278 research outputs found
Various Worshiping Traditions in Silapathikaram
Greetings and worship have been followed for many years, Tamil literature highlights that people have been living in different parts of the land and it can be seen that there were separate deities worshiped for each part of the land. In the inner life and in the outer life, the worship of the deity has achieved excellence and it can be known through the life and worship of the ancients. Rituals are associated with human culture. There is a belief among the people that the work undertaken after worshipping deities and the work will be successful and will end well. Thus, worships have become one of the cultural traditions. Silappathikaram is a versatile repository with many known news items. Considering the contribution to the history of Tamil Nadu during the Sangam period and the knowledge of the traditions followed by the Tamils, the multifaceted traditions of deity worship in Silapathikaram are examined in this article
Patterning of metal oxide thin films using a Hā/He atmospheric pressure plasma jet
A hydrogen-doped helium atmospheric pressure plasma jet (APPJ) is shown to be effective for the chemical reduction of metal oxides. Copper and tin oxide films (CuO and SnO2) show rapid (<2 seconds) and complete reduction to zero valence metal after exposure to the plasma jet, as revealed by X-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy, and Raman spectroscopy. After a total residence time of the plasma jet of 100 seconds, titanium oxide (TiO2) produced a surface decorated with Ti2+, Ti3+ and Ti4+ with proportions of 16, 38 and 46 atom%, respectively, as determined by XPS peak integration. Similarly, with tungsten oxide (WO3), after exposure for a few seconds, W5+ was produced, yielding a deep blue electrically conductive coating. The treatment of these oxide films by this dielectric radio frequency (RF) barrier discharge plasma jet provides a level of redox conversion not seen in any other technique, particularly for TiO2, especially with a comparable power input. The precise nature of the reduction is unclear; however, the involvement of free electrons may have an important role in the reduction process
Visible-Light-Active Iodide-Doped BiOBr Coatings for Sustainable Infrastructure
The search for efficient materials for sustainable infrastructure is an urgent challenge toward potential negative emission technologies and the global environmental crisis. Pleasant, efficient sunlight-activated coatings for applications in self-cleaning windows are sought in the glass industry, particularly those produced from scalable technologies. The current work presents visible-light-active iodide-doped BiOBr thin films fabricated using aerosol-assisted chemical vapor deposition. The impact of dopant concentration on the structural, morphological, and optical properties was studied systematically. The photocatalytic properties of the parent materials and as-deposited doped films were evaluated using the smart ink test. An optimized material was identified as containing 2.7 atom % iodide dopant. Insight into the photocatalytic behavior of these coatings was gathered from photoluminescence and photoelectrochemical studies. The optimum photocatalytic performance could be explained from a balance between photon absorption, charge generation, carrier separation, and charge transport properties under 450 nm irradiation. This optimized iodide-doped BiOBr coating is an excellent candidate for the photodegradation of volatile organic pollutants, with potential applications in self-cleaning windows and other surfaces
Surface mapping of photocatalytic activity in heterogeneous TiO2 films
Recent developments in advanced spectroscopy and imaging techniques are shedding light into key charge transfer processes and kinetics in photocatalysis. Complementary photocatalytic reactions with local markers and surface structural mapping are essential to establish property-function correlations in photocatalytic materials. The current work describes a simple approach to probe heterogeneous photocatalytic surfaces using digital colorimetry and the well-established smart ink test, based on the photo-induced reduction of resazurin dye. Surface crystallographic phase mapping is carried out using valence band photoemission spectra (depth resolution of ca. 5 nm). The method has prospective implementation to pixel-by-pixel analysis using high resolution cameras at micron scale
Iron-Intercalated Zirconium Diselenide Thin Films from the Low-Pressure Chemical Vapor Deposition of [Fe(Ī·āµ-Cā HāSe)āZr(Ī·āµ-Cā Hā )ā]ā
Transition metal chalcogenide thin films of the type FexZrSe2 have applications in electronic devices, but their use is limited by current synthetic techniques. Here, we demonstrate the synthesis and characterization of Fe-intercalated ZrSe2 thin films on quartz substrates using the low-pressure chemical vapor deposition of the single-source precursor [Fe(Ī·5-C5H4Se)2Zr(Ī·5-C5H5)2]2. Powder X-ray diffraction of the film scraping and subsequent Rietveld refinement of the data showed the successful synthesis of the Fe0.14ZrSe2 phase, along with secondary phases of FeSe and ZrO2. Upon intercalation, a small optical band gap enhancement (Eg(direct)opt = 1.72 eV) is detected in comparison with that of the host material
High Defect Nanoscale ZnO Films with Polar Facets for Enhanced Photocatalytic Performance
