We have studied molecular adsorption onto stable metallic nanowires fabricated with an electrochemical method. Upon the adsorption, the quantized conductance decreases, typically, to a fractional value, which may be attributed to the scattering of the conduction electrons by the adsorbates. The further conductance change occurs when the nanowire is exposed to another molecule that has stronger adsorption strength. Because the quantized conductance is determined by a few atoms at the narrowest portion of each nanowire, adsorption of a molecule onto the portion is enough to change the conductance, which may be used for chemical sensors.

We study the electrical conductance of gold nanoconstrictions by controlling the electrochemical potential. At positive potentials, the conductance is quantized near integer multiples of G0(2e(2)/h) as shown by well-defined peaks in the conductance histogram. Below a certain potential, however, additional peaks near 0.5G(0) and 1. 5G(0) appear in the histogram. The fractional conductance steps are as stable and well defined as the integer steps. The experimental data are discussed in terms of electrochemical-potential-induced defect scattering and Fermi energy shift, but a complete theory of the phenomenon is yet to be developed.

A metallic nanowire with quantized conductance was fabricated by electrochemically etching a narrow portion of a metallic wire supported on a solid substrate down to the atomic scale. The width of the nanowire was controlled flexibly by etching atoms away or depositing atoms back onto the wire with the electrochemical potential. Using a feedback loop this method can, at will, fabricate a single or an array of long-term stable nanowires with a pre-selected quantized conductance. These stable nanowires may be used in devices as digitized conductors and as sensors that detect chemicals in the air or in solutions. Using the conductance quantization as a feedback, this method may be used to fabricate nanoelectrodes by etching off the last few atoms in the thinnest portion of each nanowire. These nanoelectrodes may be connected to single molecules in molecular devices.

We have studied the adsorption of mercaptopropionic acid, 2,2'-bipyridine, and dopamine onto electrochemically fabricated Cu nanowires. The nanowires are atomically thin with conductance quantized near integer multiples of 2e(2)/h. Upon molecular adsorption, the quantized conductance decreases to a fractional value, due to the scattering of the conduction electrons by the adsorbates. The decrease is as high as 50% for the thinnest nanowires whose conductance is at the lowest quantum step, and smaller for thicker nanowires with conductance at higher quantum steps. The adsorbate-induced conductance changes depend on the binding strengths of the molecules to the nanowires, which are in the order of mercaptopropionic acid, 2,2'-bipyridine, and dopamine, from strongest to weakest. The sensitive dependence of the quantized conductance on molecular adsorption may be used for molecular detection.

The overall conductivity of SWNT networks is dominated by the existence of high resistance and tunneling/Schottky barriers at the intertube junctions in the network. Here we report that in situ polymerization of a highly conductive self-doped conducting polymer "skin" around and along single stranded DNA dispersed and functionalized single wall carbon nanotubes can greatly decrease the contact resistance. The polymer skin also acts as "conductive glue" effectively assembling the SWNTs into a conductive network, which decreases the amount of SWNTs needed to reach the high conductive regime of the network. The conductance of the composite network after the percolation threshold can be 2 orders of magnitude higher than the network formed from SWNTs alone.