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Design and preparation of persistently luminescent nanostructured phosphors are of a significant interest in lighting, photonic, and photovoltaic technologies. However, afterglow generally occurs i...

Expanding the range of available aliovalently doped semiconductor nanocrystals has largely been motivated by the potential for realizing and controlling plasmon-exciton coupling in a single phase. ...

Dynamic manipulation of discrete states in nanostructured materials is critical for emerging quantum technologies. However, this process often requires a correlation of mutually competing degrees o...

Degenerately doped metal oxide nanocrystals have emerged as infrared plasmonic materials with promising applications in optoelectronics, surface-enhanced infrared spectroscopies, and sensing. They also have potential for technological applications in electronics and photonics owing to the possibility of coupling between plasmon and exciton in the absence of a heterojunction. Here, we demonstrate the control of excitonic splitting in In2O3 nanocrystals upon excitation with circularly polarized light in an external magnetic field by simultaneous control of the electronic structure of donor defects and the nanocrystal host lattice. Using variable-temperature–variable-field magnetic circular dichroism spectroscopy, we show that the nanocrystal band splitting has two distinct contributions in plasmonic In2O3 nanocrystals. Temperature-independent splitting arises from the cyclotron magnetoplasmonic modes, which impart angular momentum to the conduction band excited states near the Fermi level, and increases wit...

We investigated photocatalytic activity of γ-Ga2O3 nanocrystals with varying compositions. Substitutional doping with In3+ and Zn2+ allows for a control of charge carrier trapping in native defect states, which was studied by time-resolved photoluminescence spectroscopy. Doping nanocrystals with In3+ decreases while doping with Zn2+ increases the lifetime of the carriers trapped on donor and acceptor sites. The apparent rate constant for the photocatalytic dye degradation correlates well with the average donor-acceptor recombination lifetime, suggesting critical importance of carrier trapping for charge separation. The results of this work demonstrate the design of single-phase photocatalysts by controlling carrier trapping via compositional manipulation.

We developed a comprehensive theoretical model describing the photoluminescence decay dynamics at short and long time scales based on the donor-acceptor defect interactions in γ-Ga 2 O 3 nanocrystals, and quantitatively determined the importance of exclusion distance and spatial distribution of defects. We allowed for donors and acceptors to be adjacent to each other or separated by different exclusion distances. The optimal exclusion distance was found to be comparable to the donor Bohr radius and have a strong effect on the photoluminescence decay curve at short times. The importance of the exclusion distance at short time scales was confirmed by Monte Carlo simulations.

Semiconductor photocatalysis has emerged as an efficient and sustainable advanced oxidation process for wastewater treatment and other environmental remediation and forms the basis for water splitting and solar-to-fuel conversion. Nanocrystalline metal oxides are particularly promising photocatalysts because of their efficiency, stability, and low toxicity. However, the influence of the crystal structure and defects on the photocatalytic activity of these polymorphic materials is still poorly understood. In this work we investigated the structural dependence of the photocatalytic activity of nanocrystalline Ga2O3. We demonstrate that metastable cubic-phase γ-Ga2O3 prepared from colloidal nanocrystals exhibits an anomalously high photocatalytic activity, which rapidly decreases upon thermally induced transformation to monoclinic β-Ga2O3. Using steady-state and time-resolved photoluminescence measurements we showed that the reduction in photocatalytic activity upon annealing is accompanied by a decrease in ...

Investigation of the origin of high-Curie temperature ferromagnetism in diluted magnetic oxides has become one of the focal points of research on solid-state magnetism. While several possible mechanisms have been proposed theoretically, broader experimental evidence is still lacking. Here we report a comparative study of the electronic structure and magnetic properties of colloidal Fe-doped In2O3 and SnO2 nanocrystals, as building blocks for grain-boundary-rich diluted magnetic oxide films. The dopant ions in both nanocrystal host lattices are principally in 3+ oxidation state, with possibly a minor presence of Fe2+ in In2O3, and no conclusive evidence of the presence of Fe2+ in SnO2 nanocrystals. Subsequently, we found that Fe-doped In2O3 nanocrystalline films exhibit only minor ferromagnetic ordering (with a magnetic moment of less than ca. 0.1 μB/Fe) and decreasing saturation magnetization with increasing doping concentration at room temperature. The saturation magnetic moment of Fe-doped SnO2 nanocrys...

