Search arXivSearch

arXiv · 1109.5973

Affect of film thickness on the blue photoluminescence from ZnO

Abstract

Zinc oxide (ZnO) films having various thicknesses were synthesized on sapphire substrates by thermal oxidation of Zn-metallic films in air ambient. X-ray diffraction (XRD) spectra indicate that the resulting films possess a polycrystalline hexagonal wurtzite structure without preferred orientation. For films having a thickness of 200 nm, crystal grain size was observed to decrease with increasing annealing temperature up to 600C, and then increase at higher temperatures. Thicker films demonstrated a modest increase in grain size as temperature increased from 300C to 1200C. The influence of film thickness on the optical properties was investigated using room temperature photoluminescence (PL). Specifically, PL spectra indicate four emission bands: excitonic ultraviolet, blue, and deep-level green and yellow emission. The strongest UV emission and narrowest full width at half maximum (0.09 eV) was observed for films having a thickness of 200 nm and annealed at low temperature (300C). The ratio of deep-level green emission to UV excitonic emission was observed to decrease with decreasing annealing temperature, which is attributed to the generation of fewer oxygen vacancies and interstitial oxygen ions in the bulk. As film thickness decreased, we observed the emergence of blue emission and a significant red shift (0.15 eV) in the bandgap. The emergence of blue emission and the corresponding decrease in emission associated with bulk defects when depletion width grows relative to the bulk suggests that the origin of the blue emission is related to the negatively charged Zinc interstitials found within the deletion region near the interface.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J. C. Moore, L. R. Covington, R. Stansell. 2011-10-07. Affect of film thickness on the blue photoluminescence from ZnO. https://doi.org/10.1002/pssa.201127613

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Competing effects of Si and Mg doping on native point defects in yttrium aluminum garnet

We investigate how Si and Mg doping affect native point defects in yttrium aluminum garnet (YAG) by combining first-principles calculations with a thermodynamic model of defect equilibria. Formation energies and equilibrium concentrations of native defects, dopants, and defect complexes are obtained across the full range of oxygen chemical potentials relevant to ceramic sintering. Donor (Si) and acceptor (Mg) dopants are found to control native defect populations efficiently but in opposite directions: Si substantially raises cation-vacancy concentrations while suppressing oxygen vacancies, whereas Mg produces the reverse trend. Depending on dopant concentration and oxygen chemical potential, native vacancy concentrations vary by up to thirteen orders of magnitude. The concentration of isolated cation vacancies depends nonmonotonically on Si content, a consequence of Si-vacancy complex formation. Under Si-Mg co-doping, the two dopants compensate each other efficiently, giving rise to pronounced minima in both cation- and oxygen-vacancy concentrations when Si and Mg are present in equal amounts. These findings provide a microscopic basis for the pronounced sensitivity of YAG sintering behavior to the Si/Mg ratio, and show that balanced donor-acceptor co-doping is an effective strategy for controlling native defect populations in YAG.

cond-mat.mtrl-sci

Statistical admissibility and long-wavelength structural convergence determine representative support in granular materials

Representative elementary areas and volumes provide the scale bridge between resolved granular microstructure and continuum-scale material properties, yet they are still commonly selected from the apparent stabilization of a single scalar observable. Such plateaus can be false indicators of representativeness when statistically incompatible regions are averaged together or when long-wavelength structural correlations remain unresolved. We introduce a general representative-support framework for granular materials based on three sequential requirements: statistical admissibility of the sampled domain, persistent convergence of the apparent field mean and the low-wavenumber covariance spectrum, and validation against independent effective properties. The concept is tested on seven large-area backscattered-electron images of Arabian dune sands and mineral-resolved QEMSCAN maps. The structure-only criterion identifies a representative elementary area of $1536$ pixels, corresponding to approximately $2.01~\mathrm{mm}$. Without property-specific fitting or recalibration, the same physical scale transferred to the QEMSCAN grid $(\approx 2.04~\mathrm{mm})$ coincides with the onset of weak size dependence in apparent thermal conductivity, elastic stiffness, and directional Young's moduli. Thus, the representative scale inferred from long-wavelength granular organization independently predicts the convergence of distinct constitutive responses. The results show that representative support should be assigned only after both statistical compatibility and long-range structural convergence have been established. Although demonstrated here on two-dimensional dune-sand sections, the criterion is formulated for granular materials generally and has a direct mathematical extension to three-dimensional voxelized volumes.

cond-mat.mtrl-sci

Interplay of spin-lattice and electronic coupling far above Neel ordering in 2D antiferromagnetic CrPS4 and its interface manifestation

A short-range spin correlation driven, strongly intercoupled spin-phonon-electronic state far above TN (~38K) is identified in the low dimensional van der Waals antiferromagnet CrPS4. Temperature-dependent Raman spectroscopy reveals spin-phonon coupling persisting up to T*~120K, concomitant with local lattice distortion. The setting of vibronic progression in photoluminescence spectra suggests the strengthening of electron-phonon coupling around T*. Furthermore, both the electrical transport and optoelectronic response also change significantly at T*. The results indicate that spin-phonon coupling above TN in CrPS4 originates from local lattice distortion induced by short range magnetic correlations which in turn enhances the electron-phonon interaction. Furthermore, using a CrPS4/In2Se3 heterostructure, we demonstrate that the anomaly associated with the coupled degrees of freedom in CrPS4 also influences the adjacent In2Se3 layer. The lattice dynamics of In2Se3 is significantly modified across the magnetic anomaly of CrPS4, and the coupled dynamics is observed at T*. These interfacial manifestation opens up new possibilities for achieving correlated multifunctionalities in artificially designed heterostructure.

cond-mat.mtrl-sci