Lorenz Kienle

Aerographite: Ultra Lightweight, Flexible Nanowall, Carbon Microtube Material with Outstanding Mechanical Performance

An ultra lightweight carbon microtube material called Aerographite is synthesized by a novel single-step chemical vapor deposition synthesis based on ZnO networks, which is presently the lightest known material with a density smaller than μg/cm(3). Despite its low density, the hierarchical design leads to remarkable mechanical, electrical, and optical properties. The first experiments with Aerographite electrodes confirm its applicability.

Direct Growth of Freestanding ZnO Tetrapod Networks for Multifunctional Applications in Photocatalysis, UV Photodetection, and Gas Sensing

Growth of freestanding nano- and microstructures with complex morphologies is a highly desired aspect for real applications of nanoscale materials in various technologies. Zinc oxide tetrapods (ZnO-T), which exhibit three-dimensional (3D) shapes, are of major importance from a technological applications point of view, and thus efficient techniques for growth of different varieties of tetrapod-based networks are demanded. Here, we demonstrate the versatile and single-step synthesis of ZnO-T with different arm morphologies by a simple flame transport synthesis (FTS) approach, forming a network. Morphological evolutions and structural intactness of these tetrapods have been investigated in detail by scanning electron microscopy, X-ray diffraction, and micro-Raman measurements. For a deeper understanding of the crystallinity, detailed high-resolution transmission electron microscopic studies on a typical ZnO tetrapod structure are presented. The involved growth mechanism for ZnO tetrapods with various arm morphologies is discussed with respect to variations in experimental conditions. These ZnO-T have been utilized for photocatalytic degradation and nanosensing applications. The photocatalytic activities of these ZnO-T with different arm morphologies forming networks have been investigated through the photocatalytic decolorization of a methylene blue (MB) solution under UV light illumination at ambient temperature. The results show that these ZnO-T exhibit strong photocatalytic activities against MB and its complete degradation can be achieved in very short time. In another application, a prototype of nanoelectronic sensing device has been built from these ZnO-T interconnected networks and accordingly utilized for UV detection and H2 gas sensing. The fabricated device structures showed excellent sensing behaviors for promising practical applications. The involved sensing mechanisms with respect to UV photons and H2 gas are discussed in detail. We consider that such multifunctional nanodevices based on ZnO tetrapod interconnected networks will be of interest for various advanced applications.

Giant Pores in a Chromium 2,6‐Naphthalenedicarboxylate Open‐Framework Structure with MIL‐101 Topology

Large, larger, ... Replacement of 1,4-benzenedicarboxylate by 2,6-naphthalenedicarboxylate in the MIL-101 structure leads to an isoreticular mesoporous framework containing cages with diameters of 39 and 46 A. High-throughput methods are employed to determine appropriate reaction conditions. The microcrystalline compound is characterized by molecular simulation techniques, powder X-ray diffraction, N(2)-sorption, and TEM investigations.

Exchange biasing of magnetoelectric composites

Magnetoelectric composite materials are promising candidates for highly sensitive magnetic-field sensors. However, the composites showing the highest reported magnetoelectric coefficients require the presence of external d.c. magnetic bias fields, which is detrimental to their use as sensitive high-resolution magnetic-field sensors. Here, we report magnetoelectric composite materials that instead rely on intrinsic magnetic fields arising from exchange bias in the device. Thin-film magnetoelectric two-two composites were fabricated by magnetron sputtering on silicon-cantilever substrates. The composites consist of piezoelectric AlN and multilayers with the sequence Ta/Cu/Mn(70)Ir(30)/Fe(50)Co(50) or Ta/Cu/Mn(70)Ir(30)/Fe(70.2)Co(7.8)Si(12)B(10) serving as the magnetostrictive component. The thickness of the ferromagnetic layers and angle dependency of the exchange bias field are used to adjust the shift of the magnetostriction curve in such a way that the maximum piezomagnetic coefficient occurs at zero magnetic bias field. These self-biased composites show high sensitivity to a.c. magnetic fields with a maximum magnetoelectric coefficient of 96 V cm(-1) Oe(-1) at mechanical resonance.

Ultralow-fatigue shape memory alloy films

Memory alloys that avoid exhaustion Shape memory alloys can pop back into shape after being deformed. However, often these alloys cannot cope with a large number of deformation cycles. Chluba et al. find an alloy that avoids this pitfall, deforming 10 million times with very little fatigue (see the Perspective by James). Such low-fatigue materials could be useful in a plethora of future applications ranging from refrigerators to artificial heart valves. Science, this issue p. 1004; see also p. 968 Precipitates that reproducibly guide the phase transformations in shape memory alloys give rise to ultralow fatigue. [Also see Perspective by James] Functional shape memory alloys need to operate reversibly and repeatedly. Quantitative measures of reversibility include the relative volume change of the participating phases and compatibility matrices for twinning. But no similar argument is known for repeatability. This is especially crucial for many future applications, such as artificial heart valves or elastocaloric cooling, in which more than 10 million transformation cycles will be required. We report on the discovery of an ultralow-fatigue shape memory alloy film system based on TiNiCu that allows at least 10 million transformation cycles. We found that these films contain Ti2Cu precipitates embedded in the base alloy that serve as sentinels to ensure complete and reproducible transformation in the course of each memory cycle.

