Asad Mumtaz

Core–Shell Vanadium Modified Titania@β-In2S3 Hybrid Nanorod Arrays for Superior Interface Stability and Photochemical Activity

Core-shell rutile TiO2@β-In2S3 and modified V-TiO2@β-In2S3 were synthesized to develop bilayer systems to uphold charge transport via an effective and stable interface. Morphological studies revealed that β-In2S3 was deposited homogeneously on V-TiO2 as compared to unmodified TiO2 nanorod arrays. X-ray photoelectron spectroscopy (XPS) and electron energy loss spectrometry studies verified the presence of various oxidation states of vanadium in rutile TiO2 and the vanadium surface was utilized for broadening the charge collection centers in host substrate layer and hole quencher window. Subsequently, X-ray diffraction, high-resolution transmission electron microscopy, and Raman spectra confirmed the rutile phases of TiO2 and modified V-TiO2 along with the phases of crystalline β-In2S3. XPS valence band study explored the interaction of valence band quazi Fermi levels of β-In2S3 with the conduction band quazi Fermi levels of modified V-TiO2 for enhanced charge collection at the interface. Photoelectrochemical studies show that the photocurrent density of V-TiO2@β-In2S3 is 1.42 mA/cm(2) (1.5AM illumination). Also, the frequency window for TiO2 was broadened by the vanadium modification in rutile TiO2 nanorod arrays, and the lifetime of the charge carrier and stability of the interface in V-TiO2@β-In2S3 were enhanced compared to the unmodified TiO2@β-In2S3. These findings highlight the significance of modifications in host substrates and interfaces, which have profound implications on interphase stability, photocatalysis and solar-fuel-based devices.

Influence of the electrodeposition potential on the crystallographic structure and effective magnetic easy axis of cobalt nanowires

Cobalt nanowires (NWs) have been synthesized by electrodeposition inside the pores of anodized aluminium oxide templates, at different values of applied deposition potential. The as-deposited NWs are parallel to one another and exhibit a high geometrical aspect ratio. The crystal structure of these NWs shows a strong dependence on the applied deposition potential during synthesis. X-ray diffraction indicates the predominance of hexagonal-closed-packed (HCP) phase with (002) texture at low applied deposition potentials, whereas a reorientation of the c-axis of the HCP structure is observed for high electrodeposition potentials. Moreover, for a given electrodeposition time, the length of the NWs also increases with the applied potential. As a result of these structural changes, a switch in the magnetic easy axis, from parallel to perpendicular to the NW axis, occurs depending on the applied potential. A simplified model is used to account for this reorientation of the effective magnetic anisotropy direction, which takes into account the interplay between shape anisotropy, magnetocrystalline anisotropy and interwire dipolar interactions.

Investigation of tip sonication effects on structural quality of graphene nanoplatelets (GNPs) for superior solvent dispersion

The exceptional properties of graphene and its structural uniqueness can improve the performance of nanocomposites if it can attain the uniform dispersion. Tip sonication assisted graphene solvent dispersion has been emerged as an efficient approach but it can cause significant degradation of graphene structure. This study aimed to evaluate the parametric influence of tip sonication on the characteristics of sp2 carbon structure in graphene nanoplatelets by varying the sonication time and respective energy at three different amplitudes (60%, 80% and 100%). The study is essential to identify appropriate parameters so as to achieve high-quality and defect-free graphene with a highly desirable aspect ratio after solvent dispersion for composite reinforcement. Quantitative approach via Raman spectroscopy is used to find the defect ratio and lateral size of graphene evolved under the effect of tip sonication parameters. Results imply that the defect ratio is steady and increases continually with GNPs, along with the transformation to the nano-crystalline stage I up to 60 min sonication at all amplitudes. Exfoliation was clearly observed at all amplitudes together with sheet re-stacking due to considerable size reduction of sheets with large quantity. Finally, considerable GNPs fragmentation occurred during sonication with increased amplitude and time as confirmed by the reduction of sp2 domain (La) and flake size. This also validates the formation of edge-type defect in graphene. Convincingly, lower amplitude and time (up to 60 min) produce better results for a low defect content and larger particle size as quantified by Raman analysis.

