Nonhydrolytic synthesis of high-quality anisotropically shaped brookite TiO2 nanocrystals.

A surfactant-assisted nonaqueous strategy, relying on high-temperature aminolysis of titanium carboxylate complexes, has been developed to access anisotropically shaped TiO2 nanocrystals selectively trapped in the metastable brookite phase. Judicious temporal manipulation of precursor supply to the reaction mixture enables systematic tuning of the nanostructure geometric features over an exceptionally wide dimensional range (30-200 nm). Such degree of control is rationalized within the frame of a self-regulated phase-changing seed-catalyzed mechanism, in which homogeneous nucleation, on one side, and heterogeneous nucleation/growth processes, on the other side, are properly balanced while switching from the anatase to the brookite structures, respectively, in a continuous unidirectional crystal development regime. The time variation of the chemical potential for the monomer species in the solution, the size dependence of thermodynamic structural stability of the involved titania polymorphs, and the reduced activation barrier for brookite nucleation onto initially formed anatase seeds play decisive roles in the crystal-phase- and shape-tailored growth of titania nanostructures by the present approach

Determination of surface properties of various substrates using TiO2 nanorod coatings with tunable characteristics

We present a novel approach to cover different substrates with thin light-sensitive layers that consist of organic-capped TiO2 nanorods (NRs). Such NR-based coatings exhibit an increasing initial hydrophobicity with increasing NR length, and they demonstrate a surface transition from this highly hydrophobic state to a highly hydrophilic one under selective UV–laser irradiation. This behaviour is reversed under long dark storage. Infrared spectroscopy measurements reveal that light-driven wettability changes are accompanied by a progressive hydroxylation of the TiO2 surface. The surfactant molecules that cover the NRs do not appear to suffer for any significant photocatalytic degradation

The Liebherr Intelligent Hydraulic Cylinder as building block for innovative hydraulic concepts

We present hereafter the development of the Liebherr Intelligent Hydraulic Cylinder, in which the hydraulic component is used as smart sensing element providing useful information for the system in which the cylinder is operated. The piston position and velocity are the most important signals derived from this new measuring approach. The performance under various load and temperature conditions (measured both on dedicated test facilities and in field in a real machine) will be presented. An integrated control electronics, which is performing the cylinder state processing, additionally allows the synchronized acquisition of external sensors. Providing comprehensive state information, such as temperature and system pressure, advanced control techniques or monitoring functions can be realized with a monolithic device. Further developments, trends and benefits for the system architecture will be briefly analyzed and discussed

Confinement effects on optical phonons in spherical, rod-, and tetrapod-shaped nanocrystals detected by Raman spectroscopy

Spherical, rod- and tetrapod shaped CdSe nanocrystals are investigated by Raman spectroscopy and the longitudinal-optical and surface optical phonons are observed. We find that the position of the longitudinal-optical phonon slightly red-shifts with decreasing diameter, whereas the position of the surface optical phonon depends significantly on diameter and length of the rods or the tetrapod arms

Reversible Wettability Changes in Colloidal TiO2 Nanorod Thin-Film Coatings under Selective UV Laser Irradiation

We demonstrate the light-induced, reversible wettability of homogeneous nanocrystal-based, thin-film coatings composed of closely packed arrays of surfactant-capped anatase TiO2 nanorods laterally oriented on various substrates. Under selective pulsed UV laser excitation, the oxide films exhibit a surface transition from a highly hydrophobic and superoleophilic state (water and oil contact angles of 110° and less than 8°, respectively) to a highly amphiphilic condition (water and oil contact angles of 20° and 3°, respectively). A mechanism is identified according to which the UV-induced hydrophilicity correlates with a progressive increase in the degree of surface hydroxylation of TiO2. The observed wettability changes are not accompanied by any noticeable photocatalytic degradation of the surfactants on the nanorods, which has been explained by the combined effects of the intense and pulsed irradiation regime and of the rodlike nanocrystal morphology. The organic ligands on the oxide are instead assumed to rearrange conformationally in response to the lightdriven surface reconstruction. The amphiphilic state of the UV-irradiated TiO2 films is then considered as the macroscopic wetting result of alternating hydrophilic and oleophilic surface domains of nanoscale extension. Upon prolonged storage in the dark, ambient oxygen removes the newly implanted hydroxyl groups from the TiO2 surfaces and consequently affects again the conformations of ligands such that the films are allowed to recover their native hydrophobic/superoleophilic properties

Confined Optical Phonon Modes in Aligned Nanorod Arrays Detected by Resonant Inelastic Light Scattering

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