Crystal growth behaviour in Au-ZnO nanocomposite under different annealing environments and photoswitchability

The growth of gold nanoparticles and ZnO nanorods in atom beam co-sputtered Au-ZnO nanocomposite (NC) system by annealing at two different ambient conditions is demonstrated in this work. Annealing in a furnace at 600 °C (air environment) confirmed the formation of ZnO nanorods surrounded with Au nanoparticles. In-situ annealing inside a transmission electron microscope (TEM) led to the formation of gold nanocrystals with different polygonal shapes. TEM micrographs were obtained in real time at intermediate temperatures of 300 °C, 420 °C, and 600 °C under vacuum. The growth mechanisms of Au nanocrystals and ZnO nanorods are discussed in the framework of Au-Zn eutectic and Zn-melting temperatures in vacuum and air, respectively. Current-voltage responses of Au-ZnO NC nanorods in dark as well as under light illumination have been investigated and photoswitching in Au-ZnO NC system is reported. The photoswitching has been discussed in terms of Au-ZnO band-diagram.

SnO2:Eu3+ nanoparticles dispersed in TiO2 matrix: Improved energy transfer between semiconductor host and Eu3+ ions for the low temperature synthesized samples

SnO2:Eu3+ nanoparticles uniformly dispersed in TiO2 matrix were prepared at 185°C in ethylene glycol. Unlike in SnO2:Eu3+, significant improvement in the exciton mediated energy transfer between SnO2 and Eu3+ ions was observed when SnO2:Eu3+ nanoparticles are dispersed in TiO2 matrix, and this is attributed to effective shielding of surface Eu3+ ions present in SnO2:Eu3+ nanoparticles from the vibrations of stabilizing ligand by TiO2 matrix. Annealing the samples at high temperatures leads to formation of Sn1−xTixO2, without significantly affecting the energy transfer process between Eu3+ ions and semiconductor host.

Stoichiometry of alloy nanoparticles from laser ablation of PtIr in acetone and their electrophoretic deposition on PtIr electrodes

Charged Pt-Ir alloy nanoparticles are generated through femtosecond laser ablation of a Pt₉Ir target in acetone without using chemical precursors or stabilizing agents. Preservation of the targets stoichiometry in the colloidal nanoparticles is confirmed by transmission electron microscopy (TEM)-energy-dispersive x-ray spectroscopy (EDX), high angle annular dark field (HAADF) scanning transmission electron microscopy (STEM)-EDX elemental maps, high resolution TEM and selected area electron diffraction (SAED) measurements. Results are discussed with reference to thermophysical properties and the phase diagram. The nanoparticles show a lognormal size distribution with a mean Feret particle size of 26 nm. The zeta potential of -45 mV indicates high stability of the colloid with a hydrodynamic diameter of 63 nm. The charge of the particles enables electrophoretic deposition of nanoparticles, creating nanoscale roughness on three-dimensional PtIr neural electrodes within a minute. In contrast to coating with Pt or Ir oxides, this method allows modification of the surface roughness without changing the chemical composition of PtIr.

Green chemistry and nanofabrication in a levitated Leidenfrost drop

Green nanotechnology focuses on the development of new and sustainable methods of creating nanoparticles, their localized assembly and integration into useful systems and devices in a cost-effective, simple and eco-friendly manner. Here we present our experimental findings on the use of the Leidenfrost drop as an overheated and charged green chemical reactor. Employing a droplet of aqueous solution on hot substrates, this method is capable of fabricating nanoparticles, creating nanoscale coatings on complex objects and designing porous metal in suspension and foam form, all in a levitated Leidenfrost drop. As examples of the potential applications of the Leidenfrost drop, fabrication of nanoporous black gold as a plasmonic wideband superabsorber, and synthesis of superhydrophilic and thermal resistive metal–polymer hybrid foams are demonstrated. We believe that the presented nanofabrication method may be a promising strategy towards the sustainable production of functional nanomaterials.

Defect chemistry of oxide nanomaterials with high surface area: ordered mesoporous thin films of the oxygen storage catalyst CeO2-ZrO2.

Herein we report the electrical transport properties of a series of ordered mesoporous ceria-zirconia (CexZr1-xO2, referred to as mp-CZO) thin films with both a cubic structure of (17±2) nm diameter pores and nanocrystalline walls. Samples over the whole range of composition, including bare CeO2 and ZrO2, were fabricated by templating strategies using the large diblock copolymer KLE as the structure-directing agent. Both the nanoscale structure and the chemical composition of the mesoporous materials were analyzed by a combination of scanning and transmission electron microscopy, grazing incidence small-angle X-ray scattering, X-ray photoelectron spectroscopy, and time-of-flight secondary ion mass spectrometry. The total conductivity as a function of the film composition, temperature, and oxygen partial pressure was measured using impedance spectroscopy. The mesoporous solid solutions of CeO2-ZrO2 prepared in this work showed a higher stability against thermal ripening than both binary oxides, making them ideal model systems to study both the charge transport properties and the oxygen storage at elevated temperatures. We find that the redox properties of nanocrystalline mp-CZO thin films differ significantly from those of bulk CZO materials reported in the literature and, therefore, propose a defect chemical model of surface regions.