Here we report on the DNA-templated self-assembly of conducting gold nanowires between gold electrodes lithographically patterned on a silicon oxide substrate. An aqueous dispersion of 4-(dimethylamino)pyridine-stabilized gold nanoparticles was prepared. These nanoparticles recognize and bind selectively double-stranded calf thymus DNA aligned between the gold electrodes to form a linear nanoparticle array. Continuous polycrystalline gold nanowires are obtained by electroless deposition that enlarges and enjoins the individual gold nanoparticles. The above nanowires were structurally characterized using a range of electron and scanning probe microscopies and electrically characterized at room temperature using a standard probe setup. The results of these characterizations show these wires to be 20 nm high and 40 nm wide, to be continuous between interdigitated gold electrodes with an interelectrode spacing of 0.2 or 1.0 μm, and to possess a resistivity of 2 × 10-4 Ωm. These DNA-templated nanowires, the smallest reported to date, exhibit resistivities consistent with reported findings and current theory. The use of DNA as a template for the self-assembly of conducting gold nanowires represents a potentially important approach to the fabrication of nanoscale interconnects.

The controlled assembly in solution of gold nanocrystals modified by attachment of complementary protein-DNA conjugates is described. The size of the aggregates formed can be controlled by the addition of singlestranded DNA, which quickly terminates the assembly process. The rate of formation of the aggregates can also be controlled by varying the salt concentration. Consequently, two distinct regimes of aggregation kinetics are observed. At low salt concentrations, aggregation is shown to be dependent on the rate of duplex formation between the modified gold nanocrystals, i.e., reaction-limited. At higher salt concentrations, aggregation is shown to be dependent only on the rate of diffusion of the nanocrystals, i.e., diffusion-limited. The results presented provide important insights into the rates of formation of nanocrystal assemblies. Moreover, the approach adopted is modular, requiring only the relevant biotin linker chemistry to be developed for a given nanoparticle, while also precluding unfavorable interactions between the DNA and the streptavidin-coated nanoparticle. The ability to control the rate of formation and size of nanocrystal aggregates assembled is important new knowledge. Application of this knowledge will inform future studies of nanocrystal assembly in solution involving different types of nanocrystals, which is of increasing technological significance.

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