Development of inorganic phosphors capable of generating white light in a homogeneous and reproducible fashion without the use of rare earth elements can lead to an efficient, long-lasting, and sustainable solid state lighting. The design of such phosphors requires that different inorganic components emitting in complementary spectral ranges are electronically coupled to avoid the challenges associated with a multicomponent approach, such as inhomogeneity, poor chromaticity control, and low color rendering index. Here we demonstrate coupling between electronically excited blue-emitting Ga2O3 and orange-red-emitting CdSe/CdS core/shell nanocrystals by surface-enabled Forster resonance energy transfer. This energy transfer process is evident from quenching of Ga2O3 (donor) and an enhancement of CdSe/CdS (acceptor) nanocrystal emission and is further confirmed through the diminished lifetime of Ga2O3 and significantly extended lifetime of CdSe/CdS nanocrystals in the composite films. Controlling the energy t...

Introducing multiple luminescent centers into colloidal nanocrystals is an attractive way to impart new optical properties into this class of materials. Doping disparate ions into specific nanocrystals is often challenging, due to the preferential incorporation of one type of dopant. Here, we demonstrate the coexistence of europium dopants as divalent and trivalent ions in colloidal Ga2O3 nanocrystals, achieved by controlled in situ reduction of Eu3+ to Eu2+. The two dopant species exhibit distinctly different steady-state and time-resolved photoluminescence, and their ratio can be modified via doping concentration, reaction temperature, or thermal treatment of as-synthesized NCs. The Eu2+ ions are proposed to be stabilized internally owing to the attractive interaction with oxygen vacancies, while Eu3+ dopants partly reside in the nanocrystal surface region. The relationship between the electronic structure of the native defects and the dopant centers is discussed in the context of the overall emission p...

We report a quantitative analysis and development of hybrid white-light-emitting nanoconjugates, prepared by functionalizing colloidal γ-Ga2O3 nanocrystals with selected organic fluorophores. Using the Forster resonance energy transfer (FRET) formalism, we studied the coupling of native defect states in Ga2O3 nanocrystals, as energy donors, with different orange-red-emitting fluorophores bound to nanocrystal surfaces, as energy acceptors. Variations in the average nanocrystal size and dye surface coverage were used to characterize the efficiency of the energy transfer process and the corresponding donor–acceptor separations. The results show that for approximately three rhodamine B molecules per nanocrystal the energy transfer efficiency increases from 23% to 49% by decreasing the NC size from 5.3 to 3.6 nm. These FRET efficiencies correspond to the estimated donor–acceptor distances of 3.55 ± 0.02 and 2.99 ± 0.03 nm, respectively. Similar trends were observed for ATTO 590-conjugated Ga2O3 nanocrystals, a...

Developing new ways of generating white light is of paramount importance for the design of the next generation of smart, energy-efficient lighting sources. Here we report tunable white light emission of hybrid organic–inorganic nanostructures based on colloidal ZnO nanocrystals conjugated with organic fluorophores. These materials act as single nanophosphors owing to the distance-dependent energy transfer between the two components. The defect-based size-tunable ZnO nanocrystal blue-green emission coupled with complementary color emission from different fluorophores allows for the generation of white light with targeted chromaticity, color temperature, and color rendering index. We further show that silane layer-protected nanoconjugates result in increased stability of white light emission over a long period of time. The results of this work demonstrate an inexpensive, green, and sustainable approach to general solid-state lighting, without the use of rare earth or heavy metals. Colloidal form of the repo...

Controlling the crystal structure of transparent metal oxides is essential for tailoring the properties of these polymorphic materials to specific applications. The structural control is usually done via solid state phase transformation at high temperature or pressure. Here, we report the kinetic study of in situ phase transformation of In2O3 nanocrystals from metastable rhombohedral phase to stable cubic phase during their colloidal synthesis. By examining the phase content as a function of time using the model fitting approach, we identified two distinct coexisting mechanisms, surface and interface nucleation. It is shown that the mechanism of phase transformation can be controlled systematically through modulation of temperature and precursor to solvent ratio. The increase in both of these parameters leads to gradual change from surface to interface nucleation, which is associated with the increased probability of nanocrystal contact formation in the solution phase. The activation energy for surface nucleation is found to be 144 ± 30 kJ/mol, very similar to that for interface nucleation. Despite the comparable activation energy, interface nucleation dominates at higher temperatures due to increased nanocrystal interactions. The results of this work demonstrate enhanced control over polymorphic nanocrystal systems and contribute to further understanding of the kinetic processes at the nanoscale, including nucleation, crystallization, and biomineralization.

