A MEMS-based solid propellant microthruster array for space and military applications

Since combustion is an easy way to achieve large quantities of energy from a small volume, we developed a MEMS based solid propellant microthruster array for small spacecraft and micro-air-vehicle applications. A thruster is composed of a fuel chamber layer, a top-side igniter with a micromachined nozzle in the same silicon layer. Layers are assembled by adhesive bonding to give final MEMS array. The thrust force is generated by the combustion of propellant stored in a few millimeter cube chamber. The micro-igniter is a polysilicon resistor deposited on a low stress SiO2/SiNx thin membrane to ensure a good heat transfer to the propellant and thus a low electric power consumption. A large range of thrust force is obtained simply by varying chamber and nozzle geometry parameters in one step of Deep Reactive Ion Etching (DRIE). Experimental tests of ignition and combustion employing home made (DB+x% BP) propellant composed of a Double-Base and Black-Powder. A temperature of 250 therefore degrees C, enough to propellant initiation, is reached for 40 mW of electric power. A combustion rate of about 3.4 mm/s is measured for DB+20% BP propellant and thrust ranges between 0.1 and 3,5 mN are obtained for BP ratio between 10% and 30% using a microthruster of 100 mu m of throat wide

Effect of MoO3 in the cathode buffer layer on the behaviour of layered organic solar cells

The behaviour of small-molecule organic solar cells based on coper-phthalocyanine/fullerene with different cathode buffer layer is investigated as a function of air exposure duration. We present the study of the effect of MoO3 on the properties of photovoltaic solar cells (OPVCs) when it is introduced in the cathode buffer layer (CBL). Photovoltaic performances were measured as a function of time of air exposure. During the first days of air exposure the efficiency of the OPVCs with MoO3 in their CBL increases significantly, while it decreases immediately after air exposure in the case of reference OPVCs, i.e. without MoO3 in the CBL. Nevertheless, the lifetime of the OPVCs with MoO3 in their CBL is around 60 days, while it is only 10 days in the case of reference OPVCs. The initial increase of the OPVC with MoO3 in their CBL is attributed to the slow decrease of the work function of MoO3 due to progressive contamination. Then, the progressive degradation of the OPVCs efficiency is due water vapour and oxygen contamination of the organic layers. The use of a double CBL, Alq3/MoO3, allows to interrupt the growth of pinholes, defects and increases the path of permeating gas. Also it can prevent the contamination of the organic layer by Al. All this results in significant increase of the lifetime of the OPVCs

Peculiarities of the stochastic motion in antiferromagnetic nanoparticles

Antiferromagnetic (AFM) materials are widely used in spintronic devices as passive elements (for stabilization of ferromangetic layers) and as active elements (for information coding). In both cases switching between the different AFM states depends in a great extent from the environmental noise. In the present paper we derive the stochastic Langevin equations for an AFM vector and corresponding Fokker-Planck equation for distribution function in the phase space of generalised coordinate and momentum. Thermal noise is modeled by a random delta-correlated magnetic field that interacts with the dynamic magnetisation of AFM particle. We analyse in details a particular case of the collinear compensated AFM in the presence of spin-polarised current. The energy distribution function for normal modes in the vicinity of two equilibrium states (static and stationary) in sub- and super-critical regimes is found. It is shown that the noise-induced dynamics of AFM vector has pecuilarities compared to that of magnetisation vector in ferromagnets.Comment: Submitted to EPJ ST, presented at the 4-th Conference on Statistical Physics, Lviv, Ukraine, 201

Solid-State NMR/Dynamic Nuclear Polarization of Polypeptides in Planar Supported Lipid Bilayers

Dynamic nuclear polarization has been developed to overcome the limitations of the inherently low signal intensity of NMR spectroscopy. This technique promises to be particularly useful for solid-state NMR spectroscopy where the signals are broadened over a larger frequency range and most investigations rely on recording low gamma nuclei. To extend the range of possible investigations, a triple-resonance flat-coil solid-state NMR probe is presented with microwave irradiation capacities allowing the investigation of static samples at temperatures of 100 K, including supported lipid bilayers. The probe performance allows for two-dimensional separated local field experiments with high-power Lee-Goldberg decoupling and cross-polarization under simultaneous irradiation from a gyrotron microwave generator. Efficient cooling of the sample turned out to be essential for best enhancements and line shape and necessitated the development of a dedicated cooling chamber. Furthermore, a new membrane-anchored biradical is presented, and the geometry of supported membranes was optimized not only for good membrane alignment, handling, stability, and filling factor of the coil but also for heat and microwave dissipation. Enhancement factors of 17-fold were obtained, and a two-dimensional PISEMA spectrum of a transmembrane helical peptide was obtained in less than 2 h

Dynamic Nuclear Polarization NMR Spectroscopy Allows High-Throughput Characterization of Microporous Organic Polymers

Dynamic nuclear polarization (DNP) solid-state NMR was used to obtain natural abundance 13C and 15N CP MAS NMR spectra of microporous organic polymers with excellent signal-to-noise ratio, allowing for unprecedented details in the molecular structure to be determined for these complex polymer networks. Sensitivity enhancements larger than 10 were obtained with bis-nitroxide radical at 14.1 T and low temperature (∼105 K). This DNP MAS NMR approach allows efficient, high-throughput characterization of libraries of porous polymers prepared by combinatorial chemistry methods