Coupling Nanowire Chemiresistors with MEMS Microhotplate Gas Sensing Platforms

Recent advances in nanotechnology have yielded materials and structures that offer great potential for improving the sensitivity, selectivity, stability, and speed of next-generation chemical gas sensors. To fabricate practical devices, the “bottom-up” approach of producing nanoscale sensing elements must be integrated with the “top-down” methodology currently dominating microtechnology. In this letter, the authors illustrate this approach by coupling a single-crystal SnO2 nanowire sensing element with a microhotplate gas sensor platform. The sensing results obtained using this prototype sensor demonstrate encouraging performance aspects including reduced operating temperature, reduced power consumption, good stability, and enhanced sensitivity

Reconstructing phase diagrams from local measurements via Gaussian processes: mapping the temperature-composition space to confidence

We show the ability to map the phase diagram of a relaxor-ferroelectric system as a function of temperature and composition through local hysteresis curve acquisition, with the voltage spectroscopy data being used as a proxy for the (unknown) microscopic state or thermodynamic parameters of materials. Given the discrete nature of the measurement points, we use Gaussian processes to reconstruct hysteresis loops in temperature and voltage space, and compare the results with the raw data and bulk dielectric spectroscopy measurements. The results indicate that the surface transition temperature is similar for all but one composition with respect to the bulk. Through clustering algorithms, we recreate the main features of the bulk diagram, and provide statistical confidence estimates for the reconstructed phase transition temperatures. We validate the method by using Gaussian processes to predict hysteresis loops for a given temperature for a composition unseen by the algorithm, and compare with measurements. These techniques can be used to map phase diagrams from functional materials in an automated fashion, and provide a method for uncertainty quantification and model selection

Ultralong Copper Phthalocyanine Nanowires with New Crystal Structure and Broad Optical Absorption

The development of molecular nanostructures plays a major role in emerging organic electronic applications, as it leads to improved performance and is compatible with our increasing need for miniaturisation. In particular, nanowires have been obtained from solution or vapour phase and have displayed high conductivity, or large interfacial areas in solar cells. In all cases however, the crystal structure remains as in films or bulk, and the exploitation of wires requires extensive post-growth manipulation as their orientations are random. Here we report copper phthalocyanine (CuPc) nanowires with diameters of 10-100 nm, high directionality and unprecedented aspect ratios. We demonstrate that they adopt a new crystal phase, designated eta-CuPc, where the molecules stack along the long axis. The resulting high electronic overlap along the centimetre length stacks achieved in our wires mediates antiferromagnetic couplings and broadens the optical absorption spectrum. The ability to fabricate ultralong, flexible metal phthalocyanine nanowires opens new possibilities for applications of these simple molecules

Effect of water adsorption on conductivity in epitaxial Sm0.1Ce0.9O2-δ thin film for micro solid oxide fuel cells applications

Water adsorption, splitting, and proton liberation were investigated on Sm0.1Ce0.9O2-δ thin films by scanning probe microscopy. An irreversible volume expansion was observed by applying a positive bias with increased temperature. The volume expansion is also linearly dependent on the relative humidity. A reversible water adsorption process and its effect on the conductivity were also investigated by electrochemical strain microscopy and first order reversal curve under a number of experiment conditions. The presence of a Ce3+ along with OH groups, detected by hard x-ray photoemission spectroscopy established a clear correlation between the water incorporation and the valence state of C