We report the synthesis and study of the photoluminescence properties of colloidal lanthanide(III)-doped Ga2O3 nanocrystals. The Ga2O3 nanocrystal host lattice acts as a sensitizer of the Eu3+ dopant red emission arising from intra-4f orbital transitions, and concurrently exhibits a strong blue photoluminescence originating from defect-based donor–acceptor pair (DAP) recombination. The Eu3+ sensitization, enabled by the energy transfer from the nanocrystal host lattice to the dopant centers, allows for the generation of dual blue-red emission. Increasing doping concentration leads to a decrease in the donor activation energy allowing for simultaneous control of the optical and electrical properties of these multifunctional nanocrystals. Analyses of the steady-state and time-resolved photoluminescence spectra suggest that Eu3+ ions occupy at least two different sites, which were tentatively designated as the six-coordinate internal and surface-related dopants. Uniquely, both DAP and Eu3+ emissions have long lifetimes (in milliseconds), although Eu3+ luminescence has a slower decay rate. These phenomena enable a temporal modulation of the dual emission and photoluminescence chromaticity on the millisecond timescale. The generality of these findings was demonstrated by preparing Tb3+-doped Ga2O3 nanocrystals, as a blue-green dual emitter. Owing to their optical transparency, electrical properties, emission color versatility, robustness, and fabricability, colloidal lanthanide(III)-doped Ga2O3 nanocrystals are a promising class of multifunctional materials and complex phosphors.

The effect of the host lattice structure on the spectroscopic and magnetic properties of Cr3+-doped In2O3 nanocrystals is reported. The influence of the dopant ions on the nanocrystal growth allows for the solution-phase stabilization and separation of doped colloidal In2O3 nanocrystals having different crystal structures – stable cubic phase (bcc-In2O3) and metastable rhombohedral (rh-In2O3) phase – and comparative study of the electronic structure and magnetic properties of Cr3+ in both polymorphs. Investigations by a range of complementary spectroscopic techniques, including Raman, X-ray absorption and magnetic circular dichroism spectroscopies, revealed that the change in the In2O3 phase leads to distinctly different electronic structure of Cr3+ dopants, associated with a different nature of the substitutional doping sites and different electronic structure of the nanocrystal host lattice. Nanocrystalline films prepared from colloidal nanocrystals exhibit ferromagnetism at room temperature, although t...

We demonstrate the coexistence of Eu(2+) and Eu(3+) in corundum and bixbyite-type colloidal In2O3 nanocrystals. The emission properties of dopants in both oxidation states are determined by their interaction with native defects, and are dramatically different in the two nanocrystal phases. This difference arises from the smaller nanocrystal size and higher defect density in metastable corundum-type nanocrystals.

Developing solid state materials capable of generating homogeneous white light in an energy efficient and resource-sustainable way is central to the design of new and improved devices for various lighting applications. Most currently-used phosphors depend on strategically important rare earth elements, and rely on a multicomponent approach, which produces sub-optimal quality white light. Here, we report the design and preparation of a colloidal white-light emitting nanocrystal conjugate. This conjugate is obtained by linking colloidal Ga2O3 and II–VI nanocrystals in the solution phase with a short bifunctional organic molecule (thioglycolic acid). The two types of nanocrystals are electronically coupled by Förster resonance energy transfer owing to the short separation between Ga2O3 (energy donor) and core/shell CdSe/CdS (energy acceptor) nanocrystals, and the spectral overlap between the photoluminescence of the donor and the absorption of the acceptor. Using steady state and time-resolved photoluminescence spectroscopies, we quantified the contribution of the energy transfer to the photoluminescence spectral power distribution and the corresponding chromaticity of this nanocrystal conjugate. Quantitative understanding of this new system allows for tuning of the emission color and the design of quasi-single white light emitting inorganic phosphors without the use of rare-earth elements.