The fabrication of highly efficient photocatalytic thin films has important consequences for self-cleaning, organic pollutant decomposition, and antimicrobial coatings for a variety of applications. Here, we developed a simple synthesis method to produce efficient, high-surface-area zinc oxide (ZnO) photocatalytic films using aerosol-assisted chemical vapor deposition. This approach used mixtures of methanol and acetic acid to promote preferential growth and exposure of polar facets, which favor photocatalytic activity. Interestingly, the initial enhanced efficiency of the films was correlated to structural defects, likely oxygen vacancies, as supported by photoluminescence spectroscopy results. Discussion over the influence of such defects on photocatalytic performance is described, and the need for strategies to develop high-surface-area materials containing stable defects is highlighted
Corrigendum to: Influence of Lithium and Lanthanum Treatment on TiO 2 Nanofibers and Their Application in n-i-p Solar Cells (ChemElectroChem, (2019), 6, 14, (3590-3598), 10.1002/celc.201900532)
Correlative light and electron microscopy suggests that mutant huntingtin dysregulates the endolysosomal pathway in presymptomatic Huntingtonās disease
Huntingtonās disease (HD) is a late onset, inherited neurodegenerative disorder for which early pathogenic events remain poorly understood. Here we show that mutant exon 1 HTT proteins are recruited to a subset of cytoplasmic aggregates in the cell bodies of neurons in brain sections from presymptomatic HD, but not wild-type, mice. This occurred in a disease stage and polyglutamine-length dependent manner. We successfully adapted a high-resolution correlative light and electron microscopy methodology, originally developed for mammalian and yeast cells, to allow us to correlate light microscopy and electron microscopy images on the same brain section within an accuracy of 100 nm. Using this approach, we identified these recruitment sites as single membrane bound, vesicle-rich endolysosomal organelles, specifically as (1) multivesicular bodies (MVBs), or amphisomes and (2) autolysosomes or residual bodies. The organelles were often found in close-proximity to phagophore-like structures. Immunogold labeling localized mutant HTT to non-fibrillar, electron lucent structures within the lumen of these organelles. In presymptomatic HD, the recruitment organelles were predominantly MVBs/amphisomes, whereas in late-stage HD, there were more autolysosomes or residual bodies. Electron tomograms indicated the fusion of small vesicles with the vacuole within the lumen, suggesting that MVBs develop into residual bodies. We found that markers of MVB-related exocytosis were depleted in presymptomatic mice and throughout the disease course. This suggests that endolysosomal homeostasis has moved away from exocytosis toward lysosome fusion and degradation, in response to the need to clear the chronically aggregating mutant HTT protein, and that this occurs at an early stage in HD pathogenesis
Influence of Lithium and Lanthanum Treatment on TiO2 Nanofibers and Their Application in n-i-p Solar Cells
The addition of cations to TiO2 photoelectrodes is routinely accepted as a route to enhance the performance of conventional nāiāp solar cells. However, this is typically achieved in multiple steps or by the incorporation of expensive and hydroscopic cationic precursors such as lithium bis(trifluoromethanesulfonyl)imide. In addition, it is often unclear as to whether the incorporation of such cation sources is inducing ādopingā or simply transformed into cationic oxides on the surface of the photoelectrodes. In this study, TiO2 nanofibers were produced through a simple electrospinning technique and modified by introducing lithium and lanthanum precursors in one step. Our results show that the addition of both cations caused minimal substitutional or interstitial doping of TiO2. BrunauerāEmmettāTeller measurements showed that lanthanumātreated TiO2 nanofibers had an increase in surface area, which even exceeded that of TiO2 P25 nanoparticles. Finally, treated and untreated TiO2 nanofibers were used in nāiāp solar cells. Photovoltaic characteristics revealed that lanthanum treatment was beneficial, whereas lithium treatment was found to be detrimental to the device performance for both dyeāsensitized and perovskite solar cells. The results discuss new fundamental understandings for two of the commonly incorporated cationic dopants in TiO2 photoelectrodes, lithium and lanthanum, and present a significant step forward in advancing the field of materials chemistry for photovoltaics
Transparent superhydrophobic PTFE films via one-step aerosol assisted chemical vapor deposition
In this study, hierarchical micro/nano-structured transparent superhydrophobic polytetrafluoroethylene (PTFE) films showing a water contact angle (CA) of 168Ā°, a water sliding angle (SA) 90% were prepared on glass substrates via aerosol-assisted chemical vapor deposition (AACVD). Scanning electron microscopy showed the morphology to be rough, composed of both micro and nano sized protrusions. Mechanical testing showed that after impingement from 800 drops of 15 Ī¼L water (height = 1 m) or 10 g of sand grains (height = 65 cm), the CA of the transparent PTFE surface was still >150Ā°, still demonstrating excellent superhydrophobicity. The films also showed self-cleaning and anti-corrosion properties. This one-step fabrication is a facile way of producing various kinds of transparent superhydrophobic surfaces
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