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We investigated the formation of extended defects in CaFeO2.5, predominantly appearing as antiphase boundaries (APBs), as a function of the synthesis method and temperature. While CaFeO2.5 is known to adopt an ordered oxygen defect structure showing long range order of the (FeO4)∞ chains in its bulk form, interestingly, we demonstrated that the length of these (FeO4)∞ chains can be considerably scaled down to few nanometers by adopting a modified sol-gel method (low temperature synthesis) while the grain size of the resulting nano-phase CaFeO2.5 is around 50 nm. We discuss the synthesis dependent modulation of the length of APBs, characterized by X-ray diffraction and high resolution TEM, to be at the origin of an amplified switching dynamics of the (FeO4)∞ chains. This can accordingly explain the reduction of the onset temperature for oxygen diffusion to set in from 450 °C for bulk-CaFeO2.5 to 320 °C for nano-CaFeO2.5, as determined by 18O/16O oxygen isotope exchange reactions. [ABSTRACT FROM AUTHOR]

We investigated the formation of extended defects in CaFeO2.5, predominantly appearing as antiphase boundaries (APBs), as a function of the synthesis method and temperature. While CaFeO2.5 is known to adopt an ordered oxygen defect structure showing long range order of the (FeO4)∞ chains in its bulk form, interestingly, we demonstrated that the length of these (FeO4)∞ chains can be considerably scaled down to few nanometers by adopting a modified sol-gel method (low temperature synthesis) while the grain size of the resulting nano-phase CaFeO2.5 is around 50 nm. We discuss the synthesis dependent modulation of the length of APBs, characterized by X-ray diffraction and high resolution TEM, to be at the origin of an amplified switching dynamics of the (FeO4)∞ chains. This can accordingly explain the reduction of the onset temperature for oxygen diffusion to set in from 450 °C for bulk-CaFeO2.5 to 320 °C for nano-CaFeO2.5, as determined by 18O/16O oxygen isotope exchange reactions. [ABSTRACT FROM AUTHOR]

We report the growth and low-temperature photoluminescent characteristics of well-aligned Ni-doped ZnO nanoneedles and V-doped ZnO nanostructured thin film grown by a modified pulsed laser deposition technique. Low-temperature photoluminescence spectra of the as-grown films show the presence of free excitonic as well as bound excitonic transitions, whose relative intensity changes with increasing temperature. Ni-doped ZnO films show a characteristic fine structure in the visible range (2.6-2.9 meV) attributed to either exciton-polariton longitudinal-transverse splitting or the splitting caused by electron-hole exchange interaction. The excitonic and visible region emission can be clearly seen as can the phonon replicas produced from longitudinal optical phonons. Different possible attributions of the various peaks in the emission band at low temperature have been discussed. The as-grown nanostructures of Ni- and V-doped ZnO thin films also clearly show the effect of doping on the microstructure of ZnO. [ABSTRACT FROM AUTHOR]

ZnO forks, brooms and spheres possessing self assembled nanowalls and nanocones of ZnO were synthesized, for the first time, via direct thermal evaporation of metallic Zn flakes. The samples exhibit visible green emission on UV excitation. EDX point towards oxygen deficient sample. Photoluminescence studies confirm the presence of defect related emission. The sharp nanocone tips and high degree of networking of nanowalls make them a potential candidate for field emission, gas sensing and catalytic applications. [Copyright &y& Elsevier]

In this paper we report on the preparation of nanobrushes of ZnO on quartz substrate by a direct atmosphere evaporation method using Zn metal flakes. Activated charcoal was used as a catalyst that facilitated the formation of nanobrushes in which the brush stem was about 15–20 μm in length and the bristles (100–200 nm thick) were made up of nanofibrous ZnO whose tips were 10–15 nm in width and were angled in some cases. These aligned nanobrushes can find potential applications as nanopower generators and high aspect ratio AFM probes by virtue of the piezoelectric property of ZnO. This technique is simple for realizing aligned ZnO nanobrushes with metallic Zn as the source material. [ABSTRACT FROM AUTHOR]

Photocatalysis requires light absorption as well as efficient extraction of the photogenerated electron–hole pairs to chemically active sites. To avoid electron–hole recombination, we need tailored nanostructures which can demonstrate novel light absorption and thermodynamic properties. This work shows that band gap modification/narrowing due to the formation of solid solution along with an increased surface area of the nanostructures are ideal for solar harvesting and is a self sufficient photocatalytic agent even in absence of a co-catalyst. The present study suggests that the rate of H 2 production for GaN was negligible and it increased to 32.43 μmol/g/h for the solid solution under visible light irradiation (>400 nm) even in the absence of a co-catalyst. The apparent quantum yield (AQY) efficiency of H 2 evolution was found to be 0.8%. This highly desirable increased H 2 generation activity is attributed to the additional linewidth broadening in the photoluminescence spectra of nanostructured wurtzite Ga 1−x Zn x O 1−z N z solid-solution due to Ga/Zn and N/O interdiffusion giving rise to a modified bandgap and N2p-O2p interaction in the lattice. These inferences are also corroborated by diffuse reflectance spectra of the samples. For the first time, origin of hitherto unreported weak features appearing in the low energy Raman spectrum is also discussed. A series of characterization tools including structural, microstructural, optical, spectroscopic and Photocatalytic hydrogen production studies were employed to support our claim. [ABSTRACT FROM AUTHOR]