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Geoffrey A Ozin

Publications and source records attributed to Geoffrey A Ozin.

At least 19 recordsLinked to original sources

Fabry-Perot etalons using colloidal photonic crystal mirrors.

Fabry-Perot etalons have been fabricated with 3D colloidal photonic crystal mirrors. The colloid films were optimized for high reflection and low loss to provide good finesse values in the 1200-1700 nm spectral range. A cavity quality factor of 2400 and a finesse of 8 together with sharp 0.5 nm wide resonance transmission peaks are reported that attest to the relatively good optical quality of the three-dimensionally structured films and the promise of self-assembly colloidal crystal chemistry in providing novel microporous optical interferometers for potential applications such as environmental and biological sensing.

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Three-dimensional silicon inverse photonic quasicrystals for infrared wavelengths.

Quasicrystals are a class of lattices characterized by a lack of translational symmetry. Nevertheless, the points of the lattice are deterministically arranged, obeying rotational symmetry. Thus, we expect properties that are different from both crystals and glasses. Indeed, naturally occurring electronic quasicrystals (for example, AlPdMn metal alloys) show peculiar electronic, vibrational and physico-chemical properties. Regarding artificial quasicrystals for electromagnetic waves, three-dimensional (3D) structures have recently been realized at GHz frequencies and 2D structures have been reported for the near-infrared region. Here, we report on the first fabrication and characterization of 3D quasicrystals for infrared frequencies. Using direct laser writing combined with a silicon inversion procedure, we achieve high-quality silicon inverse icosahedral structures. Both polymeric and silicon quasicrystals are characterized by means of electron microscopy and visible-light Laue diffraction. The diffraction patterns of structures with a local five-fold real-space symmetry axis reveal a ten-fold symmetry as required by theory for 3D structures.

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Size-dependent extinction coefficients of PbS quantum dots.

We report here on a detailed study on PbS colloidal quantum dots. A characterization via X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM) allowed us to reliably determine the diameter and the shape of the nanocrystals. These data, together with second-derivative analysis of the absorption spectra, allowed us to determine the size dependence of seven transitions in the absorption spectrum; some of these transitions were identified on the basis of their normalized confinement energy. The size dependence of the first excitonic transition was best modeled by a four-band envelope approach which considers the anisotropy of the band edges (Andreev, A. D.; Lipovskii, A. A. Phys. Rev. B: Condens. Matter Mater. Phys. 1999, 59, 15402-15404). The extinction coefficients were calculated using concentrations obtained from inductively coupled plasma atomic emission spectrometry (ICP-AES), and their size dependence was found to follow a power law with exponent equal to approximately 2.5. In contrast with what was expected from the effective mass approximation, the per particle absorption cross section of the lowest transition was found to be strongly dependent on the particle size.

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Multigram scale, solventless, and diffusion-controlled route to highly monodisperse PbS nanocrystals.

High-quality PbS nanocrystals were produced in multigram-scale quantities through a solventless, heterogeneous, and relatively green route. The heterogeneous nature of this reaction allows one to limit the diffusion in the system, allowing for unprecedented monodispersity and quality of the product demonstrated by a full-width at half-maximum of the photoluminescence peak (PL fwhm) as low as 52 meV, a Stokes shift as low as 10 meV, and a quantum yield (QY) of 40%. The growth of the nanocrystals is interpreted in the framework of a diffusion-controlled Ostwald growth in conditions of strong supersaturation.

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Mesoporous bragg stack color tunable sensors.

Herein we report a novel self-assembly synthesis, structural and optical characterization of mesoporous Bragg stacks (MBS) composed of spin-coated multilayer stacks of mesoporous TiO(2) and mesoporous SiO(2). Investigation of the optical response of MBS to the infiltration of alcohols and alkanes into its pores reveals better sensitivity and selectivity than conventional Bragg reflectors. Furthermore, we demonstrate that the chemical sensing ability can be tuned via layer thickness, composition and surface properties.

Adsorption↗

Block copolymers under periodic, strong three-dimensional confinement.

In this communication we study the influence of strong 3D confinement on the self-assembly of diblock copolymers containing a polyferrocenylsilane metallopolymer segment. Both silica colloidal crystals and silica inverse colloidal crystals, having nanometer-scale interconnected pore networks, are used as molds to direct the self-assembly. Unusual morphologies, such as concentric shells and branched lamellae, result from the interaction of the polymer with the high surface area topologically periodic templates.

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Photochemically and thermally tunable planar defects in colloidal photonic crystals.

We report a bottom-up synthesis of a photochemically and thermally active azobenzene-based polyelectrolyte multilayer (PEM) planar defect embedded in a colloidal photonic crystal (CPC). Both photoisomerization and thermal cycling lead to a precise tuning of an intragap transmitting state induced by the PEM structural defect.

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Tailoring photonic crystals with nanometer-scale precision using polyelectrolyte multilayers.