Understanding the mechanisms of defect-related photoluminescence in colloidal transparent conducting oxide nanocrystals is important for the development of new multifunctional nanostructures and devices. Here we report a study of the role of NC size, structure, defects, and surface capping on the photoluminescence energy, efficiency, and dynamics of colloidal γ-Ga2O3 nanocrystals. A strong blue emission (quantum yield ∼25%) is associated with the presence of the vacancy-defect sites, and assigned to the donor–acceptor pair (DAP) recombination. The emission energy and lifetime are generally determined by the donor and acceptor binding energies (which are dependent on the NC structure) and the attractive Coulombic interactions between charged donor and acceptor sites (which are dependent on the defect concentration). Variable temperature photoluminescence measurements reveal that binding energies of the donor and acceptor levels are also size-dependent; in 6.0 ± 1.0 nm γ-Ga2O3 nanocrystals donor binding ene...

We report the synthesis and separation of colloidal indium tin oxide (ITO) nanocrystals in the stable cubic bixbyite (bcc-ITO) and metastable corundum (rh-ITO) phase under identical conditions, based on the size−structure correlation. Both phases are obtained in the same reactions, with nanocrystals below ca. 5 nm in size having corundum crystal structure. This bimodal size distribution allows for the separation of the nanocrystal phases by size selective precipitation. A comparative study of bcc-ITO and rh-ITO nanocrystals reveals a dramatic difference in their optical and electrical properties. Unlike smaller rh-ITO nanocrystals, bcc-ITO nanocrystals exhibit a strong absorption in the near-infrared (NIR) region arising from the plasmon oscillations due to the presence of free electrons. The difference in the free electron concentration in bcc-ITO and rh-ITO nanocrystals is related to the different electronic structure of the donor states, associated with Sn4+ dopants, in these two nanocrystal allotropic...

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 ...

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....

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.

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.

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 nanocrystal’s 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.

Carbon-Li4Ti5O12 (C-LTO) and carbon nanotube-Li4Ti5O12 (CNT-LTO) nanocomposite particles have been synthesized by hydrothermal method and a following high-temperature calcinations using a mixture of micro-size Li-Ti-O precursors and conducting black and carbon nanotubes, respectively. Two different types of coating layers have been characterized and analyzed on two kinds of Li4Ti5O12 particles surface by high resolution transmission electron microscopy images (HR-TEM) and selected area electron diffraction (SAED). Typical HR-TEM images and SAED patterns at nano-scale confirmed and showed that both particles exhibited a well-developed spinel nanocrystal with average sizes around 20-50 nm. The C-LTO particles exhibited the roughly spherical shape with more than 5 nm graphitic coating uniformly on the spherical surfaces; however, the CNT-LTO particles showed uniform square nanocrystal with edge length around 30 nm and a few layers of graphene covering the surface.Electrochemical studies of galvanostatic discharge/charge cycling capacity testing indicated that both Li4Ti5O12particles showed the superior initial discharge capacity of more than 200 mA·h/g at 0.1C rate, and also the CNT-LTO particles show much improved specific capacity than that of the C-LTO particles during different cycling processing. It has been proposed that, grephene covering layers and the CNT interconnection networks are prove to increase electronic conductivity and improve the kinetics of Li4Ti5O12 toward fast lithium insertion/extraction. The comparative experimental results demonstrated that both nanoscale grephene layer and CNT inter-networks among particles is highly effective in improving the electrochemical properties of the CNT-LTO particles.

We demonstrate redox control of defect-based photoluminescence efficiency of colloidal γ-Ga(2)O(3) nanocrystals. Reducing environment leads to an increase in photoluminescence intensity by enhancing the concentration of oxygen vacancies, while the blue emission is suppressed in oxidative conditions. These results enable optimization of nanocrystal properties by in situ defect manipulation.

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.

The synthesis of colloidal Cr 3+ -doped In 2 O 3 NCs with the body-centered cubic bixbyte-type crystal structure, and Cr 3+ -doped SnO 2 NCs with the rutile crystal structure was described. Ligand-field electronic absorption spectroscopy suggests that Cr 3+ dopants have quasi-octahedral coordination in both In 2 O 3 and SnO 2 NC host lattices. Unlike free-standing nanocrystals, the nanocrystalline films fabricated from colloidal Cr 3+ -doped In 2 O 3 and SnO 2 nanocrystals exhibit room temperature ferromagnetism. Analogous magnetic behavior suggests the same origin of ferromagnetic ordering in both materials. The observed ferromagnetism has been related to the existence of extended structural defects, formed at the interfaces between nanocrystals in nanocrystalline films. These structural defects are likely responsible for the formation of charge carriers which mediate the dopant magnetic moment ordering.

