Nicolas Siedl

Particle Networks from Powder Mixtures: Generation of TiO(2)-SnO(2) Heterojunctions via Surface Charge-Induced Heteroaggregation.

We explored the impact of interfacial property changes on aggregation behavior and photoinduced charge separation in mixed metal oxide nanoparticle ensembles. TiO2 and SnO2 nanoparticles were synthesized by metal organic chemical vapor synthesis and subsequently transformed into aqueous colloidal dispersions using formic acid for adjustment of the particles’ surface charge. Surface charge-induced heteroaggregation was found to yield blended nanoparticle systems of exceptionally high mixing quality and, after vacuum annealing, to extremely high concentrations of heterojunctions between TiO2 and SnO2 nanoparticles with dehydroxylated surfaces. For tracking charge transfer processes across heterojunctions, the photogeneration of trapped charge carriers was measured with electron paramagnetic resonance (EPR) spectroscopy. On blended nanoparticles systems with high concentrations of SnO2–TiO2 heterojunctions, we observed an enhanced cross section for interparticular charge separation. This results from an effective interfacial charge transfer across the interfaces and gives rise to substantially increased concentrations of electrons and hole centers. The here presented insights are key to the rational design of particle-based heterojunctions and mesoporous nanoparticle networks and help to engineer composite nanomaterials for photocatalysis and solar energy conversion.

Optical Properties of Nanocrystal Interfaces in Compressed MgO Nanopowders

The optical properties and charge trapping phenomena observed on oxide nanocrystal ensembles can be strongly influenced by the presence of nanocrystal interfaces. MgO powders represent a convenient system to study these effects due to the well-defined shape and controllable size distributions of MgO nanocrystals. The spectroscopic properties of nanocrystal interfaces are investigated by monitoring the dependence of absorption characteristics on the concentration of the interfaces in the nanopowders. The presence of interfaces is found to affect the absorption spectra of nanopowders more significantly than changing the size of the constituent nanocrystals and, thus, leading to the variation of the relative abundance of light-absorbing surface structures. We find a strong absorption band in the 4.0−5.5 eV energy range, which was previously attributed to surface features of individual nanocrystals, such as corners and edges. These findings are supported by complementary first-principles calculations. The possibility to directly address such interfaces by tuning the energy of excitation may provide new means for functionalization and chemical activation of nanostructures and can help improve performance and reliability for many nanopowder applications.

Synthesis and aggregation of In2O3 nanoparticles: impact of process parameters on stoichiometry changes and optical properties.

Metal-organic chemical vapor synthesis provides agglomerated In2O3 nanoparticles with a low abundance of particle-particle interfaces. Via exposure to bulk water and subsequent dehydration treatment these powders can be transformed into networks of aggregated nanoparticles. Two major effects arise from the associated emergence of particle-particle interfaces: an enhanced susceptibility to annealing induced n-type doping and a significant red-shift of the optical absorption threshold by 0.2 eV. On the basis of control experiments with pure water, we further explored the impact of the environmental gas atmosphere during annealing on the integral ensemble properties. We found that residual water vapor promotes the mutual attraction of particles, facilitates their condensation, and generates particle-particle interfaces. This work may prove to be of great value for the reproducible production and formulation of percolating metal oxide nanoparticle networks with high control over particle aggregation state, on the one hand, and n-type conductivity as well as optical properties, on the other.

Photoluminescence quenching in compressed MgO nanoparticle systems

Efficient use of highly dispersed metal oxides for lighting, energy conversion and catalysis requires knowledge about the impact of density and microstructure of the powders on the optical nanoparticle properties. For MgO nanocube powders we present a combined photoluminescence (PL) and electron paramagnetic resonance (EPR) approach which enables for samples of different aggregation states the quantification of the fractional powder volume that becomes illuminated with UV and visible light during the PL measurements. Using O2 as a PL emission quencher and - after light induced exciton separation and oxygen adsorption - as an EPR active adsorbate we observed clear aggregation dependent trends in PL emission quenching that originate from particle-particle contacts. Upon interaction of low coordinated surface elements with the surfaces of adjacent MgO nanocubes, which occurs even at powder consolidation levels that escape sorption analysis, the radiative decay of excited surface states becomes quenched down to 15% of the original intensity. Our results underline the critical role of microstructure and the aggregation state of a nanoparticle ensemble with respect to spectroscopic properties and related adsorption induced changes.

On the Entangled Growth of NaTaO3 Cubes and Na2Ti3O7 Wires in Sodium Hydroxide Solution

The entangled growth of sodium titanate Na2Ti3O7 nanowires and sodium tantalate NaTaO3 cubes was investigated with electron microscopy, X-ray diffraction, and UV diffuse reflectance spectroscopy. Depending on the composition of the Ta2O5- and TiO2-particle-based powder mixtures, which served as educts, we observed different types of hybridization effects. These include the titanium-induced contraction of the NaTaO3 perovskite-type unit cell and the generation of electronic defect states in NaTaO3 that give rise to optical subbandgap transitions and tantalum-induced limitations of the Na2Ti3O7 nanowire growth. The transformation from Ta2O5 to NaTaO3 occurs through a dissolution-recrystallization process. A systematic analysis of the impact of different titanium sources on NaTaO3 dispersion and, thus, on the properties of the entangled nanostructures revealed that a perfect intermixture of cubes and nanowires can only be achieved when titanate nanosheets emerge during transformation as reaction intermediates and shield nucleation and growth of isolated NaTaO3 cubes. The here demonstrated approach can be highly instrumental for understanding the nucleation and growth of composite and entangled nanostructures in solution and--at the same time--provides an interesting new class of photoactive composite materials.