Giant Radiolytic Dissolution Rates of Aqueous Ceria Observed in Situ by Liquid-Cell TEM.

The dynamics of cerium oxide nanoparticle aqueous corrosion are revealed in situ. We use innovative liquid-cell transmission electron microscopy (TEM) combined with deliberate high-intensity electron-beam irradiation of nanoparticle suspensions. This enables life video-recording of materials reactions in liquid, with nm resolution. We introduce image quantification to measure detailed rates of dissolution as a function of time and particle size to be compared with literature data. Giant dissolution rates, exceeding any previous reports for chemical dissolution rates at room temperature by many orders of magnitude, are discovered. The reasons for this accelerated dissolution are outlined, including the importance of the radiolysis of water preceding the ceria attack. Electron-water interaction generates radicals, ions, and hydrated electrons, which assist in hydration and reductive dissolution of oxide minerals. The presented methodology has the potential to become a novel accelerated testing procedure to compare multiple nanoscale materials for relative aqueous durability. The ceria-water system is of crucial importance for the fields of catalysis, abrasive polishing, environmental remediation, and as simulant for actinide oxide behaviour in contact with liquid for nuclear engineering.

Comparison of nanoparticular hydroxyapatite pastes of different particle content and size in a novel scapula defect model.

Nanocrystalline hydroxyapatite (HA) has good biocompatibility and the potential to support bone formation. It represents a promising alternative to autologous bone grafting, which is considered the current gold standard for the treatment of low weight bearing bone defects. The purpose of this study was to compare three bone substitute pastes of different HA content and particle size with autologous bone and empty defects, at two time points (6 and 12 months) in an ovine scapula drillhole model using micro-CT, histology and histomorphometry evaluation. The nHA-LC (38% HA content) paste supported bone formation with a high defect bridging-rate. Compared to nHA-LC, Ostim® (35% HA content) showed less and smaller particle agglomerates but also a reduced defect bridging-rate due to its fast degradation The highly concentrated nHA-HC paste (48% HA content) formed oversized particle agglomerates which supported the defect bridging but left little space for bone formation in the defect site. Interestingly, the gold standard treatment of the defect site with autologous bone tissue did not improve bone formation or defect bridging compared to the empty control. We concluded that the material resorption and bone formation was highly impacted by the particle-specific agglomeration behaviour in this study.

Engineering of nanoscale defect patterns in CeO2 nanorods via ex situ and in situ annealing.

Single-crystalline ceria nanorods were fabricated using a hydrothermal process and annealed at 325 °C-800 °C. As-synthesized CeO2 nanorods contain a high concentration of defects, such as oxygen vacancies and high lattice strains. Annealing resulted in an improved lattice crystalline quality along with the evolution of novel cavity-shaped defects in the nanorods with polyhedral morphologies and bound by e.g. {111} and {100} (internal) surfaces, confirmed for both air (ex situ) and vacuum (in situ) heating. We postulate that the cavities evolve via agglomeration of vacancies within the as-synthesized nanorods.

Mechanical properties of mesoporous ceria nanoarchitectures.

Architectural constructs are engineered to impart desirable mechanical properties facilitating bridges spanning a thousand meters and buildings nearly 1 km in height. However, do the same 'engineering-rules' translate to the nanoscale, where the architectural features are less than 0.0001 mm in size? Here, we calculate the mechanical properties of a porous ceramic functional material, ceria, as a function of its nanoarchitecture using molecular dynamics simulation and predict its yield strength to be almost two orders of magnitude higher than the parent bulk material. In particular, we generate models of nanoporous ceria with either a hexagonal or cubic array of one-dimensional pores and simulate their responses to mechanical load. We find that the mechanical properties are critically dependent upon the orientation between the crystal structure (symmetry, direction) and the pore structure (symmetry, direction).

Environment-mediated structure, surface redox activity and reactivity of ceria nanoparticles.

