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The use of hierarchical assemblies constituted from macroporous structures (e.g., reticulated vitreous carbon, RVC) where the internal pore area is covered with closely spaced nanostructures (e.g., carbon nanotubes, CNT) is proposed for substantially enhancing the energy density of electrochemical capacitors, while maintaining large charge/discharge rates. While the macroscale pores enable storage of substantial electrolyte volumes that would contribute through redox reactions to the energy density, the closely spaced nanostructures provide a large geometric area and capacitance in addition to enabling rate independent Faradaic charge storage via thin layer electrochemistry (TLE). A fifty fold increase in the double layer capacitance, in addition to increased Faradaic charge densitywith potential for orders of magnitude improvement, was observed for the RVC-CNT electrodes, in comparison to the bare RVC foam electrode. It was seen that the hierarchical assembly enables the contribution from ~ 94% of the net volume of the wetted RVC-CNT electrode for active Faradaic charge storage.

Adsorption of chlorinated organic contaminants (COCs) on carbon nanotubes (CNTs) has been gaining ground as a remedial platform for groundwater treatment. Applications depend on our mechanistic understanding of COC adsorption on CNTs. This paper lays out the nature of competing interactions at play in hybrid, membrane, and pure CNT based systems and presents results with the perspective of existing gaps in design strategies. First, current remediation approaches to trichloroethylene (TCE), the most ubiquitous of the COCs, is presented along with examination of forces contributing to adsorption of analogous contaminants at the molecular level. Second, we present results on TCE adsorption and remediation on pure and hybrid CNT systems with a stress on the specific nature of substrate and molecular architecture that would contribute to competitive adsorption. The delineation of intermolecular interactions that contribute to efficient remediation is needed for custom, scalable field design of purification systems for a wide range of contaminants.

This paper demonstrates the effectiveness of a new type of hybrid nanocatalyst material that combines the high surface area of nanoparticles and nanotubes with the structural robustness and ease of handling larger supports. The hybrid material is made by fabricating palladium nanoparticles on two types of carbon supports: as-received microcellular foam (Foam) and foam with carbon nanotubes anchored on the pore walls (CNT/Foam). Catalytic reductive dechlorination of carbon tetrachloride with these materials has been investigated using gas chromatography. It is seen that while both palladium-functionalized carbon supports are highly effective in the degradation of carbon tetrachloride, the rate of degradation is significantly increased with palladium on CNT/Foam. However, there is scope to increase this rate further if the wettability of these structures can be enhanced in the future. Microstructural and spectroscopic analyses of the fresh and used catalysts have been compared which indicates that there is no change in density or surface chemical states of the catalyst after prolonged use in dechlorination test. This implies that these materials can be used repeatedly and hence provide a simple, powerful, and cost-effective approach for dechlorination of water.