Spray Pyrolysis of ZnO:In: Characterization of Growth Mechanism and Interface Analysis on p-Type GaAs and n-Type Si Semiconductor Materials.

Sprayed transparent conductive oxides (TCOs) are an interesting alternative to sputtered TCOs for many applications due to the possible high throughput and a simple, atmospheric pressure process of spray deposition. In this work, the growth mechanism of sprayed ZnO:In was analyzed by transmission Kikuchi diffraction (TKD) analysis of the thin film's crystal orientation, which shows a preferred orientation of the growing grains and thus proves that the deposition occurs from the gas phase. It was observed that with increasing thickness of the layer, the average grain size increases and the measured resistivity significantly reduces to ≈5-6 × 10-3 Ω cm for layers of >500 nm thickness. Since many applications also require good electrical contact formation, the contact resistivity and the interface between sprayed IZO and n-type poly-Si and p-type GaAs, two materials that are commonly used in III-V/silicon tandem solar cells, were investigated by electrical measurements and high-resolution transmission electron microscopy (TEM) analyses. The interlayers observed in TEM were investigated by energy-dispersive X-ray spectroscopy (EDS) line scans. The results suggest that oxidic interlayers at the substrate/IZO interface are responsible for the observed higher contact resistivity compared to the contact resistivity of sputtered indium tin oxide (ITO) references. The results presented in this work lead to a better understanding of the deposition process occurring in spray pyrolysis and thus allow a more targeted optimization of process parameters depending on the future requirements of the application.

Synthesis, characterisation and water-gas shift activity of nano-particulate mixed-metal (Al, Ti) cobalt oxides.

The formation of mixed-metal cobalt oxides, representing potential metal-support compounds for cobalt-based catalysts, has been observed at high conversion levels in the Fischer-Tropsch synthesis over metal oxide-supported cobalt catalysts. An often observed increase in the carbon dioxide selectivity at Fischer-Tropsch conversion levels above 80% has been suggested to be associated to the formation of water-gas shift active oxidic cobalt species. Mixed-metal cobalt oxides, namely cobalt aluminate and cobalt titanate, were therefore synthesised and tested for potential catalytic activity in the water-gas shift reaction. We present a preparation route for amorphous mixed-metal oxides via thermal treatment of metal precursors in benzyl alcohol. Calcination of the as prepared nanoparticles results in highly crystalline phases. The nano-particulate mixed-metal cobalt oxides were thoroughly analysed by means of X-ray diffraction, Raman spectroscopy, temperature-programmed reduction, X-ray absorption near edge structure spectroscopy, extended X-ray absorption fine structure, and high-resolution scanning transmission electron microscopy. This complementary characterisation of the synthesised materials allows for a distinct identification of the phases and their properties. The cobalt aluminate prepared has a cobalt-rich composition (Co1+xAl2-xO4) with a homogeneous atomic distribution throughout the nano-particulate structures, while the perovskite-type cobalt titanate (CoTiO3) features cobalt-lean smaller particles associated with larger ones with an increased concentration of cobalt. The cobalt aluminate prepared showed no water-gas shift activity in the medium-shift temperature range, while the cobalt titanate sample catalysed the conversion of water and carbon monoxide to hydrogen and carbon dioxide after an extended activation period. However, this perovskite underwent vast restructuring forming metallic cobalt, a known catalyst for the water-gas shift reaction at temperatures exceeding typical conditions for the cobalt-based Fischer-Tropsch synthesis, and anatase-TiO2. The partial reduction of the mixed-metal oxide and segregation was identified by means of post-run characterisation using X-ray diffraction, Raman spectroscopy, and transmission electron microscopy energy-dispersive spectrometry.

Characterization of multifunctional ß-NaEuF4/NaGdF4 core-shell nanoparticles with narrow size distribution.

The properties of ß-NaEuF4/NaGdF4 core-shell nanocrystals have been thoroughly investigated. Nanoparticles with narrow size distribution and an overall diameter of ∼22 nm have been produced with either small ß-NaEuF4 cores (∼3 nm diameter) or large ß-NaEuF4 cores (∼18 nm diameter). The structural properties and core-shell formation are investigated by X-ray diffraction, transmission electron microscopy and electron paramagnetic resonance, respectively. Optical luminescence measurements and X-ray photoelectron spectroscopy are employed to gain information about the optical emission bands and valence states of the rare earth constituents. Magnetic characterization is performed by SQUID and X-ray magnetic circular dichroism measurements at the rare earth M(4,5) edges. The characterization of the core-shell nanoparticles by means of these complementary techniques demonstrates that partial intermixing of core and shell materials takes place, and a significant fraction of europium is present in the divalent state which has significant influence on the magnetic properties. Hence, we obtained a combination of red emitting Eu(3+) ions and paramagnetic Gd(3+) ions, which may be highly valuable for potential future applications.

Dynamics of single Fe atoms in graphene vacancies.

Focused electron beam irradiation has been used to create mono and divacancies in graphene within a defined area, which then act as trap sites for mobile Fe atoms initially resident on the graphene surface. Aberration-corrected transmission electron microscopy at 80 kV has been used to study the real time dynamics of Fe atoms filling the vacancy sites in graphene with atomic resolution. We find that the incorporation of a dopant atom results in pronounced displacements of the surrounding carbon atoms of up to 0.5 Å, which is in good agreement with density functional theory calculations. Once incorporated into the graphene lattice, Fe atoms can transition to adjacent lattice positions and reversibly switch their bonding between four and three nearest neighbors. The C atoms adjacent to the Fe atoms are found to be more susceptible to Stone-Wales type bond rotations with these bond rotations associated with changes in the dopant bonding configuration. These results demonstrate the use of controlled electron beam irradiation to incorporate dopants into the graphene lattice with nanoscale spatial control.

Spatial control of defect creation in graphene at the nanoscale.

Defects in graphene alter its electrical, chemical, magnetic and mechanical properties. The intentional creation of defects in graphene offers a means for engineering its properties. Techniques such as ion irradiation intentionally induce atomic defects in graphene, for example, divacancies, but these defects are randomly scattered over large distances. Control of defect formation with nanoscale precision remains a significant challenge. Here we show control over both the location and average complexity of defect formation in graphene by tailoring its exposure to a focussed electron beam. Divacancies and larger disordered structures are produced within a 10 × 10 nm(2) region of graphene and imaged after creation using an aberration-corrected transmission electron microscope. Some of the created defects were stable, whereas others relaxed to simpler structures through bond rotations and surface adatom incorporation. These results are important for the utilization of atomic defects in graphene-based research.