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This paper describes the fabrication and characterization of a hybrid nanostructure comprised of carbon nanotubes (CNTs) grown on graphene layers for supercapacitor applications. The entire nanostructure (CNTs and graphene) was fabricated via atmospheric pressure chemical vapor deposition (APCVD) and designed to minimize self-aggregation of the graphene and CNTs. Growth parameters of the CNTs were optimized by adjusting the gas flow rates of hydrogen and methane to control the simultaneous, competing reactions of carbon formation toward CNT growth and hydrogenation which suppresses CNT growth via hydrogen etching of carbon. Characterization of the supercapacitor performance of the CNT-graphene hybrid nanostructure indicated that the average measured capacitance of a fabricated graphene-CNT structure was 653.7 μF cm(-2) at 10 mV s(-1) with a standard rectangular cyclic voltammetry curve. Rapid charging-discharging characteristics (mV s(-1)) were exhibited with a capacitance of approximately 75% (490.3 μF cm(-2)). These experimental results indicate that this CNT-graphene structure has the potential towards three-dimensional (3D) graphene-CNT multi-stack structures for high-performance supercapacitors.

Zinc oxide films derived from drop-coating solutions of zinc acetate in ethanol followed by chemical bath deposition were examined for their suitability as buffer layers for high temperature vapor phase deposition of large area, aligned, zinc oxide nanorod arrays. An X-ray photoelectron spectroscopy analysis of substrates drop coated with zinc acetate solutions clarifies the chemistry of the deposition mechanism of the initial acetate-derived ZnO seeds. Scanning electron microscopy, atomic force microscopy, and white light profilometry studies show that while zinc acetate-derived buffer layers are suitable for chemical bath deposition of aligned zinc oxide nanorod arrays, during high temperature vapor phase depositions these buffer layers undergo substantial changes leading to a loss of nanorod alignment and poor substrate coverage. We present a method to deposit aligned zinc oxide nanorod arrays uniformly over large area substrates, which combines zinc acetate drop coating, chemical bath deposition of buffer layers, and vapor phase transport deposition of nanorods.

Electrospray ionization (ESI)/quadrupole ion trap mass spectrometry is used to evaluate the heavy metal binding selectivities of five caged crown ethers and two polyether reference compounds in methanol solution. The binding preferences for Hg2+, Pb2+, Cd2+, and Cu2+ were analyzed by comparison of ESI mass spectral intensities with the aim of developing this method for the rapid screening of binding selectivities of new synthetic ligands. The cage compounds preferentially bind Hg2+, except for the cage cryptand derivative, which favors Pb2+. The preference for Hg2+ stems from the favorable positioning of the nitrogen or sulfur atoms for linear coordination of Hg2+, whereas the cryptand derivative favors Pb2+ because of its larger cavity size. The counterions of the metal salts influence the type of complexes observed in the ESI mass spectra because the strengths of the metal-anion bonds affect retention of the anion in the complexes.

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