Pavle V. Radovanovic

Size-Tunable Phosphorescence in Colloidal Metastable γ-Ga2O3 Nanocrystals

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.

Advances in spinel Li4Ti5O12 anode materials for lithium-ion batteries

Anode materials of rechargeable lithium-ion batteries have been developed towards the aim of high power density, long cycle life, and environmental benignity. As a promising anode material for high power density batteries for large scale applications in both electric vehicle and large stationary power supplies, the spinel Li4Ti5O12 anode has become more attractive for alternative anodes for its relatively high theoretical capacity (175 mA h g−1), stable voltage plateau of 1.5 V vs. Li/Li+, better cycling performance, high safety, easy fabrication, and low cost precursors. This perspective first introduces recent studies on the electronic structure and performance, synthesis methods, and strategies for improvement including carbon-coating, ion-doping, surface modifications, nano-structuring and optimization of the particle morphology of the Li4Ti5O12 anode. Furthermore, practical applications of the commercial spinel lithium-ion batteries are demonstrated. Finally, the future research directions and key developments of the spinel Li4Ti5O12 anode are pointed out from a scientific and an industrial point of view. In addition, the prospect of the synthesis of graphene–Li4Ti5O12 hybrid composite anode materials for next-generation lithium-ion batteries is highlighted.

Colloidal Gallium Indium Oxide Nanocrystals: A Multifunctional Light-Emitting Phosphor Broadly Tunable by Alloy Composition

We demonstrate compositionally tunable photoluminescence in complex transparent conducting oxide nanocrystals. Alloyed gallium indium oxide (GIO) nanocrystals with variable crystal structures are prepared by a colloidal method throughout the full composition range and studied by different structural and spectroscopic methods, including photoluminescence and X-ray absorption. The structures and sizes of the GIO nanocrystals can be simultaneously controlled, owing to the difference in the growth kinetics of In(2)O(3) and Ga(2)O(3) nanocrystals and the polymorphic nature of both materials. Using the synthesized nanocrystal series, we demonstrate the structural and compositional dependences of the photoluminescence of GIO nanocrystals. These dependences, induced by the interactions between specific defect sites acting as electron donors and acceptors, are used to achieve broad emission tunability in the visible spectral range at room temperature. The nature of the photoluminescence is identified as donor-acceptor pair recombination and changes with increasing indium content owing to the changes in the energy states of, and interactions between, donors and acceptors. Structural analysis of GIO nanocrystals by extended X-ray absorption fine structure spectroscopy reveals that In(3+) occupies only octahedral, rather than tetrahedral, sites in the spinel-type γ-Ga(2)O(3) nanocrystal host lattice, until reaching the substitutional incorporation limit of ca. 25%. The emission decay dynamics is also strongly influenced by the nanocrystal structure and composition. The oxygen vacancy defects, responsible for the observed photoluminescence properties, are also implicated in other functional properties, particularly conductivity, enabling the application of colloidal GIO nanocrystals as integrated optoelectronic materials.

Generating Tunable White Light by Resonance Energy Transfer in Transparent Dye-Conjugated Metal Oxide Nanocrystals

We report the design and properties of hybrid white-light-emitting nanophosphors obtained by electronic coupling of defect states in colloidal Ga2O3 nanocrystals emitting in blue-green with selected organic molecules emitting in orange-red. Coupling between the two components is enabled by the nanocrystals size-dependent resonance energy transfer, allowing the photoluminescence chromaticity to be precisely tuned by changing the nanocrystal size and selecting the complementary organic dye molecule. Using this approach, we demonstrate the generation of pure white light with quantum yield of ~30%, color rendering index up to 95, and color temperature of 5500 K. These results provide a guideline for the design of a new class of hybrid white-light-emitting nanophosphors and other multifunctional nanostructures based on transparent metal oxides.

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

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 Cr(3+)-doped BaTiO(3) 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 of the tetragonal phase. A combination of magnetic and magneto-optical measurements revealed that nanocrystalline films prepared from as-synthesized paramagnetic Cr(3+)-doped BaTiO(3) nanocrystals exhibit robust ferromagnetic ordering (up to ca. 2 μ(B)/Cr(3+)), similarly to magnetically doped transparent conducting oxides. The observed ferromagnetism increases with decreasing constituent nanocrystal size because of an enhancement in the interfacial defect concentration with increasing surface-to-volume ratio. Element-specific XMCD spectra measured by scanning transmission X-ray microscopy (STXM) confirmed with high spatial resolution that magnetic ordering arises from Cr(3+) dopant exchange interactions. The results of this work suggest an approach to the design and preparation of multiferroic perovskite materials that retain the ferroelectric phase and exhibit long-range magnetic ordering by using doped colloidal nanocrystals with optimized composition and size as functional building blocks.