Nanomaterials, with potential application as bio-medicinal agents, exploit the chemical properties of a solid, with the ability to be transported (like a molecule) to a variety of bodily compartments. However, the chemical environment can change significantly the structure and hence properties of a nanomaterial. Accordingly, its surface reactivity is critically dependent upon the nature of the (biological) environment in which it resides. Here, we use Molecular Dynamics (MD) simulation, Density Functional Theory (DFT) and aberration corrected TEM to predict and rationalise differences in structure and hence surface reactivity of ceria nanoparticles in different environments. In particular we calculate reactivity 'fingerprints' for unreduced and reduced ceria nanoparticles immersed in water and in vacuum. Our simulations predict higher activities of ceria nanoparticles, towards oxygen release, when immersed in water because the water quenches the coordinative unsaturation of surface ions. Conversely, in vacuum, surface ions relax into the body of the nanoparticle to relieve coordinative unsaturation, which increases the energy barriers associated with oxygen release. Our simulations also reveal that reduced ceria nanoparticles are more active towards surface oxygen release compared to unreduced nanoceria. In parallel, experiment is used to explore the activities of ceria nanoparticles that have suffered a change in environment. In particular, we compare the ability of ceria nanoparticles, in an aqueous environment, to scavenge superoxide radicals compared to the same batch of nanoparticles, which have first been dried and then rehydrated. The latter show a distinct reduction in activity, which we correlate to a change in the redox chemistry associated with moving between different environments. The reactivity of ceria nanoparticles is therefore not only environment dependent, but is also influenced by the transport pathway or history required to reach the particular environment in which its reactivity is to be exploited.

Nanopatterning by ion implantation through nanoporous alumina masks.

The important problem of how to generate lateral order for ion implantation patterning of substrates is solved by using a nanoporous anodic alumina membrane as a mask. Co and Pt implantation is used at two implantation doses. In order to observe the achieved implantation zones free from artifacts, electron transparent thin nitride and oxide films are used as substrates, which allows the quality of pattern transfer from the mask to the thin film to be assessed by plan-view transmission electron microscopy. Characteristic density variations of implanted elements across projected pore-regions of the mask, such as ring and dome shapes, and corresponding variation of cluster size are discussed, and therefore the method also serves as a suitable test bed for ion beam focusing studies by cylindrical or conical pores.

In situ TEM observation of lithium nanoparticle growth and morphological cycling.

Lithium fluoride crystals were subjected to electron beam irradiation at 200 and 300 keV using transmission electron microscopy in order to study in situ fabrication of Li nanostructures. We observed that LiF crystals decompose in a unique way different to all other metal halides: Fluorine ablation and salt-to-metal conversion is non-local and due to a rapid lateral diffusion of Li, the life cycle from nucleation to annihilation of fresh Li nano-crystals can be observed at a distance from the Li-source, the irradiated salt. Growth, shape transition and annihilation of Li nanostructures follow at slow enough speed for live video recording with resolution of 25 frames per second. The equilibrium shapes of pure Li nano-crystals range from cubic to rod-shaped and ball-shaped and up to 300 nm size. By varying the e-beam flux of irradiation, transitions from cube to spherical shape can be induced cyclically.

Patterned ion beam implantation of Co ions into a SiO2 thin film via ordered nanoporous alumina masks.

Spatially patterned ion beam implantation of 190 keV Co(+) ions into a SiO(2) thin film on a Si substrate has been achieved by using nanoporous anodic aluminum oxide with a pore diameter of 125 nm as a mask. The successful synthesis of periodic embedded Co regions using pattern transfer is demonstrated for the first time using cross-sectional (scanning) transmission electron microscopy (TEM) in combination with analytical TEM. Implanted Co regions are found at the correct relative lateral periodicity given by the mask and at a depth of about 120 nm.

Cationic surface reconstructions on cerium oxide nanocrystals: an aberration-corrected HRTEM study.

Instabilities of nanoscale ceria surface facets are examined on the atomic level. The electron beam and its induced atom migration are proposed as a readily available probe to emulate and quantify functional surface activity, which is crucial for, for example, catalytic performance. In situ phase contrast high-resolution transmission electron microscopy with spherical aberration correction is shown to be the ideal tool to analyze cationic reconstruction. Hydrothermally prepared ceria nanoparticles with particularly enhanced {100} surface exposure are explored. Experimental analysis of cationic reconstruction is supported by molecular dynamics simulations where the Madelung energy is shown to be directly related to the binding energy, which enables one to generate a visual representation of the distribution of "reactive" surface oxygen.