Nanoporous TiO2 developed from two templates for their use in photovoltaic applications

Described work is a development of templated nanoporous TiO2 using two different substrates. Controlled parametric syntheses of nanoporous textures give rise high surface area as well as high aspect ratios. High electric field application for specific time and the composition of electrolytes used in synthesis cell needs a careful study. Ethylene glycol, an organic solvent, with F- free ions in the presence of HCl is used for the purpose in cell bath. Ti templated and Ti-Al templated nanoporous TiO2 shows lower porosity at low voltage treatments, while both the templates reveal high porous structure at 20V. Increasing the time of Ti template for a specific voltage leads to collapse of pores while it enhances the roughness of the walls of collapsed pores and hence improving the surface rea. Energy dispersive x-ray (EDX) elemental analysis confirms the presence of TiO2.

Surfactant-decorated graphite nanoplatelets (GNPs) reinforced aluminum nanocomposites: sintering effects on hardness and wear

The exceptional properties of graphene make it ideal as a reinforcement to enhance the properties of aluminum matrices and this critically depends on uniform dispersion. In this study, the dispersion issue was addressed by sonication and non-covalent surface functionalization of graphite nanoplatelets (GNPs) using two types of surfactant: anionic (sodium dodecyl benzene sulfate (SDBS)) and non-ionic polymeric (ethyl cellulose (EC)). After colloidal mixing with Al powder, consolidation was performed at two sintering temperatures (550 and 620°C). The structure, density, mechanical and wear properties of the nanocomposite samples were investigated and compared with a pure Al and a pure GNPs/Al nanocomposite sample. Noticeably, EC-based 0.5wt% GNPs/Al samples showed the highest increment of 31% increase in hardness with reduced wear rate of 98.25% at 620°C, while a 22% increase in hardness with reduced wear rate of 96.98% at 550°C was observed, as compared to pure Al. Microstructural analysis and the overall results validate the use of EC-based GNPs/Al nanocomposites as they performed better than pure Al and pure GNPs/Al nanocomposite at both sintering temperatures.

Enhanced photoelectrochemical activity by nanostructured V2O5/TiO2 bilayer

Hydrogen production by splitting of water using solar means is a renewable alternative and is a need of the hour. The generation of hydrogen is studied using nanostructured V2O5/TiO2 bilayer photoctatalyst synthesized by two different methods. The solution deposition followed by annealing and flame oxidized methods are applied to deposit the nanostructured V2O5 onto TiO2 nanorod arrays. These two methods are compared and studied using X-ray diffraction, field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), electron energy loss spectrum and photoelectrochemical study. The morphological study provides the optimized surface area of the TiO2 nanorod arrays. It shows that 0.45 mL tetra butyl titanate at 180C shows the improved surface area. It also differentiates the 3D network as morphology of nanostructured V2O5/TiO2 bilayer photoctatalyst synthesized by flame oxidation method. Electron energy loss spectrum confirms the presence of respective elemental states of V2O5/Ti...

Synergetic effects of II-VI sensitization upon TiO2 for photoelectrochemical water splitting; a tri-layered structured scheme

Worlds energy demands are growing on a higher scale increasing the need of more reliable and long term renewable energy resources. Efficient photo-electrochemical (PEC) devices based on novel nano-structured designs for solar-hydrogen generation need to be developed. This study provides an insight of the tri-layered-TiO2 based nanostructures. Observing the mechanism of hydrogen production, the comparison of the structural order during the synthesis is pronounced. The sequence in the tri-layered structure affects the photogenerated electron (e−) and hole (h+) pair transfer and separation. It is also discussed that not only the semiconductors band gaps alignment is important with respect to the water redox potential but also the interfacial regions. Quasi-Fermi-level adjustment at the interfacial regions plays a key role in deciding the solar to hydrogen efficiency. More efficient multicomponent semiconductor nano-design (MCSN) could be developed with the approach given in this study.