General Control of Transition-Metal-Doped GaN Nanowire Growth : Toward Understanding the Mechanism of Dopant Incorporation

We report the first synthesis and characterization of cobalt- and chromium-doped GaN nanowires (NWs), and compare them to manganese-doped GaN NWs. Samples were synthesized by chemical vapor deposition method, using cobalt(II) chloride and chromium(III) chloride as dopant precursors. For all three impurity dopants hexagonal, triangular, and rectangular NWs were observed. The fraction of NWs having a particular morphology depends on the initial concentration of the dopant precursors. While all three dopant ions have the identical effect on GaN NW growth and faceting, Co and Cr are incorporated at much lower concentrations than Mn. These findings suggest that the doping mechanism involves binding of the transition-metal intermediates to specific NW facets, inhibiting their growth and causing a change in the NW morphology. We discuss the doping concentrations of Mn, Co, and Cr in terms of differences in their crystal-field stabilization energies (DeltaCFSE) in their gas-phase intermediates and in substitutionally doped GaN NWs. Using iron(III) chloride and cobalt(II) acetate as dopant precursors we show that the doping concentration dependence on DeltaCFSE allows for the prediction of achievable doping concentrations for different dopant ions in GaN NWs, and for a rational choice of a suitable dopant-ion precursor. This work further demonstrates a general and rational control of GaN NW growth using transition-metal impurities.

Phase Transformation of Colloidal In2O3 Nanocrystals Driven by the Interface Nucleation Mechanism: A Kinetic Study

The kinetics of phase transformation of colloidal In(2)O(3) nanocrystals (NCs) during their synthesis in solution was explored by a combination of structural and spectroscopic methods, including X-ray diffraction, transmission electron microscopy, and extended X-ray absorption fine structure spectroscopy. Johnson-Mehl-Avrami-Erofeyev-Kholmogorov (JMAEK) and the interface nucleation models were used to analyze the isothermal kinetic data for the phase transformation of NCs in the temperature range of 210-260 °C. The results show that NCs are initially stabilized in the metastable corundum (rh-In(2)O(3)) phase. The phase transformation occurs via nucleation of cubic bixbyite (bcc-In(2)O(3)) phase at the interface between contacting rh-In(2)O(3) NCs, and propagates rapidly throughout the NC volume. The activation energy of the phase transformation was determined from the Arrhenius expression to be 152 ± 60 kJ/mol. The interface nucleation rate is maximal at the beginning of the phase transformation process, and decreases over the course of the reaction due to a decrease in the concentration of rh-In(2)O(3) NCs in the reaction mixture. In situ high-temperature XRD patterns collected during nonisothermal treatment of In(2)O(3) NCs reveal that phase transformation of smaller NCs occurs at a faster rate and lower temperature, which is associated with their higher packing density and contact formation probability. Because NC surfaces and interfaces play a key role in phase transformation, their control through the synthesis conditions and reaction kinetics is an effective route to manipulate NC structure and properties.

Evidence of charge-transfer ferromagnetism in transparent diluted magnetic oxide nanocrystals: switching the mechanism of magnetic interactions.

We report the experimental evidence of a new form of room-temperature ferromagnetism in high surface area nanocrystalline manganese-doped In2O3, prepared from colloidal nanocrystals as building blocks. The nanocrystal structure (bixbyite or corundum) and assembly were controlled by their size, and the type and concentration of dopant precursors. The existence of substitutional paramagnetic Mn dopant ions in mixed valence states (Mn(2+) and Mn(3+)) was confirmed and quantified by different spectroscopic methods, including X-ray absorption and magnetic circular dichroism. The presence of different oxidation states is the basis of ferromagnetism induced by Stoner splitting of the local density of states associated with extended structural defects, due to charge transfer from the Mn dopants. The extent of this charge transfer can be controlled by the relationship between the electronic structures of the nanocrystal host lattice and dopant ions, rendering a higher magnetic moment in bixbyite relative to corundum Mn-doped In2O3. Charge-transfer ferromagnetism assumes no essential role of dopant as a carrier of the magnetic moment, which was directly confirmed by X-ray magnetic circular dichroism, as an element-specific probe of the origin of ferromagnetism. At doping concentrations approaching the percolation limit, charge-transfer ferromagnetism can switch to a double exchange mechanism, given the mixed oxidation states of Mn dopants. The results of this work enable the investigations of the new mechanisms of magnetic ordering in solid state and contribute to the design of new unconventional magnetic and multifunctional materials.

Origin of size-dependent photoluminescence decay dynamics in colloidal γ-Ga2O3 nanocrystals

We studied size-dependent dynamics of defect-based photoluminescence of colloidal γ-Ga2O3 nanocrystals in the framework of the donor-acceptor pair model. Two theoretical models were developed based on relative positioning of donor and acceptor sites: (1) for random distribution of defects throughout the nanocrystal volume and (2) for surface segregation of defects. The results of the modeling indicate that defect sites are predominantly located in the vicinity of nanocrystal surfaces and that the density of defects increases with decreasing nanocrystal size. The donor Bohr radius obtained as a fitting parameter suggests an increase in the donor binding energy with decreasing nanocrystal size.

Electronic structure and magnetic properties of sub-3 nm diameter Mn-doped SnO2 nanocrystals and nanowires

Manganese-doped SnO2 nanocrystals and nanowires with diameters below SnO2 Bohr radius were synthesized by solution methods. X-ray absorption studies reveal that dopant ions are substitutionally incorporated as Mn2+ and Mn3+. Mn2+ is the dominant species at low doping levels, but the fraction of Mn3+ increases with doping concentration. Room-temperature ferromagnetism with the saturation moment of 0.27 μB/Mn is observed for nanocrystalline films containing high fraction of Mn2+ dopant, which is associated with hybridization of Mn2+ d-levels with a donor-impurity band. These results imply the possibility of manipulating magnetic interactions via dopant electronic structure and quantum confinement of the host lattice.