A piezoelectric goniometer inside a transmission electron microscope goniometer.

Piezoelectric nanoactuators, which can provide extremely stable and reproducible positioning, are rapidly becoming the dominant means for position control in transmission electron microscopy. Here we present a second-generation miniature goniometric nanomanipulation system, which is fully piezo-actuated with ultrafine step size for translation and rotation, programmable, and can be fitted inside a hollowed standard specimen holder for a transmission electron microscope (TEM). The movement range of this miniaturized drive is composed of seven degrees of freedom: three fine translational movements (X, Y, and Z axes), three coarse translational movements along all three axes, and one rotational movement around the X-axis with an integrated angular sensor providing absolute rotation feedback. The new piezoelectric system independently operates as a goniometer inside the TEM goniometer. In situ experiments, such as tomographic tilt without missing wedge and differential tilt between two specimens, are demonstrated.

In-situ fabrication of three dimensional nickel nanobeads by electron beam induced transformation.

We report an in-situ transmission electron microscope method for the fabrication of three dimensional nickel nanobeads. Conversion of nickel fluoride into a three dimensional porous, partially fluorine depleted aggregate is shown as intermediate state, followed by transformation into metallic beads. The bead size ranges from 10-600 nm and can be controlled via materials thickness and beam intensity. The material is found sensitive for the formation of nickel dots, rings and lines by focused exposure with various beam shapes.

Mechanical properties of ceria nanorods and nanochains; the effect of dislocations, grain-boundaries and oriented attachment.

We predict that the presence of extended defects can reduce the mechanical strength of a ceria nanorod by 70%. Conversely, the pristine material can deform near its theoretical strength limit. Specifically, atomistic models of ceria nanorods have been generated with full microstructure, including: growth direction, morphology, surface roughening (steps, edges, corners), point defects, dislocations and grain-boundaries. The models were then used to calculate the mechanical strength as a function of microstructure. Our simulations reveal that the compressive yield strengths of ceria nanorods, ca. 10 nm in diameter and without extended defects, are 46 and 36 GPa for rods oriented along [211] and [110] respectively, which represents almost 10% of the bulk elastic modulus and are associated with yield strains of about 0.09. Tensile yield strengths were calculated to be about 50% lower with associated yield strains of about 0.06. For both nanorods, plastic deformation was found to proceed via slip in the {001} plane with direction <110>--a primary slip system for crystals with the fluorite structure. Dislocation evolution for the nanorod oriented along [110] was nucleated via a cerium vacancy present at the surface. A nanorod oriented along [321] and comprising twin-grain boundaries with {111} interfacial planes was calculated to have a yield strength of about 10 GPa (compression and tension) with the grain boundary providing the vehicle for plastic deformation, which slipped in the plane of the grain boundary, with an associated <110> slip direction. We also predict, using a combination of atomistic simulation and DFT, that rutile-structured ceria is feasible when the crystal is placed under tension. The mechanical properties of nanochains, comprising individual ceria nanoparticles with oriented attachment and generated using simulated self-assembly, were found to be similar to those of the nanorod with grain-boundary. Images of the atom positions during tension and compression are shown, together with animations, revealing the mechanisms underpinning plastic deformation. For the nanochain, our simulations help further our understanding of how a crystallising ice front can be used to 'sculpt' ceria nanoparticles into nanorods via oriented attachment.

Conductive nichrome probe tips: fabrication, characterization and application as nanotools.

Conductive nichrome probe tips have been developed as functionalized nanotools for nanoscale electrical testing and nanowelding. The apex size and shape of the ultra-sharp probes is controllable and reproducible. Structural and chemical characterization have been systematically carried out. The conductive quality of these tips has been demonstrated using them for nanoscale electrical testing and as a nanotool for nanowelding, indicating that they can easily form remarkable low resistance ohmic contacts. Nichrome tips should have a wide application as nanotools in nanotechnology, and be advantageous in competition with other scanning probe tips because of their unique combination of high resistance to oxidation, high hardness and relatively high resistivity.

Mapping nanostructure: a systematic enumeration of nanomaterials by assembling nanobuilding blocks at crystallographic positions.

