The polarized optical spectra of the ions Ti3+, V3+, Cr3+, Mn3+, Co3+, and Ni3+ in corundum single crystals have been studied at temperatures from 4.2° to 1200°K. A theory of the band strength based on the point‐charge model and p‐d mixing has been developed and applied to the data with results in fair agreement with experiment. The effects of temperature show that the vibrational‐electronic contribution to band strength is quite small at low temperature but may be appreciable at high temperatures. The crystal‐field parameters have been calculated as convergent lattice sums. The observed trigonal‐field parameter has the opposite sign from that calculated by the point‐charge model if the impurity ion is assumed to occupy an Al3+ ion position in the lattice, but has the same sign as calculated for an ion 0.1 A displaced along the c3 axis toward the empty octahedral site. Details of the spectra have been interpreted as showing that the surroundings of an ion are distorted in some electronic states.

Optical spectra of transition-metal ions in corundum

We report a colloidal synthesis of gallium oxide (Ga(2)O(3)) nanocrystals having metastable cubic crystal structure (gamma phase) and uniform size distribution. Using the synthesized nanocrystal size series we demonstrate for the first time a size-tunable photoluminescence in Ga(2)O(3) from ultraviolet to blue, with the emission shifting to lower energies with increasing nanocrystal size. The observed photoluminescence is dominated by defect-based donor-acceptor pair recombination and has a lifetime of several milliseconds. Importantly, the decay of this phosphorescence is also size dependent. The phosphorescence energy and the decay rate increase with decreasing nanocrystal size, owing to a reduced donor-acceptor separation. These results allow for a rational and predictable tuning of the optical properties of this technologically important material and demonstrate the possibility of manipulating the localized defect interactions via nanocrystal size. Furthermore, the same defect states, particularly donors, are also implicated in electrical conductivity rendering monodispersed Ga(2)O(3) nanocrystals a promising material for multifunctional optoelectronic structures and devices.

Size-Tunable Phosphorescence in Colloidal Metastable γ-Ga2O3 Nanocrystals

Doping semiconductor nanocrystals is crucial for enhancing and manipulating their functional properties, but the doping mechanism and the effects of dopants on the nanocrystal growth and structure ...

Dopant-Induced Manipulation of the Growth and Structural Metastability of Colloidal Indium Oxide Nanocrystals

Morphological and phase transformations during the growth of In2O3 nanocrystals are reported. We demonstrate a direct correlation between the nanocrystal size and structure and show that metastable corundum-type In2O3 is a transient structure in the formation of bixbyite-type nanocrystals. Metastable In2O3 can be spontaneously stabilized in nanocrystals below 5 nm.

Phase-Controlled Synthesis of Colloidal In2O3 Nanocrystals via Size-Structure Correlation

Multiferroics, materials that exhibit coupling between spontaneous magnetic and electric dipole ordering, have significant potential for high-density memory storage and the design of complex multistate memory elements. In this work, we have demonstrated the solvent-controlled synthesis of Cr3+-doped BaTiO3 nanocrystals and investigated the effects of size and doping concentration on their structure and phase transformation using X-ray diffraction and Raman spectroscopy. The magnetic properties of these nanocrystals were studied by magnetic susceptibility, magnetic circular dichroism (MCD), and X-ray magnetic circular dichroism (XMCD) measurements. We observed that a decrease in nanocrystal size and an increase in doping concentration favor the stabilization of the paraelectric cubic phase, although the ferroelectric tetragonal phase is partly retained even in ca. 7 nm nanocrystals having the doping concentration of ca. 5%. The chromium(III) doping was determined to be a dominant factor for destabilization...

Interplay between Size, Composition, and Phase Transition of Nanocrystalline Cr3+-Doped BaTiO3 as a Path to Multiferroism in Perovskite-Type Oxides

Colloidal free-standing Cr3+-doped In2O3 nanocrystals were synthesized in oleylamine from indium (III) and chromium (III) acetylacetonate precursors. The nanocrystals were treated with trioctylphosphine oxide to remove surface-bound dopant ions and ensure internal doping. The lattice resolved transmission electron microscopy images reveal that nanocrystals are faceted and highly crystalline, with no evidence of a secondary phase formation. The average doping concentration estimated with energy dispersive X-ray spectroscopy at the single nanocrystal level agrees with the average doping concentration from the analogous nanocrystal ensemble measurement. Ligand-field electronic absorption spectroscopy suggests that Cr3+ dopants are preferentially substituted for In3+ ions in their trigonally distorted octahedral (b) sites in In2O3 nanocrystals. Nanocrystalline films, prepared under mild conditions using colloidal Cr3+-doped In2O3 nanocrystals as building blocks, exhibit robust room temperature ferromagnetism....

Colloidal Chromium-Doped In2O3 Nanocrystals as Building Blocks for High-TC Ferromagnetic Transparent Conducting Oxide Structures

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Colloidal Chromium-Doped In2O3 Nanocrystals as Building Blocks for High-TC Ferromagnetic Transparent Conducting Oxide Structures