disadvantages. For example, ZnONR shows rapid recombination of the photogenerated charges, and TiNT gives rise to randomly orientated films; these disadvantages limit their application as photoanodes. In this study, for the first time, we present a new class of multihierarchical electrodes based on TiNT-decorated ZnONR films that exhibited superior results to the individual species. The TiNTs are homogenously dispersed over the surface of the rods without forming agglomerates, giving rise to a heterojunction that exhibits lower recombination rates. It was found that the results are better when the contents of TiNT in the electrode are higher; thus, glycine was successfully used as a bridge to link both of the structures, increasing the amount of TiNT decorating the rods. As a result, the photocurrent generated with these multihierarchical electrodes is higher than that obtained for pure ZnONR electrodes (0.9 mA and 0.45 mA, respectively), and the electrode potentials for O2 evolution is lower than that observed for pure TiNT electrodes (0 V and 0.8 V vs. ERHE, respectively). The IPCE values are also higher for the multihierarchical electrodes
Extraction of Hydrophobic Analytes from Organic Solution into a Titanate 2D-Nanosheet Host: Electroanalytical Perspectives
Titanate nanosheets (single layer, typically 200 nm lateral size) deposited from aqueous colloidal solution onto electrode surfaces form lamellar hosts that bind redox active molecular redox probes. Here, hydrophobic redox systems such as anthraquinone, 1-amino-anthraquinone, deca-methylferrocene, 5,10,15,20-tetraphenyl-21H,23H-porphine manganese (III) chloride (TPPMnCl), and α-tocopherol are shown to bind directly from cyclopentanone solution (and from other types of organic solvents) into the titanate nanosheet film. For anthraquinone derivatives, stable voltammetric responses are observed in aqueous media consistent with 2-electron 2-proton reduction, however, independent of the pH of the outside solution phase environments. For decamethylferrocene a gradual decay of the voltammetric response is observed, but for TPPMnCl a more stable voltammetric signal is seen when immersed in chloride containing (NaCl) electrolyte. α-Tocopherol exhibits chemically irreversible oxidation and is detected with 1 mM–20 mM linear range and approximately 10 −3 M concentration limit of detection. All redox processes exhibit an increase in current with increasing titanate film thickness and with increasing external electrolyte concentration. This and other observations suggest that important factors are analyte concentration and mobility within the titanate host, as well as ion exchange between titanate nanosheets and the outside electrolyte phase to maintain electroneutrality during voltammetric experiments. The lamellar titanate (with embedded tetrabutyl-ammonium cations) behaves like a hydrophobic host (for hydrophobic redox systems) similar to hydrophobic organic microphase systems. Potential for analytical applications is discussed. </p
Titanate nanotubes for reinforcement of a poly(ethylene oxide)/chitosan polymer matrix
Photoelectroanalytical Oxygen Detection with Titanate Nanosheet – Platinum Hybrids Immobilised into a Polymer of Intrinsic Microporosity (PIM-1)
Stability and Electronic Properties of TiO2 Nanostructures With and Without B and N Doping
We address one of the main challenges to TiO2-photocatalysis, namely band gap
narrowing, by combining nanostructural changes with doping. With this aim we
compare TiO2's electronic properties for small 0D clusters, 1D nanorods and
nanotubes, 2D layers, and 3D surface and bulk phases using different
approximations within density functional theory and GW calculations. In
particular, we propose very small (R < 0.5 nm) but surprisingly stable
nanotubes with promising properties. The nanotubes are initially formed from
TiO2 layers with the PtO2 structure, with the smallest (2,2) nanotube relaxing
to a rutile nanorod structure. We find that quantum confinement effects - as
expected - generally lead to a widening of the energy gap. However,
substitutional doping with boron or nitrogen is found to give rise to
(meta-)stable structures and the introduction of dopant and mid-gap states
which effectively reduce the band gap. Boron is seen to always give rise to
n-type doping while depending on the local bonding geometry, nitrogen may give
rise to n-type or p-type doping. For under coordinated TiO2 surface structures
found in clusters, nanorods, nanotubes, layers and surfaces nitrogen gives rise
to acceptor states while for larger clusters and bulk structures donor states
are introduced
An Adaptable, Portable Microarray Reader for Biodetection
We have developed an inexpensive portable microarray reader that can be applied to standard microscope slide-based arrays and other array formats printed on chemically modified surfaces. Measuring only 19 cm in length, the imaging device is portable and may be applicable to both triage and clinical settings. For multiplexing and adaptability purposes, it can be modified to work with multiple excitation/emission wavelengths. Our device is shown to be comparable to a commercial laser scanner when detecting both streptavidin-biotin and antibody interactions. This paper presents the development and characterization of a handheld microarray imager and directly compares it with a commercial scanner
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