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.

This paper reports the application of ligand-field electronic absorption spectroscopy to probe Co(2+) dopant ions in diluted magnetic semiconductor quantum dots. It is found that standard inverted micelle coprecipitation methods for preparing Co(2+)-doped CdS (Co(2+):CdS) quantum dots yield dopant ions predominantly bound to the nanocrystal surfaces. These Co(2+):CdS nanocrystals are unstable with respect to solvation of surface-bound Co(2+), and time-dependent absorption measurements allow identification of two transient surface-bound intermediates involving solvent-cobalt coordination. Comparison with Co(2+):ZnS quantum dots prepared by the same methods, which show nearly isotropic dopant distribution, indicates that the large mismatch between the ionic radii of Co(2+) (0.74 A) and Cd(2+) (0.97 A) is responsible for exclusion of Co(2+) ions during CdS nanocrystal growth. An isocrystalline core/shell preparative method is developed that allows synthesis of internally doped Co(2+):CdS quantum dots through encapsulation of surface-bound ions beneath additional layers of CdS.

The synthesis of colloidal Cr(3+)-doped SnO(2) nanocrystals prepared under mild conditions via a hydrolysis method is described. We show by means of nanocrystal surface ligand exchange that even under mild reaction conditions a significant fraction of the dopant ions reside on the nanocrystal surfaces. Two different approaches aimed at achieving internal dopant incorporation-surface-bound dopant complexation and isocrystalline shell growth-are described and compared. While free-standing nanocrystals are paramagnetic, the films prepared from the same nanocrystals exhibit ferromagnetic ordering at room temperature. The measured magnetization is associated with structural defects formed at the interfaces of nanocrystals in their films, and discussed in terms of the defect-related itinerant-electron-mediated mechanism. The observed ferromagnetism is compared to ferromagnetism in Cr(3+)-doped In(2)O(3) nanocrystalline films. These results demonstrate the possibility of controlling surface structure and composition of doped oxide nanocrystals using different approaches. Furthermore, this work emphasizes the importance of surface structure and composition in tailoring properties of doped multifunctional transparent conducting oxide nanostructures.

Methods for introducing new magnetic, optical, electronic, photophysical, or photochemical properties to semiconductor nanocrystals are attracting intense applications-oriented interest. In this communication, we report the preparation and electronic absorption spectroscopy of colloidal ZnO DMS-QDs. Our synthetic procedure involves modification of literature methods known to yield highly crystalline and relatively monodisperse nanocrystals of pure ZnO to allow introduction of transition-metal dopants. We use ligand-field electronic absorption spectroscopy as a dopant-specific optical probe to monitor dopant incorporation during nanocrystal growth and to verify internal substitutional doping in Co2+:ZnO and Ni2+:ZnO DMS-QDs. To the best of our knowledge, these are the first free-standing oxide DMS-QDs reported. The synthesis of colloidal oxide DMS-QDs introduces a new category of magnetic semiconductor materials available for detailed physical study and application in nanotechnology.

This paper reports the application of ligand-field electronic absorption spectroscopy to probe Co(2+) dopant ions in diluted magnetic semiconductor quantum dots. It is found that standard inverted micelle coprecipitation methods for preparing Co(2+)-doped CdS (Co(2+):CdS) quantum dots yield dopant ions predominantly bound to the nanocrystal surfaces. These Co(2+):CdS nanocrystals are unstable with respect to solvation of surface-bound Co(2+), and time-dependent absorption measurements allow identification of two transient surface-bound intermediates involving solvent-cobalt coordination. Comparison with Co(2+):ZnS quantum dots prepared by the same methods, which show nearly isotropic dopant distribution, indicates that the large mismatch between the ionic radii of Co(2+) (0.74 A) and Cd(2+) (0.97 A) is responsible for exclusion of Co(2+) ions during CdS nanocrystal growth. An isocrystalline core/shell preparative method is developed that allows synthesis of internally doped Co(2+):CdS quantum dots through encapsulation of surface-bound ions beneath additional layers of CdS.

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.