In this paper, we describe a rapid, accurate, and convenient method for postsynthetically tuning the optical properties of colloidal photonic crystals. High quality photonic crystal films are first synthesized and then coated iteratively with layers of water-soluble polyelectrolytes. The coating process results in nanometer-scale shifts in the photonic stop band, a process which has been monitored by theoretical modeling. The results suggest a fundamentally different, reproducible layering mechanism inside the confined spaces of the colloidal crystal where polyelectrolyte multilayers are less densely packed.

Letter↗

Evolution of nanocrystallinity in periodic mesoporous anatase thin films.

Herein we report the first kinetic study of the intrachannel wall phase-transition of amorphous titania to nanocrystalline anatase for periodic mesoporous titania thin films, monitored by time-resolved in situ high-temperature X-ray diffraction. Structural transformations associated with the phase transition are further probed by high-resolution scanning electron microscopy and transmission electron microscopy. The model found to be most consistent with the kinetic data involves 1D diffusion-controlled growth of nanocrystalline anatase within the spatial confines of the channel walls of the mesostructure. The observation of anisotropic, rod-shaped anatase nanocrystals preferentially aligned along the channel axis implies that the framework of the liquid-crystal-templated mesostructure guides the crystal growth.

Anisotropy↗

Past, present, and future of periodic mesoporous organosilicas-the PMOs.

Periodic mesoporous organosilicas (PMOs) represent an exciting new class of organic-inorganic nanocomposites targeted for a broad range of applications such as catalysis and sensing, separations, and microelectronics. Their hallmark is the presence of organic bridging groups incorporated into the channel walls of an ordered nanoporous structure, which represents a useful tool to finely tune the chemical and physical properties of the materials. We discuss the history of the discovery and development of the PMOs emphasizing the most important recent advancements regarding compositions and structures, morphologies, and properties. Furthermore, we present an outlook about the promising future perspectives of PMOs that result from the latest developments in this field.

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Synthetic self-propelled nanorotors.

Self-powered completely synthetic nanorotors have been prepared from barcoded gold-nickel nanorods having the gold end anchored to the surface of a silicon wafer; constant velocity circular movements are observed when hydrogen peroxide fuel is catalytically decomposed to oxygen at the unattached nickel end of the nanorod.

Electric Power Supplies↗

Periodic mesoporous dendrisilicas.

We report the synthesis of a new class of materials called periodic mesoporous dendrisilicas. They are prepared from dendrimers with trialkoxysilyl groups at the outmost shell. Dendrimers of various cores and numbers of shells are used. The dendrisilica synthesis is based on acid- or base-catalyzed hydrolysis of the trialkoxysilyl groups and subsequent template-directed condensation of the dendrimers into an ordered template-dendrisilica nanocomposite. The template can be removed with organic solvents, producing a periodic mesoporous dendrisilica whose pore walls consist of interconnected dendrimer building blocks.

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Towards flexible inorganic "mesomaterials": one-pot low temperature synthesis of mesostructured nanocrystalline titania.

We hereby report a simple route for the low temperature synthesis of mesoporous nanocrystalline titania involving brief hydrothermal treatment of butanolic precursors and non-ionic tri-block-copolymer surfactant at 100 degrees C, followed by evaporation induced self assembly to make a crack-free flexible film. At no time in the film-forming process is a temperature of more than 120 degrees C reached, thereby permitting the use of substrates that are not stable to higher temperatures.

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Promises and problems of mesoscale materials chemistry or why meso?

Manipulation and control of chemical structures on the mesoscale has recently developed to a very promising and also aesthetically appealing area of chemistry. This concept article tries to integrate the views of two experts to delineate the specific principles, approaches, and the novel opportunities for chemistry that arise from the rational control of matter and functionality on that scale.

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Colloidal crystal films: advances in universality and perfection.

For three-dimensional photonic crystals, made either by top-down microfabrication or by bottom-up self-assembly approaches, to comply with the stringent requirements of optical telecommunication applications, their degree of structural perfection and optical quality must meet an exceptionally high standard. Only with such superior quality photonic crystals can their unique optical properties be harnessed in optical devices and circuits constructed from micrometer-sized optical components. In this paper, we present a new strategy for making silica colloidal crystal films with a sufficiently high level of structural perfection and optical quality to make it competitive as a practical route to photonic crystal optical components. The attainment of this goal takes due cognizance of three key synergistic factors in the film formation process. The first recognizes the necessity to prepare high-quality silica spheres, which are highly monodisperse, with a polydispersity index significantly better than 2%, and the second recognizes that the population of spheres must be devoid of even the smallest fraction of substantially smaller or larger spheres or sphere doublets. The latter turns out to have a minimal effect on the polydispersity index, and yet a major detrimental effect on the overall structural order of the film. The third concerns the film-forming method itself, which necessitated the development of a novel process founded upon isothermal heating evaporation-induced self-assembly (IHEISA) of spheres on a planar substrate. This new method has several advantages over previously reported ones. It is able to deposit very high-quality silica colloidal crystal film rapidly over large areas, with a controlled thickness and without any restrictions on sphere sizes.

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