| 1. |
- Nagaraja, Ch., et al.
(författare)
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Opening remarks
- 2016
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Konferensbidrag (refereegranskat)
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| 2. |
- Kaur, A., et al.
(författare)
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Correlation between reduced dielectric loss and charge migration kinetics in NdFeO3-modified Ba0.7Sr0.3TiO3 ceramics
- 2021
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Ingår i: Journal of materials science. Materials in electronics. - : Springer Nature. - 0957-4522 .- 1573-482X. ; 32:20, s. 24910-24929
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Tidskriftsartikel (refereegranskat)abstract
- The present study demonstrates the reduction in the dielectric loss at room temperature from 0.149 to 0.027 in the composite of (NdFeO3)0.1−(Ba0.7Sr0.3TiO3)0.9 as compared to the undoped Ba0.7Sr0.3TiO3 and correlates with the charge compensation due to the ionic substitutions for both A site (NdBa) and B (FeTi) site generated excess electrons, localized hole states and robust oxygen vacancies (VO) along with different cationic oxidation states. The VO mediated F center charge transfer mechanism i.e., bound magnetic polaronic behaviour and defect complex generated between acceptors and ionized VO reduce electrical conductivity and loss factor. The presence of weak ferromagnetism in the M-H loop reconfirms the F center exchange mechanism in mixed phase symmetry. The activation energy calculated from impedance spectroscopy, electrical modulus and electrical conductivity analysis supports the presence of doubly ionized VO. Further, density functional theory based first principle calculation manifests that the impurity induced depopulation of valence band edge electrons into a single spin up channel which distorts TiO6 octahedra with fluctuating bond length and Ti 3deg orbital splitting observed in decomposed density of states for accommodating excess electrons. These trapped and accommodated electrons reduce the effective electron concentration which in turn decreases the electrical conductivity and loss factor.
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| 3. |
- Davies, Katherine Rebecca, et al.
(författare)
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Photoelectrocatalytic Surfactant Pollutant Degradation and Simultaneous Green Hydrogen Generation
- 2023
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Ingår i: Industrial & Engineering Chemistry Research. - 1520-5045 .- 0888-5885. ; In Press
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Tidskriftsartikel (refereegranskat)abstract
- For the first time, we demonstrate a photoelectrocatalysistechniquefor simultaneous surfactant pollutant degradation and green hydrogengeneration using mesoporous WO3/BiVO4 photoanodeunder simulated sunlight irradiation. The materials properties suchas morphology, crystallite structure, chemical environment, opticalabsorbance, and bandgap energy of the WO3/BiVO4 films are examined and discussed. We have tested the anionic type(sodium 2-naphthalenesulfonate (S2NS)) and cationic type surfactants(benzyl alkyl dimethylammonium compounds (BAC-C12)) as model pollutants.A complete removal of S2NS and BAC-C12 surfactants at 60 and 90 min,respectively, by applying 1.75 V applied potential vs RHE to the circuit,under 1 sun was achieved. An interesting competitive phenomenon forphotohole utilization was observed between surfactants and adsorbedwater. This led to the formation of H2O2 fromwater alongside surfactant degradation (anode) and hydrogen evolution(cathode). No byproducts were observed after the direct photoholemediated degradation of surfactants, implying its advantage over otherAOPs and biological processes. In the cathode compartment, 82.51 mu mol/cm(2) and 71.81 mu mol/cm(2) of hydrogen gas weregenerated during the BAC-C12 and S2NS surfactant degradation process,respectively, at 1.75 V RHE applied potential.
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| 4. |
- Davies, Katherine Rebecca, et al.
(författare)
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Solar light-driven simultaneous pharmaceutical pollutant degradation and green hydrogen production using a mesoporous nanoscale WO 3 /BiVO 4 heterostructure photoanode
- 2023
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Ingår i: Journal of Environmental Chemical Engineering. - 2213-3437 .- 2213-2929. ; 11:3
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Tidskriftsartikel (refereegranskat)abstract
- Photoelectrocatalysis is one of the most favourable techniques that could be used in this remit as it has the potential to utilise natural sunlight to generate oxidants in situ to mediate effective pollutant degradation. This work, therefore, utilises a mesoporous nanoscale WO3/BiVO4 heterostructure photoanode to effectively degrade ibuprofen in wastewater combined with simultaneous green hydrogen generation at the cathode under simulated sunlight. A near complete degradation (>96%) of ibuprofen (starting concentration of 100 mg/L), with no hazardous intermediates (determined via mass spectrometry analysis), along with simultaneous H2 evolution of 114 µmol/cm2 after 145 min was demonstrated in this work. In addition, intermediate product analysis, the role of the type of in situ oxidants on degradation, the mechanistic pathway of degradation, and the material characteristics of mesoporous photoanode were also investigated. First experimental evidence of in situ generated H2O2 contributing to the degradation of ibuprofen is presented.
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| 5. |
- Mestre, Humberto, et al.
(författare)
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Aquaporin-4-dependent glymphatic solute transport in the rodent brain
- 2018
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Ingår i: eLife. - 2050-084X. ; 7
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Tidskriftsartikel (refereegranskat)abstract
- The glymphatic system is a brain-wide clearance pathway; its impairment contributes to the accumulation of amyloid-β. Influx of cerebrospinal fluid (CSF) depends upon the expression and perivascular localization of the astroglial water channel aquaporin-4 (AQP4). Prompted by a recent failure to find an effect of Aqp4 knock-out (KO) on CSF and interstitial fluid (ISF) tracer transport, five groups re-examined the importance of AQP4 in glymphatic transport. We concur that CSF influx is higher in wild-type mice than in four different Aqp4 KO lines and in one line that lacks perivascular AQP4 (Snta1 KO). Meta-analysis of all studies demonstrated a significant decrease in tracer transport in KO mice and rats compared to controls. Meta-regression indicated that anesthesia, age, and tracer delivery explain the opposing results. We also report that intrastriatal injections suppress glymphatic function. This validates the role of AQP4 and shows that glymphatic studies must avoid the use of invasive procedures.
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| 6. |
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| 7. |
- Prasanna, A. P.S., et al.
(författare)
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Multifunctional ZnO/SiO2 Core/Shell Nanoparticles for Bioimaging and Drug Delivery Application
- 2020
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Ingår i: Journal of Fluorescence. - : Springer Science and Business Media LLC. - 1573-4994 .- 1053-0509. ; 30:5, s. 1075-1083
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Tidskriftsartikel (refereegranskat)abstract
- Semiconducting nanoparticles with luminescent properties are used as detection probes and drug carriers in in-vitro and in-vivo analysis. ZnO nanoparticles, due to its biocompatibility and low cost, have shown potential application in bioimaging and drug delivery. Thus, ZnO/SiO2 core/shell nanoparticle was synthesised by wet chemical method for fluorescent probing and drug delivery application. The synthesised core/shell nanomaterial was characterized using XRD, FTIR, UV-VIS spectroscopy, Raman spectroscopy, TEM and PL analysis. The silicon shell enhances the photoluminescence and aqueous stability of the pure ZnO nanoparticles. The porous surface of the shell acts as a carrier for sustained release of curcumin. The synthesized core/shell particle shows high cell viability, hemocompatibility and promising florescent property. [Figure not available: see fulltext.].
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