A central vision in molecular electronics is the creation of devices with functional molecular components that may provide unique properties. Proteins are attractive candidates for this purpose, as they have specific physical (optical, electrical) and chemical (selective binding, self-assembly) functions and offer a myriad of possibilities for (bio-)chemical modification. This Progress Report focuses on proteins as potential building components for future bioelectronic devices as they are quite efficient electronic conductors, compared with saturated organic molecules. The report addresses several questions: how general is this behavior; how does protein conduction compare with that of saturated and conjugated molecules; and what mechanisms enable efficient conduction across these large molecules? To answer these questions results of nanometer-scale and macroscopic electronic transport measurements across a range of organic molecules and proteins are compiled and analyzed, from single/few molecules to large molecular ensembles, and the influence of measurement methods on the results is considered. Generalizing, it is found that proteins conduct better than saturated molecules, and somewhat poorer than conjugated molecules. Significantly, the presence of cofactors (redox-active or conjugated) in the protein enhances their conduction, but without an obvious advantage for natural electron transfer proteins. Most likely, the conduction mechanisms are hopping (at higher temperatures) and tunneling (below ca. 150-200 K).

Potential future use of bacteriorhodopsin (bR) as a solid-state electron transport (ETp) material requires the highest possible active protein concentration. To that end we prepared stable monolayers of protein-enriched bR on a conducting HOPG substrate by lipid depletion of the native bR. The ETp properties of this construct were then investigated using conducting probe atomic force microscopy at low bias, both in the ground dark state and in the M-like intermediate configuration, formed upon excitation by green light. Photoconductance modulation was observed upon green and blue light excitation, demonstrating the potential of these monolayers as optoelectronic building blocks. To correlate protein structural changes with the observed behavior, measurements were made as a function of pressure under the AFM tip, as well as humidity. The junction conductance is reversible under pressure changes up to ∼300 MPa, but above this pressure the conductance drops irreversibly. ETp efficiency is enhanced significantly at >60% relative humidity, without changing the relative photoactivity significantly. These observations are ascribed to changes in protein conformation and flexibility and suggest that improved electron transport pathways can be generated through formation of a hydrogen-bonding network.

Quantum confinement effects in bismuth (Bi) nanowires (NWs) are predicted to impart them with high thermopower values and hence make them efficient thermoelectric materials. Yet, boundary scattering of charge carriers in these NWs operating in the diffusion transport regime mask any quantum effects and impede their use for nanoscale thermoelectric applications. Here we demonstrate quantum confinement effects in Bi NWs by forming in their structure ballistic quantum point contacts (QPCs) leading to exceptionally high thermopower values (S > 2 mV/K). The power factor, S(2)G, of the QPCs is maximized at G ~ 0.25G(0) (where G(0) is the quantum of conductance) within agreement with a one-band model with step edge characteristics.

Unlike their bulk counterpart, nanoparticles often show spontaneous fluctuations in their crystal structure at constant temperature [Iijima, S.; Ichihashi T. Phys. Rev. Lett.1985, 56, 616; Ajayan, P. M.; Marks L. D. Phys. Rev. Lett.1988, 60, 585; Ben-David, T.; Lereah, Y.; Deutscher, G.; Penisson, J. M.; Bourret, A.; Korman, R.; Cheyssac, P. Phys. Rev. Lett.1997, 78, 2585]. This phenomenon takes place whenever the net gain in the surface energy of the particles outweighs the energy cost of internal strain. The configurational space is then densely populated due to shallow free-energy barriers between structural local minima. Here we report that in the case of bismuth (Bi) nanoparticles (BiNPs), given the high anisotropy of the mass tensor of their charge carriers, structural fluctuations result in substantial dynamic changes in their electronic and conductance properties. Transmission electron microscopy is used to probe the stochastic dynamic structural fluctuations of selected BiNPs. The related fluctuations in the electronic band structure and conductance properties are studied by scanning tunneling spectroscopy and are shown to be temperature dependent. Continuous probing of the conductance of individual BiNPs reveals corresponding dynamic fluctuations (as high as 1 eV) in their apparent band gap. At 80 K, upon freezing of structural fluctuations, conductance anisotropy in BiNPs is detected as band gap variations as a function of tip position above individual particles. BiNPs offer a unique system to explore anisotropy in zero-dimension conductors as well as the dynamic nature of nanoparticles.

Segmented Au-Ni nanowires are demonstrated to be highly effective thermocouples with a spatial resolution of a few nanometers and a temporal resolution in the microsecond range. The performance of the devices is characterized by a self-heating procedure in which an ac heating current with frequency ω is applied on the wires while monitoring the resulting thermoelectric voltage V(TH) at 2ω using a lock-in technique. An analytical model is developed that enables one to determine the time response of the thermocouples from plots of V(TH) as a function of ω.