Synthesis methods, microscopy characterization and device integration of nanoscale metal oxide semiconductors for gas sensing.

A comparison is made between SnO(2), ZnO, and TiO(2) single-crystal nanowires and SnO(2) polycrystalline nanofibers for gas sensing. Both nanostructures possess a one-dimensional morphology. Different synthesis methods are used to produce these materials: thermal evaporation-condensation (TEC), controlled oxidation, and electrospinning. Advantages and limitations of each technique are listed. Practical issues associated with harvesting, purification, and integration of these materials into sensing devices are detailed. For comparison to the nascent form, these sensing materials are surface coated with Pd and Pt nanoparticles. Gas sensing tests, with respect to H(2), are conducted at ambient and elevated temperatures. Comparative normalized responses and time constants for the catalyst and noncatalyst systems provide a basis for identification of the superior metal-oxide nanostructure and catalyst combination. With temperature-dependent data, Arrhenius analyses are made to determine activation energies for the catalyst-assisted systems.

Carbon nanotube synthesis in a flame with independently prepared laser-ablated catalyst particles.

Laser ablation has been used ex situ to create metal nanoparticles for introduction into a reactive pyrolysis flame. By prior synthesis of the metal nanoparticles, the effects of the reactive gases can be clearly separated from the pyrolysis chemistry of a solvent carrier, as when nebulized solutions are used. Moreover, varying reactivity issues associated with particle growth and size are bypassed. Our results show that Fe selectively reacts with CO to produce nanotubes, whereas Ni selectively reacts with C2H2 to produce nanofibers. These observations are interpreted through the donation and withdrawal of electron density between the adsorbate's molecular orbitals and surface atoms of the metal nanoparticle. The rate of reaction of Ni with only C2H2 is found to be greater than the rate with C2H2 and CO. This suggests that CO inhibits the Ni-catalyzed reaction.

Application of laser-induced incandescence to the detection of carbon nanotubes and carbon nanofibers.

Laser-induced incandescence applied to a heterogeneous, multielement reacting flow is characterized by temporally resolved emission spectra, time-resolved emission at selected detection wavelengths, and fluence dependence. Two-pulse laser measurements are used to further probe the effects of laser-induced changes on the optical signal. Laser fluences above 0.6 J/cm2 at 1064 nm initiate laser-induced vaporization, yielding a lower incandescence intensity, as found through fluence-dependence measurements. Spectrally derived temperatures show that values of excitation laser fluence greater than this value lead to superheated plasmas with temperatures well above the vaporization point of carbon. The temporal evolution of the emission signal at these fluences is consistent with plasma dissipation processes, not incandescence from solidlike structures. Two-pulse laser experiments reveal that other material changes are produced at fluences below the apparent vaporization threshold, leading to nanostructures with different optical and thermal properties.