Browsing by Subject "Core shell nano structures"
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Item Open Access Amorphous to tetragonal zirconia anostructures and evolution of valence and core regions(American Chemical Society, 2015) Vempati S.; Kayaci-Senirmak, F.; Ozgit-Akgun, C.; Bıyıklı, Necmi; Uyar, TamerIn this report, we study the evolution of valence band (VB) structure during a controlled amorphous to tetragonal transformation of ZrO2 core-shell nanostructures fabricated from electrospun nanofiber template (at 130, 200, and 250 °C). Shell-ZrO2 was formed with atomic layer deposition. X-ray diffraction and transmission electron microscopy are employed to unveil the transformation of amorphous to crystalline structure of ZrO2. O 1s core-level spectra indicated chemisorbed oxygen (OCh) of almost invariant fraction for the three samples. Zr 3s level suggested that the sample deposited at 130 °C has depicted a peak at relatively higher binding energy. Analyses on Zr 3d spectra indicated the presence of metallic-Zr (Zr+ζ, 0 ≤ |ζ| < 4), the fraction of which decreases with increasing template temperature. VB region is analyzed until ∼64 eV below the Fermi level (EF). The region close to EF depicted features that are dissimilar to the literature. This discrepancy is explained on the basis of the analyses from O 1s, Zr 3d, and Zr 4p levels including hybridization of orbitals from chemisorbed species. These levels were analyzed in terms of peak characteristics such as spectral position, area under the peak, etc. The results of this study would enhance the understanding of the evolution of various bands in the presence of OCh and changes to the crystallinity enabling the functionalities that are not available in the single-phase ZrO2.Item Open Access Nanograined surface shell wall controlled ZnO–ZnS core–shell nanofibers and their shell wall thickness dependent visible photocatalytic properties(Royal Society of Chemistry, 2017) Ranjith, K. S.; Senthamizhan A.; Balusamy, B.; Uyar, TamerThe core-shell form of ZnO-ZnS based heterostructural nanofibers (NF) has received increased attention for use as a photocatalyst owing to its potential for outstanding performance under visible irradiation. One viable strategy to realize the efficient separation of photoinduced charge carriers in order to improve catalytic efficiency is to design core-shell nanostructures. But the shell wall thickness plays a vital role in effective carrier separation and lowering the recombination rate. A one dimensional (1D) form of shell wall controlled ZnO-ZnS core-shell nanofibers has been successfully prepared via electrospinning followed by a sulfidation process. The ZnS shell wall thickness can be adjusted from 5 to 50 nm with a variation in the sulfidation reaction time between 30 min and 540 min. The results indicate that the surfaces of the ZnO nanofibers were converted to a ZnS shell layer via the sulfidation process, inducing visible absorption behavior. Photoluminescence (PL) spectral analysis indicated that the introduction of a ZnS shell layer improved electron and hole separation efficiency. A strong correlation between effective charge separation and the shell wall thickness aids the catalytic behavior of the nanofiber network and improves its visible responsive nature. The comparative degradation efficiency toward methylene blue (MB) has been studied and the results showed that the ZnO-ZnS nanofibers with a shell wall thickness of ∼20 nm have 9 times higher efficiency than pristine ZnO nanofibers, which was attributed to effective charge separation and the visible response of the heterostructural nanofibers. In addition, they have been shown to have a strong effect on the degradation of Rhodamine B (Rh B) and 4-nitrophenol (4-NP), with promising reusable catalytic efficiency. The shell layer upgraded the nanofiber by acting as a protective layer, thus avoiding the photo-corrosion of ZnO during the catalytic process. A credible mechanism for the charge transfer process and a mechanism for photocatalysis supported by trapping experiments in the ZnO-ZnS heterostructural system for the degradation of an aqueous solution of MB are also explicated. Trapping experiments indicate that h+ and OH are the main active species in the ZnO-ZnS heterostructural catalyst, which do not effectively contribute in a bare ZnO catalytic system. Our work also highlights the stability and recyclability of the core-shell nanostructure photocatalyst and supports its potential for environmental applications. We thus anticipate that our results show broad potential in the photocatalysis domain for the design of a visible light functional and reusable core-shell nanostructured photocatalyst.