Nanomaterials synthesized from nanobuilding blocks promise size-dependent properties, associated with individual nanoparticles, together with collective properties of ordered arrays. However, one cannot position nanoparticles at specific locations; rather innovative ways of coaxing these particles to self-assemble must be devised. Conversely, model nanoparticles can be placed in any desired position, which enables a systematic enumeration of nanostructure from model nanobuilding blocks. This is desirable because a list of chemically feasible hypothetical structures will help guide the design of strategies leading to their synthesis. Moreover, the models can help characterize nanostructure, calculate (predict) properties, or simulate processes. Here, we start to formulate and use a simulation strategy to generate atomistic models of nanomaterials, which can, potentially, be synthesized from nanobuilding block precursors. Clearly, this represents a formidable task because the number of ways nanoparticles can be arranged into a superlattice is infinite. Nevertheless, numerical tools are available to help build nanoparticle arrays in a systematic way. Here, we exploit the "rules of crystallography" and position nanoparticles, rather than atoms, at crystallographic sites. Specifically, we explore nanoparticle arrays with cubic, tetragonal, and hexagonal symmetries together with primitive, face centered cubic and body centered cubic nanoparticle "packing". We also explore binary nanoparticle superlattices. The resulting nanomaterials, spanning CeO(2), Ti-doped CeO(2), ZnO, ZnS, MgO, CaO, SrO, and BaO, comprise framework architectures, with cavities interconnected by channels traversing (zero), one, two and three dimensions. The final, fully atomistic models comprise three hierarchical levels of structural complexity: crystal structure, microstructure (i.e., grain boundaries, dislocations), and superlattice structure.

IMAGE-WARP: a real-space restoration method for high-resolution STEM images using quantitative HRTEM analysis.

We have developed a new method for processing distorted high-resolution scanning transmission electron microscopy (STEM) images. The method is based on finding the displaced vertices in the experimental STEM image and warping to geometrically correct reference grid of the object. As a reference grid for warping a structural model obtained using a high-resolution transmission electron microscopy (HRTEM) analysis of the area of interest is utilised. Combined with quantitative HRTEM analysis the IMAGE-WARP method provides a real-space restoration of high-resolution high-angle annular dark-field (HAADF) STEM images without affecting the original Z-contrast information. The method can be applied to extract valuable compositional atomic-column data from any HAADF-STEM image of any kind of bulk crystals with local occupancy or chemistry fluctuations, stacking faults, special grain boundaries or interfaces, for which we have an available structural model. After the warping, distortion-corrected images can be further enhanced using conventional image-filtering techniques, and finally quantified with HAADF-STEM image simulations. The applicability of the IMAGE-WARP method was illustrated using experimental HAADF-STEM images of a strontium titanate crystal disrupted with a Ruddlesden-Popper-type antiphase boundary.

Nanobeam propagation and imaging in a FEGTEM/STEM.

Atomic resolution information by EELS can only be obtained by careful control of the propagation and spreading of the beam within the sample. A multislice calculation is used to estimate 3D-intensity distributions in sapphire illuminated with beams of 0.1-0.3 nm diameter, with the focus, Cs-value, and specimen thickness as the variables. The 3D-intensity pattern is then used to predict spatially resolved ELNES signals, interpreted as a convolution of the atomically projected density of states (DOS) with an elastic excitation envelope. The site-and-momentum projected DOS functions are calculated using local density function theory, applied to a rhombohedral grain boundary in sapphire. Finally, experimental difficulties in directly imaging the beam exit wave of a nanobeam-illuminated specimen are demonstrated. Calculation and experiments are for a typical modern high-resolution 300 kV FEGTEM.

Spectroscopic electron tomography.

The elemental mapping techniques in analytical transmission electron microscopy (TEM), energy filtered imaging (EFTEM) and EDX-mapping, are shown to provide new routes for tomographic reconstructions of 3D chemical maps on the nanoscale. The inelastic scattering does not only provide chemical sensitivity but also improves the linear projection relationship between mass density and image intensity, which often fails in bright field TEM of crystalline materials due to diffraction contrast. Instrumental requirements and artefact sources within the contrast formation mechanisms and within the numerical reconstruction are assessed.