VO2/TiO2 bilayer films for energy efficient windows with multifunctional properties

Vanadium dioxide/titanium dioxide bilayer films have been investigated as a thermochromic coating for application as intelligent window glazings for buildings. The nanostructured VO2 and TiO2 films were deposited on fluorine doped tin oxide coated glass substrates using electric field assisted aerosol assisted chemical vapour deposition (ElFi-AACVD) and sol-gel spin coating, respectively. Their thermochromic properties were investigated using scanning electron microscopy, X-ray diffraction, variable temperature UV/Vis/NIR and X-ray photoelectron spectroscopies. Compared to bare VO2 films, the VO2/TiO2 bilayer films exhibit an increase in visible light transmittance of up to 30%, an increase in integrated luminous transmisttance, with values up to 66%, and a higher transmittance modulation in the near infrared of up to 20% at the thermochromic transition temperature. The TiO2 top layer not only enhances visible light transmittance, but also serves to protect the VO2 bottom layer from oxidation. The bilayer films are shown to exhibit photo-induced super-hydrophilicity. These properties are affected by the morphology of the VO2 under-layer

Composition analysis of Ta3N5/W18O49 nanocomposite through XPS

A characterization of a nanocomposite material consisting of Ta3N5 nanoparticles and W18O49 nanowires is presented. The material is of interest for photocatalytic applications, with a focus on pollution reduction through the photodegradation of dye waste; under white light illumination, the combination of Ta3N5 and W18O49 yielded an enhanced rate of dye degradation relative to Ta3N5 particles alone. The facile method of synthesis is thought to be a promising route for both upscale and commercial utilization of the material. X-ray photoelectron spectroscopy revealed a core–shell composite structure with W18O49 present as an overlayer on Ta3N5; the analyzed spectra for the C 1s, O 1s, Ta 4f, N 1s, W 4f, and Na 1s regions are reported. It should be noted that due to differential charging of the underlying Ta3N5 component relative to the W18O49 shell, an additional uncompensated voltage shift may exist in the Ta 4f and N 1s spectra

A Clinical and Biological Guide for Understanding Chemotherapy-Induced Alopecia and its Prevention

Chemotherapy-induced alopecia (CIA) is the most visibly distressing side effect of commonly administered chemotherapeutic agents. As psychological health has huge relevance on lifestyle, diet and self-esteem, it is important for clinicians to fully appreciate the psychological burden that CIA can place on patients. Here, for the first time, we provide a comprehensive review encompassing the molecular characteristics of the human hair follicle (HF), how different anticancer agents damage the HF to cause CIA, subsequent HF pathophysiology and we assess known and emerging prevention modalities that have aimed to reduce or prevent CIA. We argue that, at present, scalp cooling is the only safe and FDA-cleared modality available, and we highlight the extensive available clinical and experimental (biological) evidence for its efficacy. The likelihood of a patient that uses scalp cooling during chemotherapy maintaining enough hair to not require a wig is approximately 50%. This is despite different types of chemotherapy regimens, patient-specific differences and possible lack of staff experience in effectively delivering scalp cooling. The increased use of scalp cooling and an understanding of how to deliver it most effectively to patients has enormous potential to ease the psychological burden of CIA, until other, more efficacious, equally safe treatments become available

Active removal of waste dye pollutants using Ta[sub]3N[sub]5/W[sub]18O[sub]49 nanocomposite fibres

A scalable solvothermal technique is reported for the synthesis of a photocatalytic composite material consisting of orthorhombic Ta3N5 nanoparticles and WOx≤3 nanowires. Through X-ray diffraction and X-ray photoelectron spectroscopy, the as-grown tungsten(VI) sub-oxide was identified as monoclinic W18O49. The composite material catalysed the degradation of Rhodamine B at over double the rate of the Ta3N5 nanoparticles alone under illumination by white light, and continued to exhibit superior catalytic properties following recycling of the catalysts. Moreover, strong molecular adsorption of the dye to the W18O49 component of the composite resulted in near-complete decolourisation of the solution prior to light exposure. The radical species involved within the photocatalytic mechanisms were also explored through use of scavenger reagents. Our research demonstrates the exciting potential of this novel photocatalyst for the degradation of organic contaminants, and to the authors’ knowledge the material has not been investigated previously. In addition, the simplicity of the synthesis process indicates that the material is a viable candidate for the scale-up and removal of dye pollutants on a wider scale

Structural and electronic properties of Cu4O3 (paramelaconite): the role of native impurities

Hybrid density functional theory has been used to study the phase stability and formation of native point defects in Cu4O3. This intermediate copper oxide compound, also known as paramelaconite, was observed to be difficult to synthesize due to stabilization issues between mixed-valence Cu1+ and Cu2+ ions. The stability range of Cu4O3 was investigated and shown to be realized in an extremely narrow region of phase space, with Cu2O and CuO forming readily as competing impurity phases. The origin of p-type conductivity is confirmed to arise from specific intrinsic copper vacancies occurring on the 1+ site. Away from the outlined stability region, the dominant charge carriers become oxygen interstitials, impairing the conductivity by creating deep acceptor states in the electronic band gap region and driving the formation of alternative phases. This study further demonstrates the inadequacy of native defects as a source of n-type conductivity and complements existing experimental findings

Nitrogen doping into titanium dioxide by the sol–gel method using nitric acid

N-doped TiO(2) has been prepared by use of sol-gel systems containing titanium alkoxide, with nitric acid as the nitrogen source. The time needed for gelation of the systems was drastically reduced by ultrasonic irradiation. The peaks assigned to the nitrate and nitrous ions were observed by FT-IR measurement during the sol-gel reaction. The N-doping was confirmed by the observation of N-O peaks in the XPS spectrum of the sample heated at 400 A degrees C. The nitrate ion acted as an oxidizer of the ethanol solvent and titanium species. The TiO(2) became doped with nitrogen oxide species as a result of reduction of nitrate ion incorporated into the dried gel samples. These results indicated that the added nitric acid was reduced during the sol-gel transition and heating process, and the resulting NO species were situated in the titania networks. The UV and visible photocatalytic activity of the samples was confirmed by the degradation of trichloroethylene.ArticleRESEARCH ON CHEMICAL INTERMEDIATES. 37(8):869-881 (2011)journal articl